Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 32 |
|---|---|
| ensemblid | ENSG00000076555.16 |
| hgncid | 85 |
| symbol | ACACB |
| name | acetyl-CoA carboxylase beta |
| refseq_nuc | NM_001093.4 |
| refseq_prot | NP_001084.3 |
| ensembl_nuc | ENST00000338432.12 |
| ensembl_prot | ENSP00000341044.7 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 109116587 |
| end | 109268226 |
| strand | + |
| ver | v1.2 |
| region | chr12:109116587-109268226 |
| region5000 | chr12:109111587-109273226 |
| regionname0 | ACACB_chr12_109116587_109268226 |
| regionname5000 | ACACB_chr12_109111587_109273226 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 2458 | 121 | 41 | 16 | 44 | 8 | 12 | 31 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002 | 1/0 | 2458 | 55 | 14 | 5 | 24 | 0 | 11 | 13 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0003 | 0/0 | 2458 | 34 | 0 | 6 | 26 | 1 | 1 | 16 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0004 | 0/0 | 2458 | 12 | 0 | 2 | 9 | 0 | 1 | 7 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0005 | 0/0 | 2458 | 12 | 0 | 1 | 9 | 0 | 2 | 9 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006 | 0/0 | 2458 | 11 | 6 | 1 | 3 | 1 | 0 | 2 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0007 | 0/1 | 2458 | 8 | 7 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0008 | 0/0 | 2458 | 7 | 6 | 0 | 1 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0009 | 0/0 | 2458 | 6 | 2 | 4 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0010 | 0/0 | 2458 | 4 | 0 | 1 | 1 | 0 | 2 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0011 | 0/0 | 2458 | 3 | 0 | 2 | 1 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0012 | 0/0 | 2458 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0013 | 0/0 | 2458 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0014 | 0/0 | 2458 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0015 | 0/0 | 2458 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0016 | 0/0 | 2458 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0017 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0018 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0019 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0020 | 0/0 | 2458 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0021 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0022 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0023 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0024 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0025 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0026 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0027 | 0/0 | 2458 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0028 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0029 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0030 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0031 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0032 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0033 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0034 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0035 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0036 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0037 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0038 | 0/0 | 2458 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0039 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0040 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0041 | 0/0 | 2458 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 7377 | 22 | 0 | 4 | 18 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0002 | 0/0 | 7377 | 18 | 4 | 5 | 8 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0003 | 0/0 | 7377 | 15 | 3 | 1 | 5 | 1 | 5 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0004 | 0/0 | 7377 | 12 | 2 | 0 | 10 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0005 | 0/0 | 7377 | 10 | 0 | 1 | 8 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0006 | 0/0 | 7377 | 9 | 3 | 2 | 2 | 0 | 2 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0007 | 1/0 | 7377 | 8 | 5 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0008 | 0/0 | 7377 | 7 | 0 | 1 | 6 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0009 | 0/0 | 7377 | 7 | 0 | 0 | 7 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0010 | 0/0 | 7377 | 5 | 2 | 0 | 3 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0011 | 0/0 | 7377 | 5 | 2 | 0 | 1 | 1 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0012 | 0/0 | 7377 | 5 | 0 | 0 | 5 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0013 | 0/0 | 7377 | 5 | 0 | 0 | 4 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0014 | 0/0 | 7377 | 5 | 0 | 0 | 1 | 0 | 4 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0015 | 0/0 | 7377 | 5 | 5 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0016 | 0/0 | 7377 | 4 | 4 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0017 | 0/0 | 7377 | 4 | 2 | 0 | 1 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0018 | 0/0 | 7377 | 4 | 0 | 4 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0019 | 0/0 | 7377 | 4 | 0 | 1 | 2 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0020 | 0/0 | 7377 | 4 | 0 | 0 | 3 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0021 | 0/0 | 7377 | 4 | 0 | 0 | 4 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0022 | 0/0 | 7377 | 4 | 4 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0023 | 0/0 | 7377 | 4 | 0 | 2 | 0 | 2 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0024 | 0/0 | 7377 | 4 | 0 | 1 | 3 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0025 | 0/0 | 7377 | 4 | 0 | 4 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0026 | 0/0 | 7377 | 3 | 0 | 0 | 2 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0027 | 0/0 | 7377 | 3 | 0 | 2 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0028 | 0/0 | 7377 | 3 | 0 | 0 | 3 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0029 | 0/0 | 7377 | 3 | 1 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0030 | 0/1 | 7377 | 3 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0031 | 0/0 | 7377 | 3 | 3 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0032 | 0/0 | 7377 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0033 | 0/0 | 7377 | 2 | 0 | 2 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0034 | 0/0 | 7377 | 2 | 0 | 0 | 0 | 2 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0035 | 0/0 | 7377 | 2 | 0 | 0 | 0 | 0 | 2 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0036 | 0/0 | 7377 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0037 | 0/0 | 7377 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0038 | 0/0 | 7377 | 2 | 1 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0039 | 0/0 | 7377 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0040 | 0/0 | 7377 | 2 | 0 | 0 | 1 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0041 | 0/0 | 7377 | 2 | 0 | 1 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0042 | 0/0 | 7377 | 2 | 0 | 1 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0043 | 0/0 | 7377 | 2 | 0 | 0 | 1 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0044 | 0/0 | 7377 | 2 | 1 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0045 | 0/0 | 7377 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0046 | 0/0 | 7377 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0047 | 0/0 | 7377 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0048 | 0/0 | 7377 | 2 | 1 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0049 | 0/0 | 7377 | 2 | 1 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0050 | 0/0 | 7377 | 2 | 0 | 1 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0051 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0052 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0053 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0054 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0055 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0056 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0057 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0058 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0059 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0060 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0061 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0062 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0063 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0064 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0065 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0066 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0067 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0068 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0069 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0070 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0071 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0072 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0073 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0074 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0075 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0076 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0077 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0078 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0079 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0080 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0081 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0082 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0083 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0084 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0085 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0086 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0087 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0088 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0089 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0090 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0091 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0092 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0093 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0094 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0095 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0096 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0097 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0098 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0099 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0100 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0101 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0102 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0103 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0104 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0105 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0106 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0107 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0108 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0109 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0110 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0111 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0112 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0113 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0114 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0115 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0116 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0117 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0118 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0119 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0120 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0121 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0122 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0123 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| c0124 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1995 | 81 | 14 | 19 | 36 | 7 | 5 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0002 | 0/1 | 1993 | 64 | 8 | 7 | 36 | 2 | 10 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0003 | 1/0 | 1992 | 57 | 5 | 8 | 27 | 0 | 16 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0004 | 0/0 | 1994 | 39 | 29 | 3 | 4 | 0 | 3 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0005 | 0/0 | 1993 | 12 | 11 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0006 | 0/0 | 1992 | 9 | 0 | 0 | 9 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0007 | 0/0 | 1970 | 7 | 0 | 0 | 7 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0008 | 0/0 | 1996 | 6 | 0 | 0 | 6 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0009 | 0/0 | 1994 | 6 | 6 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0010 | 0/0 | 1992 | 4 | 4 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0011 | 0/0 | 1994 | 4 | 1 | 2 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0012 | 0/0 | 1993 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0013 | 0/0 | 1994 | 2 | 1 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0014 | 0/0 | 1993 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0015 | 0/0 | 1993 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0016 | 0/0 | 1992 | 2 | 0 | 1 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0017 | 0/0 | 1994 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0018 | 0/0 | 1994 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0019 | 0/0 | 1993 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0020 | 0/0 | 1969 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0021 | 0/0 | 1995 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0022 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0023 | 0/0 | 1993 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0024 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| t0025 | 0/0 | 1994 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 7377 | 18 | 4 | 5 | 8 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0003 | 0/0 | 7377 | 15 | 3 | 1 | 5 | 1 | 5 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0004 | 0/0 | 7377 | 12 | 2 | 0 | 10 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0010 | 0/0 | 7377 | 5 | 2 | 0 | 3 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0011 | 0/0 | 7377 | 5 | 2 | 0 | 1 | 1 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0012 | 0/0 | 7377 | 5 | 0 | 0 | 5 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0013 | 0/0 | 7377 | 5 | 0 | 0 | 4 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0016 | 0/0 | 7377 | 4 | 4 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0018 | 0/0 | 7377 | 4 | 0 | 4 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0022 | 0/0 | 7377 | 4 | 4 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0023 | 0/0 | 7377 | 4 | 0 | 2 | 0 | 2 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0029 | 0/0 | 7377 | 3 | 1 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0032 | 0/0 | 7377 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0034 | 0/0 | 7377 | 2 | 0 | 0 | 0 | 2 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0038 | 0/0 | 7377 | 2 | 1 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0039 | 0/0 | 7377 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0045 | 0/0 | 7377 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0046 | 0/0 | 7377 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0048 | 0/0 | 7377 | 2 | 1 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0049 | 0/0 | 7377 | 2 | 1 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0050 | 0/0 | 7377 | 2 | 0 | 1 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0054 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0055 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0058 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0060 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0062 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0064 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0069 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0074 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0087 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0089 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0095 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0098 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0105 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0106 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0107 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0108 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0109 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0111 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0124 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0006 | 0/0 | 7377 | 9 | 3 | 2 | 2 | 0 | 2 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0007 | 1/0 | 7377 | 8 | 5 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0014 | 0/0 | 7377 | 5 | 0 | 0 | 1 | 0 | 4 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0017 | 0/0 | 7377 | 4 | 2 | 0 | 1 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0020 | 0/0 | 7377 | 4 | 0 | 0 | 3 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0021 | 0/0 | 7377 | 4 | 0 | 0 | 4 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0024 | 0/0 | 7377 | 4 | 0 | 1 | 3 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0028 | 0/0 | 7377 | 3 | 0 | 0 | 3 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0036 | 0/0 | 7377 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0043 | 0/0 | 7377 | 2 | 0 | 0 | 1 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0053 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0061 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0070 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0086 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0088 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0092 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0097 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0110 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0117 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0118 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0003c0001 | 0/0 | 7377 | 22 | 0 | 4 | 18 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0003c0005 | 0/0 | 7377 | 10 | 0 | 1 | 8 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0003c0081 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0003c0083 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0004c0008 | 0/0 | 7377 | 7 | 0 | 1 | 6 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0004c0040 | 0/0 | 7377 | 2 | 0 | 0 | 1 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0004c0041 | 0/0 | 7377 | 2 | 0 | 1 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0004c0112 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0005c0009 | 0/0 | 7377 | 7 | 0 | 0 | 7 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0005c0019 | 0/0 | 7377 | 4 | 0 | 1 | 2 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0005c0056 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0026 | 0/0 | 7377 | 3 | 0 | 0 | 2 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0031 | 0/0 | 7377 | 3 | 3 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0078 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0113 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0120 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0121 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0122 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0007c0030 | 0/1 | 7377 | 3 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0007c0037 | 0/0 | 7377 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0007c0057 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0007c0101 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0007c0104 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0008c0015 | 0/0 | 7377 | 5 | 5 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0008c0044 | 0/0 | 7377 | 2 | 1 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0009c0025 | 0/0 | 7377 | 4 | 0 | 4 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0009c0096 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0009c0103 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0010c0042 | 0/0 | 7377 | 2 | 0 | 1 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0010c0073 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0010c0075 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0011c0027 | 0/0 | 7377 | 3 | 0 | 2 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0012c0035 | 0/0 | 7377 | 2 | 0 | 0 | 0 | 0 | 2 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0013c0033 | 0/0 | 7377 | 2 | 0 | 2 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0014c0077 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0014c0079 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0015c0114 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0015c0119 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0016c0047 | 0/0 | 7377 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0017c0123 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0018c0051 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0019c0093 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0020c0052 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0021c0068 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0022c0084 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0023c0099 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0024c0091 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0025c0090 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0026c0066 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0027c0065 | 0/0 | 7377 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0028c0100 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0029c0085 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0030c0071 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0031c0067 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0032c0059 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0033c0063 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0034c0102 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0035c0076 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0036c0094 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0037c0072 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0038c0082 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0039c0080 | 0/0 | 7377 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0040c0115 | 0/0 | 7377 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0041c0116 | 0/0 | 7377 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 9371 | 16 | 4 | 5 | 6 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0002t0008 | 0/0 | 9372 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0002t0021 | 0/0 | 9371 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0003t0002 | 0/0 | 9369 | 13 | 1 | 1 | 5 | 1 | 5 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0003t0004 | 0/0 | 9370 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0004t0002 | 0/0 | 9369 | 3 | 1 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0004t0007 | 0/0 | 9346 | 7 | 0 | 0 | 7 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0004t0017 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0004t0020 | 0/0 | 9345 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0010t0001 | 0/0 | 9371 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0010t0002 | 0/0 | 9369 | 3 | 0 | 0 | 3 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0010t0009 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0011t0001 | 0/0 | 9371 | 4 | 2 | 0 | 0 | 1 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0011t0008 | 0/0 | 9372 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0012t0002 | 0/0 | 9369 | 5 | 0 | 0 | 5 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0013t0001 | 0/0 | 9371 | 5 | 0 | 0 | 4 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0016t0009 | 0/0 | 9370 | 3 | 3 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0016t0011 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0018t0002 | 0/0 | 9369 | 2 | 0 | 2 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0018t0011 | 0/0 | 9370 | 2 | 0 | 2 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0022t0004 | 0/0 | 9370 | 4 | 4 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0023t0001 | 0/0 | 9371 | 3 | 0 | 1 | 0 | 2 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0023t0004 | 0/0 | 9370 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0029t0002 | 0/0 | 9369 | 2 | 1 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0029t0011 | 0/0 | 9370 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0032t0004 | 0/0 | 9370 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0034t0001 | 0/0 | 9371 | 2 | 0 | 0 | 0 | 2 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0038t0001 | 0/0 | 9371 | 2 | 1 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0039t0004 | 0/0 | 9370 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0045t0002 | 0/0 | 9369 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0046t0002 | 0/0 | 9369 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0048t0002 | 0/0 | 9369 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0048t0004 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0049t0001 | 0/0 | 9371 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0049t0004 | 0/0 | 9370 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0050t0001 | 0/0 | 9371 | 2 | 0 | 1 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0054t0001 | 0/0 | 9371 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0055t0001 | 0/0 | 9371 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0058t0016 | 0/0 | 9368 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0060t0002 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0062t0019 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0064t0009 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0069t0002 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0074t0004 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0087t0001 | 0/0 | 9371 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0089t0002 | 0/0 | 9369 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0095t0001 | 0/0 | 9371 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0098t0001 | 0/0 | 9371 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0105t0004 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0106t0001 | 0/0 | 9371 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0107t0012 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0108t0001 | 0/0 | 9371 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0109t0002 | 0/0 | 9369 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0111t0001 | 0/0 | 9371 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0001c0124t0012 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0006t0003 | 0/0 | 9368 | 5 | 0 | 2 | 1 | 0 | 2 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0006t0005 | 0/0 | 9369 | 3 | 3 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0006t0014 | 0/0 | 9369 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0007t0003 | 1/0 | 9368 | 6 | 4 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0007t0006 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0007t0022 | 0/0 | 9368 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0014t0003 | 0/0 | 9368 | 5 | 0 | 0 | 1 | 0 | 4 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0017t0003 | 0/0 | 9368 | 3 | 1 | 0 | 1 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0017t0024 | 0/0 | 9368 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0020t0003 | 0/0 | 9368 | 4 | 0 | 0 | 3 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0021t0003 | 0/0 | 9368 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0021t0006 | 0/0 | 9368 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0024t0003 | 0/0 | 9368 | 4 | 0 | 1 | 3 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0028t0003 | 0/0 | 9368 | 3 | 0 | 0 | 3 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0036t0003 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0036t0006 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0043t0003 | 0/0 | 9368 | 2 | 0 | 0 | 1 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0053t0005 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0061t0003 | 0/0 | 9368 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0070t0005 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0086t0003 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0088t0006 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0092t0010 | 0/0 | 9368 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0097t0003 | 0/0 | 9368 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0110t0003 | 0/0 | 9368 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0117t0003 | 0/0 | 9368 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0002c0118t0005 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0003c0001t0001 | 0/0 | 9371 | 19 | 0 | 4 | 15 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0003c0001t0004 | 0/0 | 9370 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0003c0001t0008 | 0/0 | 9372 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0003c0005t0002 | 0/0 | 9369 | 10 | 0 | 1 | 8 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0003c0081t0002 | 0/0 | 9369 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0003c0083t0001 | 0/0 | 9371 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0004c0008t0001 | 0/0 | 9371 | 4 | 0 | 1 | 3 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0004c0008t0008 | 0/0 | 9372 | 3 | 0 | 0 | 3 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0004c0040t0002 | 0/0 | 9369 | 2 | 0 | 0 | 1 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0004c0041t0002 | 0/0 | 9369 | 2 | 0 | 1 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0004c0112t0001 | 0/0 | 9371 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0005c0009t0003 | 0/0 | 9368 | 4 | 0 | 0 | 4 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0005c0009t0006 | 0/0 | 9368 | 3 | 0 | 0 | 3 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0005c0019t0003 | 0/0 | 9368 | 3 | 0 | 1 | 1 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0005c0019t0006 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0005c0056t0003 | 0/0 | 9368 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0026t0002 | 0/0 | 9369 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0026t0016 | 0/0 | 9368 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0031t0004 | 0/0 | 9370 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0031t0013 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0078t0001 | 0/0 | 9371 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0113t0004 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0120t0003 | 0/0 | 9368 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0121t0004 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0006c0122t0004 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0007c0030t0002 | 0/1 | 9369 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0007c0030t0004 | 0/0 | 9370 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0007c0037t0004 | 0/0 | 9370 | 2 | 2 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0007c0057t0004 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0007c0101t0002 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0007c0104t0004 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0008c0015t0005 | 0/0 | 9369 | 5 | 5 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0008c0044t0003 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0008c0044t0025 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0009c0025t0001 | 0/0 | 9371 | 4 | 0 | 4 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0009c0096t0009 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0009c0103t0004 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0010c0042t0003 | 0/0 | 9368 | 2 | 0 | 1 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0010c0073t0014 | 0/0 | 9369 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0010c0075t0003 | 0/0 | 9368 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0011c0027t0004 | 0/0 | 9370 | 2 | 0 | 1 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0011c0027t0013 | 0/0 | 9370 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0012c0035t0004 | 0/0 | 9370 | 2 | 0 | 0 | 0 | 0 | 2 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0013c0033t0002 | 0/0 | 9369 | 2 | 0 | 2 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0014c0077t0004 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0014c0079t0004 | 0/0 | 9370 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0015c0114t0004 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0015c0119t0004 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0016c0047t0002 | 0/0 | 9369 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0017c0123t0015 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0018c0051t0023 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0019c0093t0001 | 0/0 | 9371 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0020c0052t0001 | 0/0 | 9371 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0021c0068t0001 | 0/0 | 9371 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0022c0084t0004 | 0/0 | 9370 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0023c0099t0001 | 0/0 | 9371 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0024c0091t0002 | 0/0 | 9369 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0025c0090t0003 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0026c0066t0015 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0027c0065t0005 | 0/0 | 9369 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0028c0100t0001 | 0/0 | 9371 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0029c0085t0003 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0030c0071t0002 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0031c0067t0003 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0032c0059t0002 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0033c0063t0010 | 0/0 | 9368 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0034c0102t0018 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0035c0076t0010 | 0/0 | 9368 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0036c0094t0004 | 0/0 | 9370 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0037c0072t0001 | 0/0 | 9371 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0038c0082t0002 | 0/0 | 9369 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0039c0080t0010 | 0/0 | 9368 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0040c0115t0001 | 0/0 | 9371 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| a0041c0116t0003 | 0/0 | 9368 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | copy fasta | chr12 | 109111587 | 109273226 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0002t0021g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0003t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0004t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0004t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0004t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0004t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0004t0007g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0004t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0004t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0004t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0004t0007g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0004t0017g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0004t0020g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0010t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0010t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0010t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0010t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0010t0009g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0011t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0011t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0011t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0011t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0011t0008g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0012t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0012t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0012t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0012t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0012t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0013t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0013t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0013t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0013t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0013t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0016t0009g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0016t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0016t0009g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0016t0011g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0018t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0018t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0018t0011g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0018t0011g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0022t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0022t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0022t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0022t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0023t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0023t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0023t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0023t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0029t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0029t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0029t0011g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0032t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0032t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0034t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0034t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0038t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0038t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0039t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0039t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0045t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0045t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0046t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0046t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0048t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0048t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0049t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0049t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0050t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0050t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0054t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0055t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0058t0016g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0060t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0062t0019g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0064t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0069t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0074t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0087t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0089t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0095t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0098t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0105t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0106t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0107t0012g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0108t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0109t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0111t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0001c0124t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0006t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0006t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0006t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0006t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0006t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0006t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0006t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0006t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0006t0014g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0007t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0007t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0007t0003g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0007t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0007t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0007t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0007t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0007t0022g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0014t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0014t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0014t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0014t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0014t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0017t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0017t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0017t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0017t0024g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0020t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0020t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0020t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0020t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0021t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0021t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0021t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0021t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0024t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0024t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0024t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0024t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0028t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0028t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0028t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0036t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0036t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0043t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0043t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0053t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0061t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0070t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0086t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0088t0006g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0092t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0097t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0110t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0117t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0002c0118t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0001t0008g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0005t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0005t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0005t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0005t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0005t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0005t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0005t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0005t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0005t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0005t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0081t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0003c0083t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0004c0008t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0004c0008t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0004c0008t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0004c0008t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0004c0008t0008g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0004c0008t0008g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0004c0008t0008g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0004c0040t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0004c0040t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0004c0041t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0004c0041t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0004c0112t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0005c0009t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0005c0009t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0005c0009t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0005c0009t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0005c0009t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0005c0009t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0005c0009t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0005c0019t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0005c0019t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0005c0019t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0005c0019t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0005c0056t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0006c0026t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0006c0026t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0006c0026t0016g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0006c0031t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0006c0031t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0006c0031t0013g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0006c0078t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0006c0113t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0006c0120t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0006c0121t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0006c0122t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0007c0030t0002g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0007c0030t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0007c0030t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0007c0037t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0007c0037t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0007c0057t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0007c0101t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0007c0104t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0008c0015t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0008c0015t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0008c0015t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0008c0015t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0008c0015t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0008c0044t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0008c0044t0025g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0009c0025t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0009c0025t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0009c0025t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0009c0025t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0009c0096t0009g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0009c0103t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0010c0042t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0010c0042t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0010c0073t0014g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0010c0075t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0011c0027t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0011c0027t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0011c0027t0013g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0012c0035t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0012c0035t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0013c0033t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0013c0033t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0014c0077t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0014c0079t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0015c0114t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0015c0119t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0016c0047t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0016c0047t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0017c0123t0015g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0018c0051t0023g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0019c0093t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0020c0052t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0021c0068t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0022c0084t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0023c0099t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0024c0091t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0025c0090t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0026c0066t0015g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0027c0065t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0028c0100t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0029c0085t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0030c0071t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0031c0067t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0032c0059t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0033c0063t0010g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0034c0102t0018g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0035c0076t0010g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0036c0094t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0037c0072t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0038c0082t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0039c0080t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0040c0115t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| a0041c0116t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0034 | t0001 | g0212 | EUR | GBR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0085 | EUR | GBR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00280 | hp1 | a0001 | c0034 | t0001 | g0211 | EUR | FIN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00280 | hp2 | a0001 | c0013 | t0001 | g0256 | EUR | FIN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00323 | hp1 | a0006 | c0026 | t0016 | g0066 | EUR | FIN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00323 | hp2 | a0001 | c0011 | t0001 | g0008 | EUR | FIN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00408 | hp1 | a0024 | c0091 | t0002 | g0174 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00408 | hp2 | a0003 | c0005 | t0002 | g0246 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00423 | hp1 | a0001 | c0012 | t0002 | g0262 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00423 | hp2 | a0002 | c0006 | t0014 | g0080 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00438 | hp1 | a0001 | c0003 | t0002 | g0097 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00438 | hp2 | a0001 | c0087 | t0001 | g0236 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00544 | hp1 | a0001 | c0013 | t0001 | g0163 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00544 | hp2 | a0002 | c0088 | t0006 | g0247 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00558 | hp1 | a0002 | c0036 | t0006 | g0223 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00558 | hp2 | a0002 | c0006 | t0003 | g0111 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00597 | hp1 | a0001 | c0004 | t0002 | g0052 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00609 | hp1 | a0002 | c0028 | t0003 | g0160 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00609 | hp2 | a0003 | c0001 | t0001 | g0137 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00621 | hp1 | a0002 | c0021 | t0006 | g0255 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00621 | hp2 | a0003 | c0005 | t0002 | g0245 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00639 | hp1 | a0003 | c0005 | t0002 | g0060 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00639 | hp2 | a0002 | c0006 | t0003 | g0095 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00642 | hp1 | a0002 | c0006 | t0003 | g0092 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00642 | hp2 | a0004 | c0008 | t0001 | g0221 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00673 | hp1 | a0001 | c0029 | t0002 | g0096 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00673 | hp2 | a0003 | c0001 | t0001 | g0147 | EAS | CHS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00735 | hp1 | a0005 | c0019 | t0003 | g0152 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00735 | hp2 | a0001 | c0023 | t0004 | g0121 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG00741 | hp2 | a0003 | c0001 | t0001 | g0143 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01069 | hp1 | a0009 | c0025 | t0001 | g0270 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01069 | hp2 | a0003 | c0001 | t0001 | g0064 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01070 | hp2 | a0001 | c0018 | t0002 | g0048 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01074 | hp1 | a0001 | c0050 | t0001 | g0277 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01074 | hp2 | a0009 | c0025 | t0001 | g0105 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01081 | hp1 | a0027 | c0065 | t0005 | g0225 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01106 | hp1 | a0003 | c0001 | t0001 | g0138 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01106 | hp2 | a0009 | c0025 | t0001 | g0301 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01109 | hp1 | a0003 | c0083 | t0001 | g0151 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01109 | hp2 | a0006 | c0120 | t0003 | g0043 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01167 | hp1 | a0010 | c0042 | t0003 | g0220 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01167 | hp2 | a0001 | c0058 | t0016 | g0187 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01168 | hp1 | a0013 | c0033 | t0002 | g0189 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01168 | hp2 | a0011 | c0027 | t0013 | g0065 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01169 | hp1 | a0004 | c0041 | t0002 | g0222 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01169 | hp2 | a0013 | c0033 | t0002 | g0185 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01175 | hp1 | a0001 | c0111 | t0001 | g0275 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0193 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01192 | hp2 | a0003 | c0001 | t0001 | g0178 | AMR | PUR | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01255 | hp1 | a0002 | c0024 | t0003 | g0302 | AMR | CLM | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01255 | hp2 | a0001 | c0018 | t0011 | g0047 | AMR | CLM | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01258 | hp1 | a0002 | c0097 | t0003 | g0124 | AMR | CLM | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01258 | hp2 | a0009 | c0025 | t0001 | g0269 | AMR | CLM | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0081 | AMR | CLM | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01261 | hp2 | a0011 | c0027 | t0004 | g0150 | AMR | CLM | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01433 | hp1 | a0014 | c0079 | t0004 | g0180 | AMR | CLM | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01433 | hp2 | a0001 | c0018 | t0002 | g0049 | AMR | CLM | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01515 | hp1 | a0003 | c0005 | t0002 | g0059 | EUR | IBS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01515 | hp2 | a0001 | c0023 | t0001 | g0100 | EUR | IBS | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01884 | hp1 | a0017 | c0123 | t0015 | g0058 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01884 | hp2 | a0002 | c0007 | t0003 | g0055 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01891 | hp1 | a0001 | c0074 | t0004 | g0229 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01891 | hp2 | a0034 | c0102 | t0018 | g0195 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01943 | hp1 | a0002 | c0110 | t0003 | g0268 | AMR | PEL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01943 | hp2 | a0001 | c0054 | t0001 | g0203 | AMR | PEL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02015 | hp1 | a0002 | c0086 | t0003 | g0260 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02015 | hp2 | a0031 | c0067 | t0003 | g0027 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02027 | hp1 | a0002 | c0028 | t0003 | g0228 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02040 | hp1 | a0003 | c0005 | t0002 | g0264 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02040 | hp2 | a0003 | c0001 | t0001 | g0158 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02056 | hp1 | a0029 | c0085 | t0003 | g0238 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02056 | hp2 | a0003 | c0001 | t0001 | g0149 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02071 | hp1 | a0004 | c0008 | t0001 | g0227 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02071 | hp2 | a0002 | c0043 | t0003 | g0012 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02074 | hp1 | a0001 | c0011 | t0008 | g0018 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02074 | hp2 | a0004 | c0112 | t0001 | g0119 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02080 | hp1 | a0001 | c0003 | t0002 | g0244 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02080 | hp2 | a0022 | c0084 | t0004 | g0254 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02083 | hp1 | a0001 | c0004 | t0007 | g0022 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02083 | hp2 | a0003 | c0001 | t0001 | g0265 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02132 | hp1 | a0025 | c0090 | t0003 | g0130 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02132 | hp2 | a0003 | c0005 | t0002 | g0129 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02145 | hp1 | a0007 | c0101 | t0002 | g0086 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02145 | hp2 | a0007 | c0037 | t0004 | g0200 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02257 | hp1 | a0001 | c0039 | t0004 | g0116 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0075 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02258 | hp1 | a0002 | c0118 | t0005 | g0231 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02280 | hp1 | a0008 | c0015 | t0005 | g0172 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02280 | hp2 | a0001 | c0064 | t0009 | g0184 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02523 | hp1 | a0006 | c0026 | t0002 | g0156 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02523 | hp2 | a0002 | c0024 | t0003 | g0093 | EAS | KHV | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02572 | hp1 | a0002 | c0007 | t0003 | g0037 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02572 | hp2 | a0002 | c0006 | t0005 | g0284 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02615 | hp1 | a0030 | c0071 | t0002 | g0040 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02622 | hp1 | a0001 | c0039 | t0004 | g0039 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02622 | hp2 | a0007 | c0030 | t0004 | g0285 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02630 | hp1 | a0001 | c0011 | t0001 | g0056 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0283 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02698 | hp1 | a0002 | c0117 | t0003 | g0125 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02698 | hp2 | a0010 | c0042 | t0003 | g0209 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02717 | hp1 | a0001 | c0010 | t0009 | g0186 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02717 | hp2 | a0001 | c0038 | t0001 | g0201 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02723 | hp1 | a0001 | c0095 | t0001 | g0133 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02723 | hp2 | a0001 | c0010 | t0001 | g0188 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02738 | hp1 | a0002 | c0006 | t0003 | g0107 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02738 | hp2 | a0003 | c0081 | t0002 | g0230 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02809 | hp1 | a0006 | c0031 | t0004 | g0002 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02809 | hp2 | a0009 | c0103 | t0004 | g0165 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02818 | hp1 | a0008 | c0015 | t0005 | g0173 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02818 | hp2 | a0002 | c0006 | t0005 | g0123 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02896 | hp1 | a0001 | c0032 | t0004 | g0292 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02896 | hp2 | a0002 | c0017 | t0024 | g0044 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02897 | hp1 | a0006 | c0122 | t0004 | g0167 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02897 | hp2 | a0001 | c0032 | t0004 | g0291 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02922 | hp1 | a0001 | c0011 | t0001 | g0157 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02922 | hp2 | a0036 | c0094 | t0004 | g0072 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02965 | hp1 | a0001 | c0016 | t0011 | g0274 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02965 | hp2 | a0006 | c0121 | t0004 | g0170 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02970 | hp1 | a0001 | c0049 | t0001 | g0289 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02970 | hp2 | a0008 | c0015 | t0005 | g0057 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02976 | hp1 | a0001 | c0105 | t0004 | g0296 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02976 | hp2 | a0001 | c0062 | t0019 | g0288 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03017 | hp1 | a0002 | c0020 | t0003 | g0273 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03017 | hp2 | a0012 | c0035 | t0004 | g0063 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03041 | hp1 | a0002 | c0006 | t0005 | g0294 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03041 | hp2 | a0006 | c0031 | t0004 | g0206 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03098 | hp1 | a0001 | c0098 | t0001 | g0286 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03098 | hp2 | a0035 | c0076 | t0010 | g0267 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03130 | hp1 | a0001 | c0004 | t0017 | g0003 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03130 | hp2 | a0008 | c0044 | t0025 | g0166 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03139 | hp1 | a0001 | c0022 | t0004 | g0006 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03139 | hp2 | a0001 | c0016 | t0009 | g0287 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03195 | hp1 | a0039 | c0080 | t0010 | g0071 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03195 | hp2 | a0002 | c0007 | t0022 | g0032 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03209 | hp1 | a0001 | c0107 | t0012 | g0196 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03209 | hp2 | a0001 | c0106 | t0001 | g0293 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03225 | hp1 | a0032 | c0059 | t0002 | g0038 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03225 | hp2 | a0033 | c0063 | t0010 | g0117 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03239 | hp1 | a0001 | c0049 | t0004 | g0088 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03239 | hp2 | a0001 | c0109 | t0002 | g0276 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03453 | hp1 | a0001 | c0003 | t0004 | g0300 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03453 | hp2 | a0006 | c0031 | t0013 | g0205 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03486 | hp1 | a0001 | c0016 | t0009 | g0305 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03486 | hp2 | a0007 | c0104 | t0004 | g0183 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03490 | hp1 | a0002 | c0014 | t0003 | g0303 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03490 | hp2 | a0001 | c0003 | t0002 | g0112 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03492 | hp1 | a0001 | c0038 | t0001 | g0029 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03492 | hp2 | a0002 | c0014 | t0003 | g0113 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03516 | hp1 | a0021 | c0068 | t0001 | g0202 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03516 | hp2 | a0008 | c0015 | t0005 | g0168 | AFR | ESN | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03540 | hp1 | a0007 | c0057 | t0004 | g0207 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03540 | hp2 | a0002 | c0007 | t0003 | g0041 | AFR | GWD | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03579 | hp1 | a0001 | c0003 | t0004 | g0074 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03579 | hp2 | a0002 | c0092 | t0010 | g0192 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03654 | hp1 | a0010 | c0075 | t0003 | g0214 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03654 | hp2 | a0038 | c0082 | t0002 | g0127 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03669 | hp1 | a0002 | c0061 | t0003 | g0062 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03669 | hp2 | a0001 | c0003 | t0002 | g0104 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03704 | hp1 | a0041 | c0116 | t0003 | g0069 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03704 | hp2 | a0020 | c0052 | t0001 | g0210 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03710 | hp1 | a0001 | c0048 | t0002 | g0281 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03710 | hp2 | a0001 | c0003 | t0002 | g0103 | SAS | PJL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03831 | hp1 | a0002 | c0017 | t0003 | g0025 | SAS | BEB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03831 | hp2 | a0004 | c0040 | t0002 | g0213 | SAS | BEB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03834 | hp1 | a0002 | c0043 | t0003 | g0051 | SAS | BEB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03834 | hp2 | a0001 | c0003 | t0002 | g0094 | SAS | BEB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG04115 | hp1 | a0001 | c0011 | t0001 | g0013 | SAS | STU | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG04115 | hp2 | a0002 | c0006 | t0003 | g0194 | SAS | STU | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG04184 | hp1 | a0002 | c0014 | t0003 | g0083 | SAS | BEB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG04184 | hp2 | a0012 | c0035 | t0004 | g0082 | SAS | BEB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG04199 | hp1 | a0005 | c0019 | t0003 | g0135 | SAS | STU | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG04199 | hp2 | a0001 | c0108 | t0001 | g0010 | SAS | STU | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG04204 | hp1 | a0005 | c0056 | t0003 | g0053 | SAS | STU | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0078 | SAS | STU | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18522 | hp1 | a0002 | c0070 | t0005 | g0199 | AFR | YRI | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18522 | hp2 | a0015 | c0114 | t0004 | g0009 | AFR | YRI | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18612 | hp1 | a0002 | c0024 | t0003 | g0034 | EAS | CHB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18612 | hp2 | a0001 | c0004 | t0007 | g0001 | EAS | CHB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18747 | hp1 | a0003 | c0005 | t0002 | g0134 | EAS | CHB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18747 | hp2 | a0001 | c0012 | t0002 | g0045 | EAS | CHB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18906 | hp1 | a0001 | c0069 | t0002 | g0204 | AFR | YRI | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18906 | hp2 | a0002 | c0017 | t0003 | g0042 | AFR | YRI | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18942 | hp1 | a0005 | c0009 | t0003 | g0061 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18942 | hp2 | a0001 | c0004 | t0007 | g0001 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18945 | hp1 | a0001 | c0010 | t0002 | g0016 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18945 | hp2 | a0003 | c0001 | t0001 | g0140 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18946 | hp1 | a0003 | c0001 | t0001 | g0154 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18946 | hp2 | a0004 | c0040 | t0002 | g0215 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18947 | hp1 | a0001 | c0013 | t0001 | g0237 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18947 | hp2 | a0003 | c0005 | t0002 | g0131 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18950 | hp1 | a0001 | c0002 | t0021 | g0243 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18950 | hp2 | a0023 | c0099 | t0001 | g0084 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18951 | hp1 | a0001 | c0003 | t0002 | g0102 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18951 | hp2 | a0003 | c0001 | t0001 | g0132 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18952 | hp1 | a0002 | c0020 | t0003 | g0233 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18952 | hp2 | a0001 | c0004 | t0007 | g0020 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18959 | hp1 | a0001 | c0046 | t0002 | g0067 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18959 | hp2 | a0003 | c0005 | t0002 | g0240 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18960 | hp1 | a0005 | c0009 | t0003 | g0164 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18960 | hp2 | a0001 | c0029 | t0011 | g0090 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18961 | hp1 | a0003 | c0001 | t0001 | g0298 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18961 | hp2 | a0005 | c0009 | t0006 | g0148 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18962 | hp1 | a0001 | c0045 | t0002 | g0146 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18962 | hp2 | a0005 | c0009 | t0006 | g0257 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18963 | hp1 | a0005 | c0009 | t0003 | g0144 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18963 | hp2 | a0001 | c0004 | t0007 | g0019 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18966 | hp1 | a0001 | c0013 | t0001 | g0153 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18966 | hp2 | a0011 | c0027 | t0004 | g0249 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18970 | hp1 | a0004 | c0008 | t0008 | g0216 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18970 | hp2 | a0001 | c0089 | t0002 | g0162 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18974 | hp1 | a0016 | c0047 | t0002 | g0175 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18974 | hp2 | a0001 | c0002 | t0008 | g0306 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18979 | hp1 | a0003 | c0001 | t0001 | g0136 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18979 | hp2 | a0001 | c0012 | t0002 | g0251 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18980 | hp2 | a0001 | c0004 | t0020 | g0023 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18981 | hp1 | a0004 | c0008 | t0001 | g0218 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18981 | hp2 | a0002 | c0021 | t0006 | g0239 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18983 | hp1 | a0003 | c0001 | t0004 | g0266 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18983 | hp2 | a0001 | c0012 | t0002 | g0250 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18984 | hp1 | a0002 | c0007 | t0006 | g0017 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18984 | hp2 | a0004 | c0008 | t0001 | g0198 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18987 | hp1 | a0001 | c0003 | t0002 | g0077 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18987 | hp2 | a0001 | c0010 | t0002 | g0261 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18988 | hp2 | a0001 | c0012 | t0002 | g0259 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18992 | hp1 | a0010 | c0073 | t0014 | g0208 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18992 | hp2 | a0008 | c0044 | t0003 | g0182 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18993 | hp1 | a0003 | c0001 | t0001 | g0141 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18993 | hp2 | a0001 | c0004 | t0002 | g0050 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18994 | hp1 | a0001 | c0045 | t0002 | g0234 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18994 | hp2 | a0002 | c0017 | t0003 | g0024 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18995 | hp1 | a0002 | c0036 | t0003 | g0161 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18995 | hp2 | a0001 | c0004 | t0007 | g0011 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18998 | hp1 | a0001 | c0013 | t0001 | g0248 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18998 | hp2 | a0001 | c0046 | t0002 | g0190 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19003 | hp1 | a0001 | c0010 | t0002 | g0021 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19003 | hp2 | a0028 | c0100 | t0001 | g0070 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19004 | hp1 | a0003 | c0001 | t0001 | g0142 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19004 | hp2 | a0001 | c0004 | t0007 | g0028 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19009 | hp1 | a0002 | c0021 | t0003 | g0253 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19009 | hp2 | a0006 | c0026 | t0002 | g0155 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19010 | hp1 | a0019 | c0093 | t0001 | g0159 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19010 | hp2 | a0002 | c0007 | t0003 | g0026 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19011 | hp1 | a0003 | c0001 | t0001 | g0297 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19011 | hp2 | a0004 | c0008 | t0008 | g0263 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19012 | hp1 | a0003 | c0005 | t0002 | g0299 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19012 | hp2 | a0004 | c0041 | t0002 | g0224 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19030 | hp1 | a0001 | c0022 | t0004 | g0007 | AFR | LWK | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19030 | hp2 | a0006 | c0113 | t0004 | g0031 | AFR | LWK | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19043 | hp1 | a0018 | c0051 | t0023 | g0279 | AFR | LWK | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19043 | hp2 | a0001 | c0048 | t0004 | g0307 | AFR | LWK | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19057 | hp1 | a0003 | c0001 | t0004 | g0139 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19057 | hp2 | a0002 | c0024 | t0003 | g0036 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19060 | hp1 | a0003 | c0001 | t0001 | g0087 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19060 | hp2 | a0006 | c0078 | t0001 | g0181 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19063 | hp1 | a0002 | c0014 | t0003 | g0015 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19063 | hp2 | a0002 | c0021 | t0003 | g0252 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19066 | hp1 | a0003 | c0001 | t0001 | g0145 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19066 | hp2 | a0005 | c0009 | t0003 | g0304 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19068 | hp1 | a0002 | c0020 | t0003 | g0120 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19068 | hp2 | a0003 | c0001 | t0008 | g0128 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19074 | hp1 | a0004 | c0008 | t0008 | g0219 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19074 | hp2 | a0016 | c0047 | t0002 | g0176 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19080 | hp2 | a0005 | c0009 | t0006 | g0177 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19084 | hp1 | a0040 | c0115 | t0001 | g0258 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19084 | hp2 | a0005 | c0019 | t0006 | g0076 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19085 | hp1 | a0037 | c0072 | t0001 | g0217 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19085 | hp2 | a0002 | c0028 | t0003 | g0179 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19091 | hp1 | a0001 | c0003 | t0002 | g0099 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19091 | hp2 | a0002 | c0020 | t0003 | g0232 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19240 | hp1 | a0001 | c0022 | t0004 | g0005 | AFR | YRI | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA19240 | hp2 | a0002 | c0053 | t0005 | g0033 | AFR | YRI | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA20129 | hp1 | a0009 | c0096 | t0009 | g0295 | AFR | ASW | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA20129 | hp2 | a0001 | c0055 | t0001 | g0226 | AFR | ASW | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA20752 | hp1 | a0001 | c0023 | t0001 | g0122 | EUR | TSI | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0068 | EUR | TSI | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA20905 | hp1 | a0001 | c0050 | t0001 | g0278 | SAS | GIH | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA20905 | hp2 | a0002 | c0014 | t0003 | g0106 | SAS | GIH | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01123 | hp1 | a0001 | c0018 | t0011 | g0046 | AMR | CLM | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG01123 | hp2 | a0001 | c0023 | t0001 | g0089 | AMR | CLM | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02109 | hp1 | a0001 | c0060 | t0002 | g0272 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02109 | hp2 | a0001 | c0016 | t0009 | g0290 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02486 | hp1 | a0008 | c0015 | t0005 | g0171 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02486 | hp2 | a0007 | c0030 | t0004 | g0280 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02559 | hp1 | a0015 | c0119 | t0004 | g0169 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG02559 | hp2 | a0026 | c0066 | t0015 | g0115 | AFR | ACB | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03471 | hp1 | a0014 | c0077 | t0004 | g0118 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG03471 | hp2 | a0001 | c0004 | t0002 | g0054 | AFR | MSL | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG06807 | hp1 | a0002 | c0007 | t0003 | g0014 | AFR | USA | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| HG06807 | hp2 | a0007 | c0037 | t0004 | g0073 | AFR | USA | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18955 | hp1 | a0005 | c0019 | t0003 | g0271 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA20300 | hp1 | a0001 | c0029 | t0002 | g0108 | AFR | USA | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA20300 | hp2 | a0001 | c0124 | t0012 | g0197 | AFR | USA | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA21309 | hp1 | a0001 | c0003 | t0002 | g0101 | AFR | LWK | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| NA21309 | hp2 | a0001 | c0022 | t0004 | g0004 | AFR | LWK | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| homoSapiens_chm13v2 | hp1 | a0007 | c0030 | t0002 | g0110 | REF | REF | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| homoSapiens_grch38 | hp1 | a0002 | c0007 | t0003 | g0030 | REF | REF | ACACB_chr12_109111587_109273226 | ACACB | chr12 | 109111587 | 109273226 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109139533
|
C | T | 1 | a0017 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.128C>T | p.Pro43Leu | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/53 | 255/9368 | 128/7377 | 43/2458 | chr12 | 109139533 | ||
| chr12:109139668
|
G | A | 1 | a0018 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.263G>A | p.Arg88Gln | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/53 | 390/9368 | 263/7377 | 88/2458 | chr12 | 109139668 | ||
| chr12:109166863
|
C | T | 1 | a0019 | 1 | NA19010.hp1 | missense_variant&splice_region_variant | MODERATE | c.656C>T | p.Pro219Leu | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/53 | 783/9368 | 656/7377 | 219/2458 | chr12 | 109166863 | ||
| chr12:109171822
|
G | T | 1 | a0041 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.943G>T | p.Asp315Tyr | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 5/53 | 1070/9368 | 943/7377 | 315/2458 | chr12 | 109171822 | ||
| chr12:109174182
|
G | A | 1 | a0020 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.1168G>A | p.Val390Ile | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/53 | 1295/9368 | 1168/7377 | 390/2458 | chr12 | 109174182 | ||
| chr12:109174201
|
A | G | 1 | a0040 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.1187A>G | p.Gln396Arg | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/53 | 1314/9368 | 1187/7377 | 396/2458 | chr12 | 109174201 | ||
| chr12:109176021
|
A | G | 1 | a0016 | 2 | NA18974.hp1 NA19074.hp2 |
missense_variant | MODERATE | c.1307A>G | p.Asp436Gly | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 8/53 | 1434/9368 | 1307/7377 | 436/2458 | chr12 | 109176021 | ||
| chr12:109179923
|
A | G | 4 | a0006a0008a0014others(1): Show | 22 | HG00323.hp1 HG01109.hp2 HG01433.hp1 others(19): Show |
missense_variant | MODERATE | c.1654A>G | p.Ile552Val | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/53 | 1781/9368 | 1654/7377 | 552/2458 | chr12 | 109179923 | ||
| chr12:109185711
|
G | A | 6 | a0003a0005a0011others(3): Show | 53 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
missense_variant | MODERATE | c.1951G>A | p.Ala651Thr | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/53 | 2078/9368 | 1951/7377 | 651/2458 | chr12 | 109185711 | ||
| chr12:109197029
|
A | G | 5 | a0004a0010a0020others(2): Show | 19 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
missense_variant | MODERATE | c.2503A>G | p.Met835Val | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/53 | 2630/9368 | 2503/7377 | 835/2458 | chr12 | 109197029 | ||
| chr12:109222889
|
C | G | 1 | a0021 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.3769C>G | p.Gln1257Glu | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 26/53 | 3896/9368 | 3769/7377 | 1257/2458 | chr12 | 109222889 | ||
| chr12:109227385
|
G | C | 1 | a0037 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.3897G>C | p.Arg1299Ser | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/53 | 4024/9368 | 3897/7377 | 1299/2458 | chr12 | 109227385 | ||
| chr12:109227437
|
G | A | 6 | a0009a0033a0034others(3): Show | 11 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(8): Show |
missense_variant | MODERATE | c.3949G>A | p.Gly1317Ser | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/53 | 4076/9368 | 3949/7377 | 1317/2458 | chr12 | 109227437 | ||
| chr12:109237187
|
G | A | 1 | a0022 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.4469G>A | p.Arg1490His | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/53 | 4596/9368 | 4469/7377 | 1490/2458 | chr12 | 109237187 | ||
| chr12:109239924
|
G | A | 1 | a0023 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.4757G>A | p.Arg1586His | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 35/53 | 4884/9368 | 4757/7377 | 1586/2458 | chr12 | 109239924 | ||
| chr12:109241093
|
C | T | 1 | a0024 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.4834C>T | p.Arg1612Cys | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/53 | 4961/9368 | 4834/7377 | 1612/2458 | chr12 | 109241093 | ||
| chr12:109241132
|
C | T | 1 | a0025 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.4873C>T | p.Leu1625Phe | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/53 | 5000/9368 | 4873/7377 | 1625/2458 | chr12 | 109241132 | ||
| chr12:109245728
|
C | T | 1 | a0026 | 1 | HG02559.hp2 | stop_gained | HIGH | c.5281C>T | p.Arg1761* | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 38/53 | 5408/9368 | 5281/7377 | 1761/2458 | chr12 | 109245728 | ||
| chr12:109246239
|
G | A | 1 | a0027 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.5362G>A | p.Val1788Met | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/53 | 5489/9368 | 5362/7377 | 1788/2458 | chr12 | 109246239 | ||
| chr12:109246269
|
C | G | 1 | a0033 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.5392C>G | p.Arg1798Gly | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/53 | 5519/9368 | 5392/7377 | 1798/2458 | chr12 | 109246269 | ||
| chr12:109246320
|
G | A | 5 | a0007a0015a0021others(2): Show | 13 | HG02145.hp1 HG02145.hp2 HG02486.hp2 others(10): Show |
missense_variant | MODERATE | c.5443G>A | p.Glu1815Lys | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/53 | 5570/9368 | 5443/7377 | 1815/2458 | chr12 | 109246320 | ||
| chr12:109253037
|
C | T | 1 | a0028 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.5924C>T | p.Thr1975Ile | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 43/53 | 6051/9368 | 5924/7377 | 1975/2458 | chr12 | 109253037 | ||
| chr12:109253060
|
G | A | 1 | a0029 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.5947G>A | p.Val1983Ile | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 43/53 | 6074/9368 | 5947/7377 | 1983/2458 | chr12 | 109253060 | ||
| chr12:109254248
|
C | T | 6 | a0007a0011a0012others(3): Show | 18 | HG01168.hp2 HG01261.hp2 HG01433.hp1 others(15): Show |
missense_variant | MODERATE | c.6080C>T | p.Thr2027Ile | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/53 | 6207/9368 | 6080/7377 | 2027/2458 | chr12 | 109254248 | ||
| chr12:109254256
|
A | G | 1 | a0036 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.6088A>G | p.Ile2030Val | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/53 | 6215/9368 | 6088/7377 | 2030/2458 | chr12 | 109254256 | ||
| chr12:109259033
|
G | A | 28 | a0001a0003a0004others(25): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
missense_variant | MODERATE | c.6421G>A | p.Val2141Ile | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/53 | 6548/9368 | 6421/7377 | 2141/2458 | chr12 | 109259033 | ||
| chr12:109262460
|
G | A | 1 | a0013 | 2 | HG01168.hp1 HG01169.hp2 |
missense_variant | MODERATE | c.6778G>A | p.Glu2260Lys | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/53 | 6905/9368 | 6778/7377 | 2260/2458 | chr12 | 109262460 | ||
| chr12:109264361
|
G | A | 1 | a0030 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.6917G>A | p.Arg2306Gln | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 50/53 | 7044/9368 | 6917/7377 | 2306/2458 | chr12 | 109264361 | ||
| chr12:109265135
|
G | A | 1 | a0034 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.6968G>A | p.Arg2323His | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 51/53 | 7095/9368 | 6968/7377 | 2323/2458 | chr12 | 109265135 | ||
| chr12:109265153
|
G | A | 1 | a0031 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.6986G>A | p.Arg2329His | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 51/53 | 7113/9368 | 6986/7377 | 2329/2458 | chr12 | 109265153 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109139424
|
C | T | 1 | a0001c0124 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.19C>T | p.Leu7Leu | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/53 | 146/9368 | 19/7377 | 7/2458 | chr12 | 109139424 | ||
| chr12:109139660
|
C | T | 7 | a0002c0118a0006c0031a0006c0120others(4): Show | 13 | HG01109.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
synonymous_variant | LOW | c.255C>T | p.Ala85Ala | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/53 | 382/9368 | 255/7377 | 85/2458 | chr12 | 109139660 | ||
| chr12:109139679
|
C | T | 1 | a0002c0117 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.274C>T | p.Leu92Leu | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/53 | 401/9368 | 274/7377 | 92/2458 | chr12 | 109139679 | ||
| chr12:109139930
|
C | T | 37 | a0001c0002a0001c0003a0001c0023others(34): Show | 96 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(93): Show |
synonymous_variant | LOW | c.525C>T | p.Ser175Ser | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/53 | 652/9368 | 525/7377 | 175/2458 | chr12 | 109139930 | ||
| chr12:109167925
|
C | T | 28 | a0001c0012a0001c0013a0001c0022others(25): Show | 91 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
synonymous_variant | LOW | c.816C>T | p.Ala272Ala | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/53 | 943/9368 | 816/7377 | 272/2458 | chr12 | 109167925 | ||
| chr12:109179243
|
T | G | 5 | a0001c0054a0001c0055a0001c0095others(2): Show | 5 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
synonymous_variant | LOW | c.1593T>G | p.Val531Val | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 10/53 | 1720/9368 | 1593/7377 | 531/2458 | chr12 | 109179243 | ||
| chr12:109180060
|
T | C | 73 | a0001c0002a0001c0003a0001c0012others(70): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
synonymous_variant | LOW | c.1791T>C | p.Asp597Asp | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/53 | 1918/9368 | 1791/7377 | 597/2458 | chr12 | 109180060 | ||
| chr12:109185671
|
C | G | 1 | a0035c0076 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.1911C>G | p.Thr637Thr | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/53 | 2038/9368 | 1911/7377 | 637/2458 | chr12 | 109185671 | ||
| chr12:109188073
|
C | T | 1 | a0001c0108 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.2055C>T | p.Ser685Ser | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/53 | 2182/9368 | 2055/7377 | 685/2458 | chr12 | 109188073 | ||
| chr12:109188097
|
C | T | 1 | a0010c0075 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.2079C>T | p.His693His | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/53 | 2206/9368 | 2079/7377 | 693/2458 | chr12 | 109188097 | ||
| chr12:109191652
|
C | T | 31 | a0001c0002a0001c0003a0001c0018others(28): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
synonymous_variant | LOW | c.2184C>T | p.Gly728Gly | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 14/53 | 2311/9368 | 2184/7377 | 728/2458 | chr12 | 109191652 | ||
| chr12:109199429
|
G | A | 2 | a0001c0022a0014c0077 | 5 | HG03139.hp1 HG03471.hp1 NA19030.hp1 others(2): Show |
synonymous_variant | LOW | c.2655G>A | p.Thr885Thr | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/53 | 2782/9368 | 2655/7377 | 885/2458 | chr12 | 109199429 | ||
| chr12:109199429
|
G | T | 3 | a0006c0113a0014c0079a0015c0114 | 3 | HG01433.hp1 NA18522.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.2655G>T | p.Thr885Thr | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/53 | 2782/9368 | 2655/7377 | 885/2458 | chr12 | 109199429 | ||
| chr12:109206811
|
C | T | 22 | a0001c0022a0001c0039a0001c0055others(19): Show | 30 | HG00323.hp1 HG01433.hp1 HG01891.hp1 others(27): Show |
synonymous_variant | LOW | c.3015C>T | p.Asn1005Asn | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/53 | 3142/9368 | 3015/7377 | 1005/2458 | chr12 | 109206811 | ||
| chr12:109234033
|
C | T | 1 | a0021c0068 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.4335C>T | p.Phe1445Phe | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/53 | 4462/9368 | 4335/7377 | 1445/2458 | chr12 | 109234033 | ||
| chr12:109237224
|
T | C | 85 | a0001c0002a0001c0003a0001c0010others(82): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
synonymous_variant | LOW | c.4506T>C | p.Leu1502Leu | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/53 | 4633/9368 | 4506/7377 | 1502/2458 | chr12 | 109237224 | ||
| chr12:109237242
|
C | T | 1 | a0019c0093 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.4524C>T | p.Phe1508Phe | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/53 | 4651/9368 | 4524/7377 | 1508/2458 | chr12 | 109237242 | ||
| chr12:109237251
|
C | T | 1 | a0021c0068 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.4533C>T | p.Thr1511Thr | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/53 | 4660/9368 | 4533/7377 | 1511/2458 | chr12 | 109237251 | ||
| chr12:109246238
|
T | C | 4 | a0001c0032a0001c0064a0009c0096others(1): Show | 5 | HG01884.hp1 HG02280.hp2 HG02896.hp1 others(2): Show |
synonymous_variant | LOW | c.5361T>C | p.Asp1787Asp | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/53 | 5488/9368 | 5361/7377 | 1787/2458 | chr12 | 109246238 | ||
| chr12:109253132
|
C | T | 1 | a0002c0086 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.6019C>T | p.Leu2007Leu | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 43/53 | 6146/9368 | 6019/7377 | 2007/2458 | chr12 | 109253132 | ||
| chr12:109254252
|
C | T | 1 | a0027c0065 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.6084C>T | p.Asp2028Asp | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/53 | 6211/9368 | 6084/7377 | 2028/2458 | chr12 | 109254252 | ||
| chr12:109256177
|
C | T | 27 | a0001c0002a0001c0011a0001c0013others(24): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
synonymous_variant | LOW | c.6204C>T | p.His2068His | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/53 | 6331/9368 | 6204/7377 | 2068/2458 | chr12 | 109256177 | ||
| chr12:109259023
|
C | T | 1 | a0001c0032 | 2 | HG02896.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.6411C>T | p.Thr2137Thr | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/53 | 6538/9368 | 6411/7377 | 2137/2458 | chr12 | 109259023 | ||
| chr12:109265133
|
A | G | 1 | a0006c0122 | 1 | HG02897.hp1 | synonymous_variant | LOW | c.6966A>G | p.Ala2322Ala | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 51/53 | 7093/9368 | 6966/7377 | 2322/2458 | chr12 | 109265133 | ||
| chr12:109265256
|
C | T | 1 | a0003c0081 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.7089C>T | p.Phe2363Phe | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 51/53 | 7216/9368 | 7089/7377 | 2363/2458 | chr12 | 109265256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109116601
|
G | A | 1 | a0001c0004t0017 | 1 | HG03130.hp1 | 5_prime_UTR_variant | MODIFIER | c.-113G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/53 | 22805 | chr12 | 109116601 | |||||
| chr12:109116690
|
G | A | 3 | a0001c0107t0012a0001c0124t0012a0034c0102t0018 | 3 | HG01891.hp2 HG03209.hp1 NA20300.hp2 |
5_prime_UTR_variant | MODIFIER | c.-24G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/53 | 22716 | chr12 | 109116690 | |||||
| chr12:109266372
|
G | A | 69 | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(66): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*10G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 10 | chr12 | 109266372 | |||||
| chr12:109266520
|
C | T | 116 | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(113): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*158C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 158 | chr12 | 109266520 | |||||
| chr12:109266692
|
G | A | 1 | a0002c0007t0022 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 330 | chr12 | 109266692 | |||||
| chr12:109266814
|
T | A | 4 | a0006c0031t0013a0011c0027t0013a0017c0123t0015others(1): Show | 4 | HG01168.hp2 HG01884.hp1 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*452T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 452 | chr12 | 109266814 | |||||
| chr12:109266905
|
A | AT | 41 | a0001c0003t0002a0001c0004t0002a0001c0004t0020others(38): Show | 85 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*560dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 561 | INFO_REALIGN_3_PRIME | chr12 | 109266905 | ||||
| chr12:109266905
|
A | ATT | 40 | a0001c0003t0004a0001c0004t0007a0001c0004t0017others(37): Show | 61 | HG00735.hp2 HG01123.hp1 HG01168.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*559_*560dupTT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 561 | INFO_REALIGN_3_PRIME | chr12 | 109266905 | ||||
| chr12:109266905
|
A | ATTT | 31 | a0001c0002t0001a0001c0002t0021a0001c0010t0001others(28): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*558_*560dupTTT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 561 | INFO_REALIGN_3_PRIME | chr12 | 109266905 | ||||
| chr12:109266905
|
A | ATTTT | 4 | a0001c0002t0008a0001c0011t0008a0003c0001t0008others(1): Show | 6 | HG02074.hp1 NA18970.hp1 NA18974.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*557_*560dupTTTT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 561 | INFO_REALIGN_3_PRIME | chr12 | 109266905 | ||||
| chr12:109267002
|
T | G | 1 | a0001c0062t0019 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*640T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 640 | chr12 | 109267002 | |||||
| chr12:109267008
|
A | G | 1 | a0001c0062t0019 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*646A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 646 | chr12 | 109267008 | |||||
| chr12:109267147
|
C | A | 8 | a0002c0006t0005a0002c0017t0024a0002c0053t0005others(5): Show | 14 | HG01081.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*785C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 785 | chr12 | 109267147 | |||||
| chr12:109267232
|
G | A | 1 | a0001c0002t0021 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*870G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 870 | chr12 | 109267232 | |||||
| chr12:109267363
|
T | C | 4 | a0001c0010t0009a0001c0016t0009a0001c0064t0009others(1): Show | 6 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1001T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 1001 | chr12 | 109267363 | |||||
| chr12:109267806
|
A | G | 122 | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(119): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*1444A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 1444 | chr12 | 109267806 | |||||
| chr12:109267952
|
AGACAAAA others(17): Show |
A | 2 | a0001c0004t0007a0001c0004t0020 | 8 | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1595_*1618delAAAT others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 1595 | INFO_REALIGN_3_PRIME | chr12 | 109267952 | ||||
| chr12:109267972
|
C | T | 1 | a0018c0051t0023 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1610C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 1610 | chr12 | 109267972 | |||||
| chr12:109268146
|
G | A | 6 | a0002c0007t0006a0002c0021t0006a0002c0036t0006others(3): Show | 9 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1784G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 1784 | chr12 | 109268146 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109116726
|
C | T | 41 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0002t0008g0306others(38): Show | 41 | HG01069.hp1 HG01074.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.-10+22C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109116726 | ||||||
| chr12:109116835
|
C | T | 35 | a0001c0002t0001g0235a0001c0002t0001g0241a0001c0002t0001g0242others(32): Show | 35 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.-10+131C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109116835 | ||||||
| chr12:109117047
|
C | CT | 75 | a0001c0002t0001g0191a0001c0003t0002g0193a0001c0010t0001g0188others(72): Show | 75 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.-10+366dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109117047 | |||||
| chr12:109117047
|
C | CTT | 70 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0002t0008g0306others(67): Show | 70 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.-10+365_-10+366dup others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109117047 | |||||
| chr12:109117166
|
C | T | 3 | a0001c0107t0012g0196a0001c0124t0012g0197a0034c0102t0018g0195 | 3 | HG01891.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-10+462C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109117166 | ||||||
| chr12:109117322
|
T | C | 3 | a0001c0045t0002g0234a0002c0020t0003g0232a0002c0020t0003g0233 | 3 | NA18952.hp1 NA18994.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-10+618T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109117322 | ||||||
| chr12:109117359
|
CA | C | 179 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0081others(176): Show | 179 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-10+670delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109117359 | |||||
| chr12:109117462
|
C | A | 191 | a0001c0002t0001g0235a0001c0002t0001g0241a0001c0002t0001g0242others(188): Show | 191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.-10+758C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109117462 | ||||||
| chr12:109117527
|
G | T | 1 | a0002c0006t0003g0194 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-10+823G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109117527 | ||||||
| chr12:109117565
|
A | G | 11 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0058t0016g0187others(8): Show | 11 | HG00323.hp1 HG01167.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10+861A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109117565 | ||||||
| chr12:109117719
|
C | A | 193 | a0001c0002t0001g0235a0001c0002t0001g0241a0001c0002t0001g0242others(190): Show | 193 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.-10+1015C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109117719 | ||||||
| chr12:109117847
|
C | T | 148 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0002t0008g0306others(145): Show | 148 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.-10+1143C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109117847 | ||||||
| chr12:109118238
|
C | T | 32 | a0001c0002t0001g0235a0001c0002t0001g0241a0001c0002t0001g0242others(29): Show | 32 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.-10+1534C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109118238 | ||||||
| chr12:109118412
|
C | CT | 8 | a0001c0002t0008g0306a0001c0004t0002g0054a0001c0011t0001g0056others(5): Show | 8 | HG01433.hp1 HG01884.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+1727dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109118412 | |||||
| chr12:109118412
|
CT | C | 78 | a0001c0003t0002g0068a0001c0010t0001g0188a0001c0010t0009g0186others(75): Show | 78 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.-10+1727delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109118412 | |||||
| chr12:109118468
|
C | T | 1 | a0001c0002t0001g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-10+1764C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109118468 | ||||||
| chr12:109118489
|
C | T | 1 | a0011c0027t0013g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-10+1785C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109118489 | ||||||
| chr12:109118524
|
C | T | 1 | a0005c0009t0006g0177 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-10+1820C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109118524 | ||||||
| chr12:109118713
|
C | T | 1 | a0005c0056t0003g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-10+2009C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109118713 | ||||||
| chr12:109118769
|
T | C | 1 | a0028c0100t0001g0070 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-10+2065T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109118769 | ||||||
| chr12:109118846
|
G | T | 7 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0058t0016g0187others(4): Show | 7 | HG01167.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+2142G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109118846 | ||||||
| chr12:109118904
|
A | G | 1 | a0002c0118t0005g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10+2200A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109118904 | ||||||
| chr12:109119205
|
A | G | 200 | a0001c0002t0001g0235a0001c0002t0001g0241a0001c0002t0001g0242others(197): Show | 200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-10+2501A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109119205 | ||||||
| chr12:109119266
|
C | T | 1 | a0004c0008t0001g0227 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-10+2562C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109119266 | ||||||
| chr12:109119378
|
T | C | 1 | a0038c0082t0002g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-10+2674T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109119378 | ||||||
| chr12:109119390
|
G | C | 1 | a0007c0104t0004g0183 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-10+2686G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109119390 | ||||||
| chr12:109119589
|
C | CA | 6 | a0001c0038t0001g0201a0002c0070t0005g0199a0003c0001t0008g0128others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+2901dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109119589 | |||||
| chr12:109119589
|
CA | C | 82 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0282others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-10+2901delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109119589 | |||||
| chr12:109119686
|
C | T | 3 | a0006c0026t0016g0066a0006c0078t0001g0181a0008c0044t0003g0182 | 3 | HG00323.hp1 NA18992.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-10+2982C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109119686 | ||||||
| chr12:109119810
|
G | A | 1 | a0015c0114t0004g0009 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-10+3106G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109119810 | ||||||
| chr12:109119849
|
C | T | 6 | a0001c0003t0002g0193a0001c0023t0001g0122a0001c0023t0004g0121others(3): Show | 6 | HG00735.hp2 HG01175.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+3145C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109119849 | ||||||
| chr12:109119984
|
G | A | 3 | a0006c0026t0016g0066a0006c0078t0001g0181a0008c0044t0003g0182 | 3 | HG00323.hp1 NA18992.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-10+3280G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109119984 | ||||||
| chr12:109120291
|
C | G | 3 | a0001c0010t0002g0261a0001c0012t0002g0262a0002c0086t0003g0260 | 3 | HG00423.hp1 HG02015.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.-10+3587C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109120291 | ||||||
| chr12:109120392
|
T | C | 43 | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0009g0186others(40): Show | 43 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.-10+3688T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109120392 | ||||||
| chr12:109120395
|
G | A | 1 | a0036c0094t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-10+3691G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109120395 | ||||||
| chr12:109120507
|
G | A | 1 | a0002c0020t0003g0273 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-10+3803G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109120507 | ||||||
| chr12:109120524
|
G | A | 1 | a0001c0054t0001g0203 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-10+3820G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109120524 | ||||||
| chr12:109120601
|
C | T | 1 | a0002c0118t0005g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10+3897C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109120601 | ||||||
| chr12:109120756
|
G | A | 2 | a0007c0037t0004g0073a0039c0080t0010g0071 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-10+4052G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109120756 | ||||||
| chr12:109120785
|
C | T | 41 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0002t0008g0306others(38): Show | 41 | HG01069.hp1 HG01074.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.-10+4081C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109120785 | ||||||
| chr12:109120833
|
T | C | 85 | a0001c0002t0001g0075a0001c0002t0001g0241a0001c0002t0001g0242others(82): Show | 85 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-10+4129T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109120833 | ||||||
| chr12:109121259
|
A | G | 1 | a0001c0054t0001g0203 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-10+4555A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109121259 | ||||||
| chr12:109121359
|
G | A | 2 | a0001c0074t0004g0229a0017c0123t0015g0058 | 2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-10+4655G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109121359 | ||||||
| chr12:109121521
|
A | G | 282 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(279): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.-10+4817A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109121521 | ||||||
| chr12:109121525
|
G | A | 8 | a0001c0038t0001g0201a0001c0069t0002g0204a0002c0070t0005g0199others(5): Show | 8 | HG02145.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+4821G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109121525 | ||||||
| chr12:109121674
|
A | G | 83 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0282others(80): Show | 83 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.-10+4970A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109121674 | ||||||
| chr12:109121774
|
G | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-10+5070G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109121774 | ||||||
| chr12:109121974
|
G | A | 7 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0109t0002g0276others(4): Show | 7 | HG01074.hp1 HG01175.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+5270G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109121974 | ||||||
| chr12:109122040
|
C | T | 4 | a0001c0069t0002g0204a0006c0031t0004g0002a0006c0031t0004g0206others(1): Show | 4 | HG02809.hp1 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+5336C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109122040 | ||||||
| chr12:109122204
|
G | T | 12 | a0001c0002t0008g0306a0001c0003t0004g0300a0002c0014t0003g0303others(9): Show | 12 | HG01069.hp1 HG01106.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10+5500G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109122204 | ||||||
| chr12:109122302
|
G | T | 1 | a0004c0008t0001g0198 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-10+5598G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109122302 | ||||||
| chr12:109122334
|
G | C | 3 | a0001c0107t0012g0196a0001c0124t0012g0197a0034c0102t0018g0195 | 3 | HG01891.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-10+5630G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109122334 | ||||||
| chr12:109122376
|
C | T | 2 | a0002c0020t0003g0120a0004c0112t0001g0119 | 2 | HG02074.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-10+5672C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109122376 | ||||||
| chr12:109122408
|
T | C | 15 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0016t0009g0287others(12): Show | 15 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10+5704T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109122408 | ||||||
| chr12:109122423
|
G | A | 35 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(32): Show | 35 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.-10+5719G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109122423 | ||||||
| chr12:109122491
|
T | C | 1 | a0005c0019t0006g0076 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-10+5787T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109122491 | ||||||
| chr12:109122530
|
G | A | 2 | a0007c0037t0004g0073a0039c0080t0010g0071 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-10+5826G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109122530 | ||||||
| chr12:109122572
|
C | CA | 56 | a0001c0002t0001g0079a0001c0002t0001g0081a0001c0002t0001g0282others(53): Show | 56 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.-10+5893dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109122572 | |||||
| chr12:109122572
|
C | CAA | 39 | a0001c0002t0008g0306a0001c0003t0004g0300a0001c0004t0017g0003others(36): Show | 39 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-10+5892_-10+5893d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109122572 | |||||
| chr12:109122572
|
CA | C | 72 | a0001c0011t0001g0157a0001c0012t0002g0045a0001c0012t0002g0259others(69): Show | 72 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-10+5893delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109122572 | |||||
| chr12:109122780
|
G | A | 2 | a0001c0074t0004g0229a0017c0123t0015g0058 | 2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-10+6076G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109122780 | ||||||
| chr12:109122827
|
G | A | 2 | a0001c0074t0004g0229a0017c0123t0015g0058 | 2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-10+6123G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109122827 | ||||||
| chr12:109122898
|
T | G | 1 | a0001c0002t0008g0306 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-10+6194T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109122898 | ||||||
| chr12:109123009
|
G | A | 32 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(29): Show | 32 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.-10+6305G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123009 | ||||||
| chr12:109123035
|
G | T | 32 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(29): Show | 32 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.-10+6331G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123035 | ||||||
| chr12:109123180
|
C | CA | 81 | a0001c0002t0001g0085a0001c0002t0001g0241a0001c0002t0001g0242others(78): Show | 81 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.-10+6492dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109123180 | |||||
| chr12:109123195
|
A | T | 1 | a0002c0117t0003g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-10+6491A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123195 | ||||||
| chr12:109123196
|
A | T | 1 | a0002c0117t0003g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-10+6492A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123196 | ||||||
| chr12:109123212
|
G | A | 1 | a0017c0123t0015g0058 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+6508G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123212 | ||||||
| chr12:109123231
|
G | A | 44 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0002t0008g0306others(41): Show | 44 | HG01069.hp1 HG01074.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.-10+6527G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123231 | ||||||
| chr12:109123339
|
G | A | 44 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0002t0008g0306others(41): Show | 44 | HG01069.hp1 HG01074.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.-10+6635G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123339 | ||||||
| chr12:109123415
|
A | G | 44 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0002t0008g0306others(41): Show | 44 | HG01069.hp1 HG01074.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.-10+6711A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123415 | ||||||
| chr12:109123458
|
G | A | 4 | a0002c0118t0005g0231a0006c0026t0016g0066a0006c0078t0001g0181others(1): Show | 4 | HG00323.hp1 HG02258.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+6754G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123458 | ||||||
| chr12:109123511
|
G | A | 1 | a0038c0082t0002g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-10+6807G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123511 | ||||||
| chr12:109123518
|
G | T | 149 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(146): Show | 149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.-10+6814G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123518 | ||||||
| chr12:109123552
|
G | C | 1 | a0001c0048t0002g0281 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-10+6848G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123552 | ||||||
| chr12:109123575
|
C | T | 1 | a0001c0124t0012g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-10+6871C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123575 | ||||||
| chr12:109123635
|
T | C | 160 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0002t0008g0306others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.-10+6931T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123635 | ||||||
| chr12:109123676
|
G | A | 1 | a0003c0005t0002g0131 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-10+6972G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123676 | ||||||
| chr12:109123726
|
C | T | 164 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0002t0008g0306others(161): Show | 164 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.-10+7022C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123726 | ||||||
| chr12:109123757
|
G | A | 159 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0002t0008g0306others(156): Show | 159 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.-10+7053G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123757 | ||||||
| chr12:109123763
|
CT | C | 306 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-10+7061delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109123763 | |||||
| chr12:109123858
|
A | T | 4 | a0002c0007t0003g0041a0002c0017t0003g0042a0006c0120t0003g0043others(1): Show | 4 | HG01109.hp2 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+7154A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123858 | ||||||
| chr12:109123877
|
A | G | 2 | a0001c0002t0001g0114a0023c0099t0001g0084 | 2 | NA18950.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.-10+7173A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123877 | ||||||
| chr12:109123897
|
C | G | 3 | a0001c0107t0012g0196a0001c0124t0012g0197a0034c0102t0018g0195 | 3 | HG01891.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-10+7193C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123897 | ||||||
| chr12:109123898
|
G | A | 4 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(1): Show | 4 | HG03139.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+7194G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109123898 | ||||||
| chr12:109124075
|
G | GT | 33 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(30): Show | 33 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.-10+7381dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109124075 | |||||
| chr12:109124086
|
A | T | 1 | a0008c0044t0003g0182 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-10+7382A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109124086 | ||||||
| chr12:109124350
|
AGTGTCAT others(23): Show |
A | 1 | a0001c0003t0002g0077 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-10+7647_-10+7676d others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109124350 | ||||||
| chr12:109124363
|
A | G | 3 | a0001c0107t0012g0196a0001c0124t0012g0197a0034c0102t0018g0195 | 3 | HG01891.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-10+7659A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109124363 | ||||||
| chr12:109124430
|
A | G | 199 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0282others(196): Show | 199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.-10+7726A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109124430 | ||||||
| chr12:109124475
|
G | T | 193 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0282others(190): Show | 193 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.-10+7771G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109124475 | ||||||
| chr12:109124554
|
G | A | 24 | a0001c0004t0017g0003a0001c0034t0001g0211a0001c0034t0001g0212others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.-10+7850G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109124554 | ||||||
| chr12:109124655
|
G | A | 119 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0282others(116): Show | 119 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-10+7951G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109124655 | ||||||
| chr12:109124690
|
T | G | 4 | a0002c0118t0005g0231a0006c0026t0016g0066a0006c0078t0001g0181others(1): Show | 4 | HG00323.hp1 HG02258.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+7986T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109124690 | ||||||
| chr12:109124709
|
T | A | 35 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(32): Show | 35 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.-10+8005T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109124709 | ||||||
| chr12:109124788
|
C | T | 3 | a0001c0107t0012g0196a0001c0124t0012g0197a0034c0102t0018g0195 | 3 | HG01891.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-10+8084C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109124788 | ||||||
| chr12:109124895
|
T | G | 41 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0002t0008g0306others(38): Show | 41 | HG01069.hp1 HG01074.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.-10+8191T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109124895 | ||||||
| chr12:109124917
|
C | T | 1 | a0014c0079t0004g0180 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-10+8213C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109124917 | ||||||
| chr12:109124918
|
A | G | 124 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(121): Show | 124 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-10+8214A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109124918 | ||||||
| chr12:109125010
|
G | A | 31 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(28): Show | 31 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.-10+8306G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109125010 | ||||||
| chr12:109125115
|
T | G | 5 | a0002c0014t0003g0303a0002c0024t0003g0302a0009c0025t0001g0269others(2): Show | 5 | HG01069.hp1 HG01106.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+8411T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109125115 | ||||||
| chr12:109125333
|
T | C | 4 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(1): Show | 4 | HG03139.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+8629T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109125333 | ||||||
| chr12:109125376
|
A | C | 199 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0282others(196): Show | 199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.-10+8672A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109125376 | ||||||
| chr12:109125451
|
G | A | 1 | a0002c0118t0005g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10+8747G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109125451 | ||||||
| chr12:109125524
|
G | C | 7 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0058t0016g0187others(4): Show | 7 | HG01167.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+8820G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109125524 | ||||||
| chr12:109125833
|
T | C | 1 | a0007c0057t0004g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-10+9129T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109125833 | ||||||
| chr12:109126030
|
C | T | 5 | a0001c0039t0004g0116a0002c0092t0010g0192a0014c0077t0004g0118others(2): Show | 5 | HG02257.hp1 HG02559.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+9326C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109126030 | ||||||
| chr12:109126130
|
C | G | 39 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.-10+9426C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109126130 | ||||||
| chr12:109126295
|
G | A | 39 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.-10+9591G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109126295 | ||||||
| chr12:109126303
|
G | A | 39 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.-10+9599G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109126303 | ||||||
| chr12:109126422
|
C | A | 2 | a0007c0037t0004g0073a0039c0080t0010g0071 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-10+9718C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109126422 | ||||||
| chr12:109126508
|
C | A | 1 | a0014c0079t0004g0180 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-10+9804C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109126508 | ||||||
| chr12:109126548
|
G | A | 2 | a0001c0055t0001g0226a0027c0065t0005g0225 | 2 | HG01081.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-10+9844G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109126548 | ||||||
| chr12:109126708
|
T | TAAAA | 39 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.-10+10006_-10+1000 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109126708 | |||||
| chr12:109126944
|
C | A | 1 | a0001c0003t0002g0077 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-10+10240C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109126944 | ||||||
| chr12:109126945
|
C | A | 1 | a0001c0003t0002g0077 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-10+10241C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109126945 | ||||||
| chr12:109126946
|
C | CATAAATT others(10): Show |
1 | a0001c0003t0002g0077 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-10+10242_-10+1024 others(21): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109126946 | ||||||
| chr12:109126947
|
G | C | 1 | a0001c0003t0002g0077 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-10+10243G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109126947 | ||||||
| chr12:109126948
|
T | TACTCA | 197 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0282others(194): Show | 197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.-10+10248_-10+1024 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109126948 | |||||
| chr12:109126966
|
T | C | 32 | a0001c0004t0017g0003a0001c0034t0001g0211a0001c0034t0001g0212others(29): Show | 32 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.-10+10262T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109126966 | ||||||
| chr12:109126979
|
A | G | 2 | a0016c0047t0002g0175a0016c0047t0002g0176 | 2 | NA18974.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-10+10275A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109126979 | ||||||
| chr12:109127110
|
C | T | 39 | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0009g0186others(36): Show | 39 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-10+10406C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109127110 | ||||||
| chr12:109127157
|
C | T | 2 | a0001c0032t0004g0291a0001c0032t0004g0292 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-10+10453C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109127157 | ||||||
| chr12:109127173
|
G | A | 1 | a0002c0117t0003g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-10+10469G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109127173 | ||||||
| chr12:109127288
|
G | A | 1 | a0027c0065t0005g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-10+10584G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109127288 | ||||||
| chr12:109127421
|
G | GA | 109 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0300others(106): Show | 109 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.-10+10729dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109127421 | |||||
| chr12:109127436
|
C | A | 1 | a0001c0003t0002g0077 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-10+10732C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109127436 | ||||||
| chr12:109127443
|
C | A | 1 | a0002c0118t0005g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10+10739C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109127443 | ||||||
| chr12:109127489
|
C | G | 32 | a0001c0004t0017g0003a0001c0034t0001g0211a0001c0034t0001g0212others(29): Show | 32 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.-10+10785C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109127489 | ||||||
| chr12:109127597
|
T | TA | 39 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.-10+10906dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109127597 | |||||
| chr12:109127605
|
A | G | 1 | a0001c0003t0004g0300 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-10+10901A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109127605 | ||||||
| chr12:109127710
|
A | G | 1 | a0036c0094t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-10+11006A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109127710 | ||||||
| chr12:109127801
|
T | A | 1 | a0002c0021t0006g0239 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-10+11097T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109127801 | ||||||
| chr12:109127825
|
C | G | 39 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.-10+11121C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109127825 | ||||||
| chr12:109128097
|
C | T | 43 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0002t0008g0306others(40): Show | 43 | HG00597.hp1 HG01069.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.-9-11300C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109128097 | ||||||
| chr12:109128134
|
C | T | 1 | a0024c0091t0002g0174 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-9-11263C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109128134 | ||||||
| chr12:109128141
|
T | C | 1 | a0014c0079t0004g0180 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-9-11256T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109128141 | ||||||
| chr12:109128145
|
T | G | 32 | a0001c0004t0017g0003a0001c0034t0001g0211a0001c0034t0001g0212others(29): Show | 32 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.-9-11252T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109128145 | ||||||
| chr12:109128288
|
A | C | 1 | a0001c0060t0002g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-9-11109A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109128288 | ||||||
| chr12:109128326
|
C | CT | 31 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(28): Show | 31 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.-9-11064dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109128326 | |||||
| chr12:109128329
|
TTTTTATT others(3): Show |
T | 7 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0058t0016g0187others(4): Show | 7 | HG01167.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-11053_-9-11044d others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109128329 | |||||
| chr12:109128333
|
T | A | 1 | a0014c0079t0004g0180 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-9-11064T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109128333 | ||||||
| chr12:109128338
|
T | A | 1 | a0014c0079t0004g0180 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-9-11059T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109128338 | ||||||
| chr12:109128344
|
A | G | 1 | a0001c0060t0002g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-9-11053A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109128344 | ||||||
| chr12:109128359
|
C | T | 67 | a0001c0011t0001g0157a0001c0013t0001g0153a0001c0013t0001g0163others(64): Show | 67 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.-9-11038C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109128359 | ||||||
| chr12:109128647
|
G | T | 4 | a0002c0007t0003g0041a0002c0017t0003g0042a0006c0120t0003g0043others(1): Show | 4 | HG01109.hp2 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-10750G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109128647 | ||||||
| chr12:109128752
|
CT | C | 42 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(39): Show | 42 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.-9-10631delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109128752 | |||||
| chr12:109128835
|
G | A | 1 | a0001c0095t0001g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-9-10562G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109128835 | ||||||
| chr12:109128838
|
A | G | 41 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0002t0008g0306others(38): Show | 41 | HG01069.hp1 HG01074.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.-9-10559A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109128838 | ||||||
| chr12:109128898
|
G | A | 306 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-9-10499G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109128898 | ||||||
| chr12:109129104
|
AAAAT | A | 76 | a0001c0011t0001g0157a0001c0013t0001g0153a0001c0013t0001g0163others(73): Show | 76 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.-9-10277_-9-10274d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109129104 | |||||
| chr12:109129124
|
A | T | 2 | a0001c0003t0002g0112a0002c0014t0003g0113 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-9-10273A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109129124 | ||||||
| chr12:109129264
|
C | T | 3 | a0001c0107t0012g0196a0001c0124t0012g0197a0034c0102t0018g0195 | 3 | HG01891.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-9-10133C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109129264 | ||||||
| chr12:109129334
|
G | C | 1 | a0014c0079t0004g0180 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-9-10063G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109129334 | ||||||
| chr12:109129430
|
G | A | 39 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.-9-9967G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109129430 | ||||||
| chr12:109129430
|
G | T | 1 | a0001c0106t0001g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-9-9967G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109129430 | ||||||
| chr12:109129540
|
T | C | 39 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.-9-9857T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109129540 | ||||||
| chr12:109129605
|
A | G | 39 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.-9-9792A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109129605 | ||||||
| chr12:109129624
|
A | C | 1 | a0001c0048t0002g0281 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-9-9773A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109129624 | ||||||
| chr12:109129788
|
C | T | 1 | a0001c0054t0001g0203 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-9-9609C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109129788 | ||||||
| chr12:109129854
|
C | T | 4 | a0001c0039t0004g0116a0002c0092t0010g0192a0014c0079t0004g0180others(1): Show | 4 | HG01433.hp1 HG02257.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-9543C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109129854 | ||||||
| chr12:109129898
|
CA | C | 35 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(32): Show | 35 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.-9-9498delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109129898 | ||||||
| chr12:109129903
|
C | T | 2 | a0002c0014t0003g0083a0012c0035t0004g0082 | 2 | HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-9-9494C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109129903 | ||||||
| chr12:109130110
|
C | T | 1 | a0001c0016t0009g0290 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-9-9287C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109130110 | ||||||
| chr12:109130301
|
G | A | 1 | a0001c0087t0001g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-9-9096G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109130301 | ||||||
| chr12:109130349
|
G | C | 35 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(32): Show | 35 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.-9-9048G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109130349 | ||||||
| chr12:109130414
|
G | A | 2 | a0002c0007t0022g0032a0002c0053t0005g0033 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-9-8983G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109130414 | ||||||
| chr12:109130476
|
G | A | 71 | a0001c0011t0001g0157a0001c0013t0001g0153a0001c0013t0001g0163others(68): Show | 71 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-9-8921G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109130476 | ||||||
| chr12:109130704
|
C | T | 2 | a0001c0055t0001g0226a0027c0065t0005g0225 | 2 | HG01081.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-9-8693C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109130704 | ||||||
| chr12:109130773
|
G | A | 2 | a0001c0074t0004g0229a0017c0123t0015g0058 | 2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-9-8624G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109130773 | ||||||
| chr12:109130861
|
T | C | 1 | a0026c0066t0015g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-9-8536T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109130861 | ||||||
| chr12:109130992
|
T | C | 106 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(103): Show | 106 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-9-8405T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109130992 | ||||||
| chr12:109131230
|
T | C | 1 | a0001c0011t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-9-8167T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109131230 | ||||||
| chr12:109131263
|
A | G | 52 | a0001c0003t0004g0300a0001c0004t0017g0003a0001c0010t0001g0188others(49): Show | 52 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-9-8134A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109131263 | ||||||
| chr12:109131311
|
C | T | 1 | a0001c0038t0001g0029 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-9-8086C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109131311 | ||||||
| chr12:109131425
|
C | T | 1 | a0005c0009t0003g0164 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-9-7972C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109131425 | ||||||
| chr12:109131589
|
C | T | 77 | a0001c0010t0002g0261a0001c0012t0002g0045a0001c0012t0002g0250others(74): Show | 77 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.-9-7808C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109131589 | ||||||
| chr12:109131852
|
T | C | 64 | a0001c0013t0001g0153a0001c0016t0011g0274a0001c0045t0002g0146others(61): Show | 64 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.-9-7545T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109131852 | ||||||
| chr12:109131886
|
T | C | 1 | a0026c0066t0015g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-9-7511T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109131886 | ||||||
| chr12:109131908
|
G | A | 1 | a0002c0088t0006g0247 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-9-7489G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109131908 | ||||||
| chr12:109132129
|
C | T | 5 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(2): Show | 5 | HG00323.hp1 HG02523.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-7268C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109132129 | ||||||
| chr12:109132141
|
A | G | 124 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(121): Show | 124 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-9-7256A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109132141 | ||||||
| chr12:109132145
|
C | T | 47 | a0001c0013t0001g0153a0001c0045t0002g0146a0002c0061t0003g0062others(44): Show | 47 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9-7252C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109132145 | ||||||
| chr12:109132171
|
C | CT | 77 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(74): Show | 77 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.-9-7215dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109132171 | |||||
| chr12:109132243
|
C | A | 6 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(3): Show | 6 | HG01433.hp1 HG02280.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-7154C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109132243 | ||||||
| chr12:109132271
|
T | C | 1 | a0003c0001t0001g0158 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-9-7126T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109132271 | ||||||
| chr12:109132310
|
G | A | 1 | a0001c0111t0001g0275 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-9-7087G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109132310 | ||||||
| chr12:109132542
|
G | A | 4 | a0002c0007t0003g0041a0002c0007t0022g0032a0002c0017t0003g0042others(1): Show | 4 | HG02615.hp1 HG03195.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-6855G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109132542 | ||||||
| chr12:109132690
|
G | A | 10 | a0001c0002t0001g0282a0001c0002t0008g0306a0001c0003t0004g0300others(7): Show | 10 | HG01069.hp1 HG01106.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-6707G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109132690 | ||||||
| chr12:109132814
|
G | C | 1 | a0001c0048t0002g0281 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-9-6583G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109132814 | ||||||
| chr12:109132863
|
G | T | 5 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0039t0004g0116others(2): Show | 5 | HG01167.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-6534G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109132863 | ||||||
| chr12:109132925
|
G | A | 1 | a0001c0011t0001g0008 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-9-6472G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109132925 | ||||||
| chr12:109132960
|
A | G | 1 | a0001c0048t0002g0281 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-9-6437A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109132960 | ||||||
| chr12:109132974
|
G | A | 6 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(3): Show | 6 | HG00323.hp1 HG02523.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-6423G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109132974 | ||||||
| chr12:109133016
|
C | G | 1 | a0002c0020t0003g0120 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-9-6381C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133016 | ||||||
| chr12:109133240
|
T | TTC | 4 | a0001c0002t0001g0075a0001c0003t0004g0074a0001c0049t0001g0289others(1): Show | 4 | HG02257.hp2 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-6132_-9-6131dup others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133240 | |||||
| chr12:109133240
|
TTC | T | 14 | a0001c0004t0017g0003a0001c0038t0001g0201a0002c0070t0005g0199others(11): Show | 14 | HG00408.hp1 HG01081.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9-6132_-9-6131del others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133240 | |||||
| chr12:109133240
|
TTCTC | T | 128 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(125): Show | 128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-9-6134_-9-6131del others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133240 | |||||
| chr12:109133240
|
TTCTCTC | T | 3 | a0001c0016t0011g0274a0001c0069t0002g0204a0002c0092t0010g0192 | 3 | HG02965.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-9-6136_-9-6131del others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133240 | |||||
| chr12:109133836
|
C | CAT | 13 | a0001c0002t0001g0191a0001c0048t0004g0307a0001c0050t0001g0278others(10): Show | 13 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9-5534_-9-5533dup others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133836 | |||||
| chr12:109133836
|
C | CATAT | 15 | a0001c0002t0001g0079a0001c0002t0001g0085a0001c0003t0002g0101others(12): Show | 15 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-5536_-9-5533dup others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133836 | |||||
| chr12:109133836
|
C | CATATAT | 8 | a0001c0002t0001g0035a0001c0003t0002g0094a0001c0003t0002g0244others(5): Show | 8 | HG02080.hp1 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-5538_-9-5533dup others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133836 | |||||
| chr12:109133836
|
C | CATATATA others(1): Show |
10 | a0001c0002t0001g0091a0001c0002t0001g0283a0001c0003t0002g0078others(7): Show | 10 | HG01070.hp1 HG01258.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9-5540_-9-5533dup others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133836 | |||||
| chr12:109133836
|
C | CATATATA others(3): Show |
7 | a0001c0022t0004g0006a0002c0006t0005g0284a0006c0121t0004g0170others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-5542_-9-5533dup others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133836 | |||||
| chr12:109133836
|
C | CATATATA others(5): Show |
4 | a0006c0031t0004g0206a0008c0015t0005g0057a0008c0015t0005g0171others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-5544_-9-5533dup others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133836 | |||||
| chr12:109133836
|
C | CATATATA others(7): Show |
4 | a0002c0118t0005g0231a0006c0026t0002g0155a0006c0031t0004g0002others(1): Show | 4 | HG01109.hp2 HG02258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-5546_-9-5533dup others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133836 | |||||
| chr12:109133836
|
C | CATATATA others(9): Show |
2 | a0013c0033t0002g0185a0013c0033t0002g0189 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-9-5548_-9-5533dup others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133836 | |||||
| chr12:109133851
|
A | C | 117 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-9-5546A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133851 | ||||||
| chr12:109133859
|
ATATATTT others(6): Show |
A | 1 | a0014c0077t0004g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-9-5536_-9-5524del others(13): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133859 | |||||
| chr12:109133861
|
ATATTTTT others(5): Show |
A | 12 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0013t0001g0153others(9): Show | 12 | HG00544.hp1 HG00558.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9-5534_-9-5523del others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133861 | |||||
| chr12:109133863
|
A | ATATATAT others(4): Show |
1 | a0001c0022t0004g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-9-5533_-9-5532ins others(11): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133863 | |||||
| chr12:109133863
|
A | ATATATAT others(4): Show |
1 | a0006c0078t0001g0181 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-9-5533_-9-5532ins others(11): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133863 | |||||
| chr12:109133863
|
A | ATATTTTT others(4): Show |
1 | a0027c0065t0005g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-9-5533_-9-5532ins others(11): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133863 | |||||
| chr12:109133863
|
A | T | 2 | a0007c0037t0004g0073a0007c0057t0004g0207 | 2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-9-5534A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133863 | ||||||
| chr12:109133863
|
AT | A | 12 | a0001c0002t0008g0306a0001c0003t0004g0300a0001c0004t0002g0054others(9): Show | 12 | HG01884.hp2 HG01943.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9-5515delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133863 | |||||
| chr12:109133863
|
ATTT | A | 6 | a0001c0016t0009g0287a0001c0016t0009g0290a0001c0016t0009g0305others(3): Show | 6 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-5517_-9-5515del others(3): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133863 | |||||
| chr12:109133863
|
ATTTTTTT others(5): Show |
A | 105 | a0001c0010t0002g0261a0001c0012t0002g0045a0001c0012t0002g0250others(102): Show | 105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-9-5526_-9-5515del others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133863 | |||||
| chr12:109133864
|
T | TA | 22 | a0001c0004t0002g0050a0001c0004t0002g0052a0001c0004t0007g0001others(19): Show | 23 | HG00597.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-9-5533_-9-5532ins others(1): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133864 | ||||||
| chr12:109133864
|
T | TATA | 8 | a0001c0002t0001g0081a0001c0002t0001g0098a0001c0003t0002g0097others(5): Show | 8 | HG00423.hp2 HG00438.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-5533_-9-5532ins others(3): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133864 | ||||||
| chr12:109133864
|
T | TATATA | 13 | a0001c0002t0001g0114a0001c0002t0001g0235a0001c0002t0001g0241others(10): Show | 13 | HG02027.hp2 HG02922.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-5533_-9-5532ins others(5): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133864 | ||||||
| chr12:109133864
|
T | TATATATA | 4 | a0001c0002t0001g0126a0001c0003t0002g0068a0002c0006t0005g0123others(1): Show | 4 | HG02074.hp2 HG02258.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-5533_-9-5532ins others(7): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133864 | ||||||
| chr12:109133864
|
T | TATATATA others(2): Show |
5 | a0001c0022t0004g0004a0001c0022t0004g0005a0002c0024t0003g0034others(2): Show | 5 | HG00323.hp1 HG03453.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-5533_-9-5532ins others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133864 | ||||||
| chr12:109133864
|
T | TATATATA others(4): Show |
8 | a0001c0023t0001g0122a0001c0038t0001g0201a0001c0046t0002g0190others(5): Show | 8 | HG01433.hp1 HG01891.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-5533_-9-5532ins others(11): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133864 | ||||||
| chr12:109133864
|
T | TATATATA others(6): Show |
2 | a0001c0023t0004g0121a0007c0037t0004g0200 | 2 | HG00735.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-9-5533_-9-5532ins others(13): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133864 | ||||||
| chr12:109133864
|
T | TATATATA others(8): Show |
1 | a0001c0023t0001g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-9-5533_-9-5532ins others(15): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133864 | ||||||
| chr12:109133864
|
T | TATATATA others(10): Show |
1 | a0002c0070t0005g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-9-5533_-9-5532ins others(17): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133864 | ||||||
| chr12:109133864
|
T | TATATATA others(14): Show |
1 | a0001c0124t0012g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-9-5533_-9-5532ins others(21): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133864 | ||||||
| chr12:109133865
|
T | A | 56 | a0001c0002t0001g0035a0001c0002t0001g0079a0001c0002t0001g0085others(53): Show | 56 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-9-5532T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133865 | ||||||
| chr12:109133866
|
T | A | 57 | a0001c0002t0001g0126a0001c0002t0001g0235a0001c0002t0001g0241others(54): Show | 58 | HG00423.hp2 HG00597.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.-9-5531T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133866 | ||||||
| chr12:109133867
|
T | A | 46 | a0001c0002t0001g0079a0001c0002t0001g0085a0001c0002t0001g0091others(43): Show | 46 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.-9-5530T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133867 | ||||||
| chr12:109133868
|
T | A | 20 | a0001c0002t0008g0306a0001c0003t0002g0068a0001c0003t0004g0074others(17): Show | 20 | HG00735.hp2 HG01070.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-9-5529T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133868 | ||||||
| chr12:109133869
|
T | A | 26 | a0001c0002t0001g0283a0001c0049t0001g0289a0001c0098t0001g0286others(23): Show | 26 | HG00642.hp1 HG01109.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.-9-5528T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133869 | ||||||
| chr12:109133870
|
T | A | 2 | a0002c0024t0003g0034a0006c0031t0013g0205 | 2 | HG03453.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-9-5527T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133870 | ||||||
| chr12:109133871
|
T | A | 9 | a0001c0002t0001g0283a0001c0105t0004g0296a0002c0006t0005g0294others(6): Show | 9 | HG01891.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9-5526T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133871 | ||||||
| chr12:109133873
|
T | A | 2 | a0001c0105t0004g0296a0002c0117t0003g0125 | 2 | HG02698.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-9-5524T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133873 | ||||||
| chr12:109133901
|
G | GT | 14 | a0001c0004t0017g0003a0001c0016t0011g0274a0001c0038t0001g0201others(11): Show | 14 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9-5484dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133901 | |||||
| chr12:109133901
|
GT | G | 68 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(65): Show | 68 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.-9-5484delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109133901 | |||||
| chr12:109133989
|
G | T | 4 | a0001c0002t0001g0235a0001c0002t0001g0241a0001c0002t0001g0242others(1): Show | 4 | HG02027.hp2 NA18950.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-5408G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109133989 | ||||||
| chr12:109134031
|
G | A | 1 | a0001c0039t0004g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-9-5366G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109134031 | ||||||
| chr12:109134173
|
C | G | 117 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-9-5224C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109134173 | ||||||
| chr12:109134323
|
T | C | 5 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0039t0004g0116others(2): Show | 5 | HG01167.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-5074T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109134323 | ||||||
| chr12:109134619
|
T | C | 2 | a0003c0001t0001g0087a0005c0019t0006g0076 | 2 | NA19060.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-9-4778T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109134619 | ||||||
| chr12:109135171
|
A | T | 2 | a0001c0049t0001g0289a0002c0006t0005g0284 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-9-4226A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109135171 | ||||||
| chr12:109135324
|
T | A | 121 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(118): Show | 121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-9-4073T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109135324 | ||||||
| chr12:109135342
|
G | A | 243 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-9-4055G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109135342 | ||||||
| chr12:109135398
|
T | A | 128 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(125): Show | 128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-9-3999T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109135398 | ||||||
| chr12:109135526
|
A | T | 3 | a0004c0008t0001g0221a0004c0041t0002g0222a0010c0042t0003g0220 | 3 | HG00642.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-9-3871A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109135526 | ||||||
| chr12:109135662
|
G | T | 3 | a0004c0008t0001g0221a0004c0041t0002g0222a0010c0042t0003g0220 | 3 | HG00642.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-9-3735G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109135662 | ||||||
| chr12:109135808
|
C | CT | 10 | a0001c0016t0009g0287a0001c0016t0009g0305a0001c0032t0004g0291others(7): Show | 10 | HG01433.hp1 HG01884.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9-3570dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109135808 | |||||
| chr12:109135808
|
C | CTT | 118 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(115): Show | 118 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-9-3571_-9-3570dup others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109135808 | |||||
| chr12:109135808
|
CT | C | 90 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(87): Show | 90 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.-9-3570delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109135808 | |||||
| chr12:109135902
|
C | T | 3 | a0001c0004t0002g0054a0001c0011t0001g0056a0002c0007t0003g0055 | 3 | HG01884.hp2 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-9-3495C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109135902 | ||||||
| chr12:109136373
|
A | G | 1 | a0001c0124t0012g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-9-3024A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109136373 | ||||||
| chr12:109136557
|
A | G | 1 | a0001c0002t0001g0283 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9-2840A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109136557 | ||||||
| chr12:109136580
|
G | T | 13 | a0002c0118t0005g0231a0006c0031t0004g0002a0006c0031t0004g0206others(10): Show | 13 | HG01109.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9-2817G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109136580 | ||||||
| chr12:109136631
|
T | A | 1 | a0001c0003t0002g0244 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-9-2766T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109136631 | ||||||
| chr12:109136961
|
G | A | 6 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(3): Show | 6 | HG00323.hp1 HG02523.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-2436G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109136961 | ||||||
| chr12:109137151
|
C | T | 69 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(66): Show | 69 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.-9-2246C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109137151 | ||||||
| chr12:109137257
|
GCAAATT | G | 35 | a0001c0010t0002g0261a0001c0012t0002g0045a0001c0012t0002g0250others(32): Show | 35 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.-9-2138_-9-2133del others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109137257 | |||||
| chr12:109137386
|
A | G | 242 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-9-2011A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109137386 | ||||||
| chr12:109137402
|
G | C | 1 | a0001c0124t0012g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-9-1995G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109137402 | ||||||
| chr12:109137416
|
T | C | 1 | a0014c0077t0004g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-9-1981T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109137416 | ||||||
| chr12:109137585
|
A | C | 1 | a0001c0029t0002g0096 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-9-1812A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109137585 | ||||||
| chr12:109137659
|
CA | C | 10 | a0001c0004t0007g0001a0001c0004t0007g0011a0001c0004t0007g0019others(7): Show | 11 | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-1725delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109137659 | |||||
| chr12:109137672
|
A | G | 6 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(3): Show | 6 | HG00323.hp1 HG02523.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-1725A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109137672 | ||||||
| chr12:109137791
|
T | A | 1 | a0002c0117t0003g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-9-1606T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109137791 | ||||||
| chr12:109137794
|
A | C | 7 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(4): Show | 7 | HG00323.hp1 HG02523.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-1603A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109137794 | ||||||
| chr12:109137899
|
C | CT | 89 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0013t0001g0153others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.-9-1487dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109137899 | |||||
| chr12:109137899
|
C | CTT | 53 | a0001c0010t0002g0261a0001c0012t0002g0045a0001c0012t0002g0250others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.-9-1488_-9-1487dup others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109137899 | |||||
| chr12:109138022
|
C | T | 6 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(3): Show | 6 | HG00323.hp1 HG02523.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-1375C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109138022 | ||||||
| chr12:109138141
|
T | C | 5 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0039t0004g0116others(2): Show | 5 | HG01167.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-1256T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109138141 | ||||||
| chr12:109138266
|
G | A | 5 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0039t0004g0116others(2): Show | 5 | HG01167.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-1131G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109138266 | ||||||
| chr12:109138570
|
T | TA | 92 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(89): Show | 92 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-9-815dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109138570 | |||||
| chr12:109138570
|
TA | T | 92 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(89): Show | 92 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-9-815delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | 109138570 | |||||
| chr12:109138602
|
C | T | 6 | a0001c0004t0017g0003a0001c0016t0011g0274a0007c0037t0004g0073others(3): Show | 6 | HG01081.hp1 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-795C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109138602 | ||||||
| chr12:109138613
|
G | A | 1 | a0002c0043t0003g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9-784G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109138613 | ||||||
| chr12:109138861
|
A | G | 1 | a0001c0004t0002g0052 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-9-536A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | 109138861 | ||||||
| chr12:109140147
|
T | C | 161 | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0002g0261others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.653+89T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140147 | ||||||
| chr12:109140220
|
TTCCTTCC others(29): Show |
T | 1 | a0039c0080t0010g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.653+177_653+212del others(36): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140220 | |||||
| chr12:109140224
|
TTCCTTCC others(25): Show |
T | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.653+181_653+212del others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140224 | |||||
| chr12:109140228
|
TTCCTTCC others(21): Show |
T | 6 | a0001c0003t0002g0103a0001c0003t0002g0112a0002c0006t0003g0194others(3): Show | 6 | HG03490.hp1 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.653+185_653+212del others(28): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140228 | |||||
| chr12:109140231
|
C | T | 94 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.653+173C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140231 | ||||||
| chr12:109140231
|
CTTCCTTC others(33): Show |
C | 2 | a0009c0025t0001g0270a0009c0025t0001g0301 | 2 | HG01069.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.653+198_653+237del others(40): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140231 | |||||
| chr12:109140235
|
C | CTTCT | 26 | a0001c0002t0001g0283a0001c0003t0002g0104a0001c0023t0004g0121others(23): Show | 26 | HG00735.hp2 HG01074.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.653+180_653+181ins others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140235 | |||||
| chr12:109140235
|
C | T | 1 | a0007c0037t0004g0073 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.653+177C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140235 | ||||||
| chr12:109140235
|
CTTCCTTC others(29): Show |
C | 3 | a0001c0002t0008g0306a0002c0024t0003g0302a0009c0025t0001g0269 | 3 | HG01255.hp1 HG01258.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.653+198_653+233del others(36): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140235 | |||||
| chr12:109140239
|
C | T | 217 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.653+181C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140239 | ||||||
| chr12:109140239
|
CTTCCTTC others(25): Show |
C | 1 | a0007c0037t0004g0073 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.653+198_653+229del others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140239 | |||||
| chr12:109140243
|
C | T | 1 | a0001c0049t0004g0088 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.653+185C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140243 | ||||||
| chr12:109140244
|
T | A | 4 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0039t0004g0116others(1): Show | 4 | HG01167.hp2 HG02257.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+186T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140244 | ||||||
| chr12:109140247
|
CTTCCTTC others(17): Show |
C | 1 | a0001c0049t0004g0088 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.653+198_653+221del others(24): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140247 | |||||
| chr12:109140248
|
T | A | 4 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0039t0004g0116others(1): Show | 4 | HG01167.hp2 HG02257.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+190T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140248 | ||||||
| chr12:109140251
|
CTTCCATC others(13): Show |
C | 1 | a0001c0023t0001g0122 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.653+198_653+217del others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140251 | |||||
| chr12:109140252
|
T | A | 165 | a0001c0002t0001g0283a0001c0003t0002g0104a0001c0010t0002g0261others(162): Show | 165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.653+194T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140252 | ||||||
| chr12:109140255
|
C | T | 2 | a0001c0010t0001g0188a0001c0058t0016g0187 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.653+197C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140255 | ||||||
| chr12:109140256
|
A | T | 2 | a0001c0010t0001g0188a0001c0058t0016g0187 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.653+198A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140256 | ||||||
| chr12:109140256
|
ATCCTTCC others(1): Show |
A | 7 | a0004c0008t0001g0198a0006c0026t0002g0155a0006c0026t0002g0156others(4): Show | 7 | HG00323.hp1 HG02523.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.653+205_653+212del others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140256 | |||||
| chr12:109140256
|
ATCCTTCC others(9): Show |
A | 7 | a0001c0003t0004g0300a0001c0016t0009g0290a0001c0029t0002g0108others(4): Show | 7 | HG02074.hp2 HG02109.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.653+213_653+228del others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140256 | |||||
| chr12:109140256
|
ATCCTTCC others(13): Show |
A | 24 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0091others(21): Show | 24 | HG00438.hp1 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.653+213_653+232del others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140256 | |||||
| chr12:109140256
|
ATCCTTCC others(17): Show |
A | 25 | a0001c0002t0001g0081a0001c0002t0001g0098a0001c0002t0001g0109others(22): Show | 25 | HG00673.hp1 HG01074.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.653+213_653+236del others(24): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140256 | |||||
| chr12:109140256
|
ATCCTTCC others(21): Show |
A | 19 | a0001c0002t0001g0085a0001c0002t0001g0282a0001c0002t0001g0283others(16): Show | 19 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.653+213_653+240del others(28): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140256 | |||||
| chr12:109140256
|
ATCCTTCC others(25): Show |
A | 1 | a0001c0108t0001g0010 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.653+213_653+244del others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140256 | |||||
| chr12:109140256
|
ATCCTTCC others(29): Show |
A | 1 | a0018c0051t0023g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.653+213_653+248del others(36): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140256 | |||||
| chr12:109140256
|
ATCCTTCC others(33): Show |
A | 3 | a0001c0069t0002g0204a0007c0057t0004g0207a0015c0114t0004g0009 | 3 | HG03540.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.653+213_653+252del others(40): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140256 | |||||
| chr12:109140259
|
C | T | 2 | a0001c0010t0009g0186a0001c0039t0004g0116 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.653+201C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140259 | ||||||
| chr12:109140259
|
CTTCCTTC others(5): Show |
C | 11 | a0001c0002t0001g0114a0001c0002t0001g0191a0001c0003t0002g0099others(8): Show | 11 | HG00597.hp2 HG02622.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.653+213_653+224del others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140259 | |||||
| chr12:109140260
|
T | A | 49 | a0001c0013t0001g0153a0001c0045t0002g0146a0002c0043t0003g0012others(46): Show | 49 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.653+202T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140260 | ||||||
| chr12:109140263
|
C | T | 86 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0012t0002g0045others(83): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.653+205C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140263 | ||||||
| chr12:109140263
|
CTTCCTTC others(1): Show |
C | 5 | a0001c0002t0001g0035a0001c0062t0019g0288a0002c0006t0003g0111others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+213_653+220del others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140263 | |||||
| chr12:109140267
|
C | T | 2 | a0001c0010t0009g0186a0001c0039t0004g0116 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.653+209C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140267 | ||||||
| chr12:109140271
|
T | C | 4 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0039t0004g0116others(1): Show | 4 | HG01167.hp2 HG02257.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+213T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140271 | ||||||
| chr12:109140271
|
TTTCC | T | 17 | a0001c0004t0002g0050a0001c0004t0007g0001a0001c0004t0007g0011others(14): Show | 18 | HG00323.hp2 HG01884.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.653+290_653+293del others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140271 | |||||
| chr12:109140271
|
TTTCCTTC others(1): Show |
T | 15 | a0001c0018t0002g0048a0001c0018t0002g0049a0001c0018t0011g0046others(12): Show | 15 | HG01070.hp2 HG01123.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.653+286_653+293del others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140271 | |||||
| chr12:109140271
|
TTTCCTTC others(5): Show |
T | 42 | a0001c0011t0001g0013a0001c0011t0001g0157a0001c0011t0008g0018others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.653+282_653+293del others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140271 | |||||
| chr12:109140271
|
TTTCCTTC others(9): Show |
T | 37 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(34): Show | 37 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.653+278_653+293del others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140271 | |||||
| chr12:109140271
|
TTTCCTTC others(13): Show |
T | 45 | a0001c0010t0002g0261a0001c0012t0002g0262a0001c0013t0001g0153others(42): Show | 45 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.653+274_653+293del others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140271 | |||||
| chr12:109140271
|
TTTCCTTC others(17): Show |
T | 3 | a0003c0005t0002g0134a0005c0009t0003g0164a0012c0035t0004g0063 | 3 | HG03017.hp2 NA18747.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.653+270_653+293del others(24): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140271 | |||||
| chr12:109140271
|
TTTCCTTC others(21): Show |
T | 4 | a0001c0064t0009g0184a0001c0074t0004g0229a0003c0001t0001g0064others(1): Show | 4 | HG01069.hp2 HG01261.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+266_653+293del others(28): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140271 | |||||
| chr12:109140271
|
TTTCCTTC others(33): Show |
T | 1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.653+254_653+293del others(40): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140271 | |||||
| chr12:109140272
|
T | A | 1 | a0007c0030t0004g0285 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.653+214T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140272 | ||||||
| chr12:109140276
|
T | A | 3 | a0001c0010t0001g0188a0001c0058t0016g0187a0007c0030t0004g0280 | 3 | HG01167.hp2 HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.653+218T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140276 | ||||||
| chr12:109140279
|
C | T | 10 | a0001c0002t0008g0306a0002c0024t0003g0302a0004c0008t0001g0198others(7): Show | 10 | HG00323.hp1 HG01255.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.653+221C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140279 | ||||||
| chr12:109140280
|
T | A | 5 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0039t0004g0116others(2): Show | 5 | HG01167.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+222T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140280 | ||||||
| chr12:109140283
|
C | T | 2 | a0009c0025t0001g0270a0009c0025t0001g0301 | 2 | HG01069.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.653+225C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140283 | ||||||
| chr12:109140284
|
T | A | 6 | a0001c0010t0009g0186a0001c0039t0004g0116a0001c0060t0002g0272others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.653+226T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140284 | ||||||
| chr12:109140288
|
T | A | 10 | a0001c0016t0009g0290a0001c0016t0011g0274a0001c0105t0004g0296others(7): Show | 10 | HG01168.hp1 HG01169.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.653+230T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140288 | ||||||
| chr12:109140292
|
T | A | 11 | a0001c0016t0009g0287a0001c0016t0009g0305a0001c0032t0004g0291others(8): Show | 11 | HG00323.hp1 HG02523.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.653+234T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140292 | ||||||
| chr12:109140295
|
C | T | 1 | a0001c0062t0019g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.653+237C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140295 | ||||||
| chr12:109140296
|
T | A | 32 | a0001c0034t0001g0211a0001c0034t0001g0212a0001c0038t0001g0201others(29): Show | 32 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.653+238T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140296 | ||||||
| chr12:109140300
|
T | A | 40 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.653+242T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140300 | ||||||
| chr12:109140303
|
C | T | 1 | a0001c0016t0009g0290 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.653+245C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140303 | ||||||
| chr12:109140304
|
T | A | 36 | a0001c0010t0002g0261a0001c0012t0002g0045a0001c0012t0002g0250others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.653+246T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140304 | ||||||
| chr12:109140307
|
C | T | 4 | a0001c0016t0009g0287a0001c0016t0009g0305a0001c0032t0004g0291others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.653+249C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140307 | ||||||
| chr12:109140308
|
T | A | 25 | a0001c0010t0002g0261a0001c0012t0002g0262a0001c0013t0001g0256others(22): Show | 25 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.653+250T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140308 | ||||||
| chr12:109140347
|
C | CTTCCTTC others(5): Show |
1 | a0006c0120t0003g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.653+293_653+294ins others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140347 | |||||
| chr12:109140347
|
C | T | 137 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(134): Show | 137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.653+289C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140347 | ||||||
| chr12:109140485
|
C | T | 6 | a0001c0016t0009g0287a0001c0016t0009g0290a0001c0016t0009g0305others(3): Show | 6 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.653+427C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140485 | ||||||
| chr12:109140634
|
G | A | 5 | a0001c0016t0009g0287a0001c0016t0009g0290a0001c0016t0009g0305others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+576G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140634 | ||||||
| chr12:109140742
|
A | G | 73 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.653+684A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140742 | ||||||
| chr12:109140880
|
T | G | 1 | a0002c0036t0006g0223 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.653+822T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140880 | ||||||
| chr12:109140890
|
C | CT | 25 | a0001c0003t0002g0077a0001c0003t0002g0078a0001c0003t0002g0099others(22): Show | 25 | HG00597.hp1 HG01081.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.653+856dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140890 | |||||
| chr12:109140890
|
C | CTTT | 60 | a0001c0010t0002g0261a0001c0012t0002g0045a0001c0012t0002g0250others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.653+854_653+856dup others(3): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140890 | |||||
| chr12:109140890
|
C | CTTTT | 16 | a0001c0060t0002g0272a0001c0087t0001g0236a0002c0020t0003g0232others(13): Show | 16 | HG00438.hp2 HG01169.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.653+853_653+856dup others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140890 | |||||
| chr12:109140890
|
C | CTTTTT | 37 | a0001c0013t0001g0153a0001c0045t0002g0146a0002c0061t0003g0062others(34): Show | 37 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.653+852_653+856dup others(5): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140890 | |||||
| chr12:109140890
|
C | CTTTTTT | 11 | a0003c0001t0001g0143a0003c0001t0001g0149a0003c0001t0001g0154others(8): Show | 11 | HG00735.hp1 HG00741.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.653+851_653+856dup others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140890 | |||||
| chr12:109140890
|
CTTTTTTT others(3): Show |
C | 13 | a0002c0118t0005g0231a0006c0031t0004g0002a0006c0031t0004g0206others(10): Show | 13 | HG01109.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.653+847_653+856del others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109140890 | |||||
| chr12:109140921
|
G | A | 13 | a0002c0118t0005g0231a0006c0031t0004g0002a0006c0031t0004g0206others(10): Show | 13 | HG01109.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.653+863G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140921 | ||||||
| chr12:109140923
|
G | A | 8 | a0001c0004t0007g0001a0001c0004t0007g0011a0001c0004t0007g0019others(5): Show | 9 | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.653+865G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140923 | ||||||
| chr12:109140971
|
T | G | 7 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0109t0002g0276others(4): Show | 7 | HG01074.hp1 HG01175.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.653+913T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140971 | ||||||
| chr12:109140989
|
C | T | 3 | a0004c0008t0001g0218a0004c0008t0008g0219a0010c0073t0014g0208 | 3 | NA18981.hp1 NA18992.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.653+931C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109140989 | ||||||
| chr12:109141195
|
C | CCATT | 48 | a0001c0013t0001g0153a0001c0045t0002g0146a0002c0061t0003g0062others(45): Show | 48 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.653+1156_653+1159d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109141195 | |||||
| chr12:109141343
|
T | A | 6 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(3): Show | 6 | HG00323.hp1 HG02523.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.653+1285T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109141343 | ||||||
| chr12:109141383
|
G | A | 1 | a0001c0039t0004g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.653+1325G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109141383 | ||||||
| chr12:109141422
|
A | T | 1 | a0003c0001t0001g0154 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.653+1364A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109141422 | ||||||
| chr12:109141597
|
T | G | 48 | a0001c0013t0001g0153a0001c0045t0002g0146a0002c0061t0003g0062others(45): Show | 48 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.653+1539T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109141597 | ||||||
| chr12:109141681
|
T | G | 2 | a0001c0004t0002g0050a0001c0004t0002g0052 | 2 | HG00597.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.653+1623T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109141681 | ||||||
| chr12:109141971
|
G | T | 1 | a0001c0124t0012g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.653+1913G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109141971 | ||||||
| chr12:109142025
|
A | G | 1 | a0001c0107t0012g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.653+1967A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109142025 | ||||||
| chr12:109142069
|
G | A | 143 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(140): Show | 143 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.653+2011G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109142069 | ||||||
| chr12:109142082
|
T | TA | 75 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.653+2034dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109142082 | |||||
| chr12:109142177
|
A | G | 1 | a0001c0060t0002g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.653+2119A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109142177 | ||||||
| chr12:109142240
|
C | T | 20 | a0001c0124t0012g0197a0002c0118t0005g0231a0006c0026t0002g0155others(17): Show | 20 | HG00323.hp1 HG01109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.653+2182C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109142240 | ||||||
| chr12:109142400
|
A | G | 143 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(140): Show | 143 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.653+2342A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109142400 | ||||||
| chr12:109142537
|
C | T | 54 | a0001c0004t0017g0003a0001c0013t0001g0153a0001c0016t0011g0274others(51): Show | 54 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+2479C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109142537 | ||||||
| chr12:109142588
|
A | G | 6 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(3): Show | 6 | HG00323.hp1 HG02523.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.653+2530A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109142588 | ||||||
| chr12:109142589
|
C | A | 6 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(3): Show | 6 | HG00323.hp1 HG02523.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.653+2531C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109142589 | ||||||
| chr12:109142647
|
A | T | 3 | a0004c0008t0001g0227a0004c0040t0002g0215a0004c0041t0002g0224 | 3 | HG02071.hp1 NA18946.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.653+2589A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109142647 | ||||||
| chr12:109142711
|
C | T | 1 | a0001c0016t0009g0290 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.653+2653C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109142711 | ||||||
| chr12:109142785
|
T | C | 1 | a0006c0113t0004g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.653+2727T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109142785 | ||||||
| chr12:109142813
|
C | T | 1 | a0024c0091t0002g0174 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.653+2755C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109142813 | ||||||
| chr12:109142859
|
G | A | 95 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.653+2801G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109142859 | ||||||
| chr12:109143155
|
A | C | 141 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(138): Show | 141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.653+3097A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109143155 | ||||||
| chr12:109143164
|
A | G | 31 | a0001c0034t0001g0211a0001c0034t0001g0212a0001c0038t0001g0201others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.653+3106A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109143164 | ||||||
| chr12:109143182
|
CTGGGCCT others(29): Show |
C | 1 | a0002c0006t0005g0123 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.653+3129_653+3164d others(38): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109143182 | |||||
| chr12:109143462
|
C | CA | 12 | a0001c0002t0001g0283a0001c0003t0002g0094a0001c0018t0011g0046others(9): Show | 12 | HG01109.hp2 HG01123.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.653+3426dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109143462 | |||||
| chr12:109143462
|
C | CAA | 80 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0081others(77): Show | 80 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.653+3425_653+3426d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109143462 | |||||
| chr12:109143462
|
C | CAAA | 24 | a0001c0002t0001g0035a0001c0002t0001g0114a0001c0002t0001g0235others(21): Show | 24 | HG00438.hp1 HG01069.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.653+3424_653+3426d others(5): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109143462 | |||||
| chr12:109143462
|
CA | C | 71 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(68): Show | 71 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.653+3426delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109143462 | |||||
| chr12:109143462
|
CAA | C | 6 | a0001c0013t0001g0256a0001c0038t0001g0201a0002c0070t0005g0199others(3): Show | 6 | HG00280.hp2 HG02145.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.653+3425_653+3426d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109143462 | |||||
| chr12:109143462
|
CAAAAAAA others(2): Show |
C | 47 | a0001c0013t0001g0153a0001c0045t0002g0146a0002c0061t0003g0062others(44): Show | 47 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.653+3418_653+3426d others(11): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109143462 | |||||
| chr12:109143568
|
G | A | 264 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.653+3510G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109143568 | ||||||
| chr12:109143625
|
G | A | 2 | a0001c0069t0002g0204a0002c0092t0010g0192 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.653+3567G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109143625 | ||||||
| chr12:109143688
|
A | G | 98 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(95): Show | 98 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.653+3630A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109143688 | ||||||
| chr12:109143711
|
G | A | 8 | a0001c0004t0017g0003a0001c0069t0002g0204a0002c0092t0010g0192others(5): Show | 8 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.653+3653G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109143711 | ||||||
| chr12:109143828
|
G | A | 2 | a0001c0049t0001g0289a0002c0006t0005g0284 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.653+3770G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109143828 | ||||||
| chr12:109144017
|
A | T | 1 | a0001c0069t0002g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.653+3959A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144017 | ||||||
| chr12:109144021
|
A | T | 1 | a0001c0069t0002g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.653+3963A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144021 | ||||||
| chr12:109144089
|
G | A | 1 | a0007c0101t0002g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.653+4031G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144089 | ||||||
| chr12:109144208
|
G | A | 1 | a0006c0078t0001g0181 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.653+4150G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144208 | ||||||
| chr12:109144209
|
A | G | 1 | a0006c0078t0001g0181 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.653+4151A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144209 | ||||||
| chr12:109144316
|
A | T | 3 | a0001c0004t0002g0054a0001c0011t0001g0056a0002c0007t0003g0055 | 3 | HG01884.hp2 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.653+4258A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144316 | ||||||
| chr12:109144346
|
C | A | 4 | a0001c0004t0017g0003a0007c0037t0004g0073a0027c0065t0005g0225others(1): Show | 4 | HG01081.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+4288C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144346 | ||||||
| chr12:109144400
|
G | T | 241 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.653+4342G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144400 | ||||||
| chr12:109144492
|
C | T | 1 | a0002c0017t0003g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.653+4434C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144492 | ||||||
| chr12:109144513
|
A | G | 240 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.653+4455A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144513 | ||||||
| chr12:109144518
|
A | G | 2 | a0001c0069t0002g0204a0002c0092t0010g0192 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.653+4460A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144518 | ||||||
| chr12:109144564
|
A | C | 1 | a0015c0114t0004g0009 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.653+4506A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144564 | ||||||
| chr12:109144687
|
G | A | 7 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(4): Show | 7 | HG01891.hp1 HG02280.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.653+4629G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144687 | ||||||
| chr12:109144750
|
C | CT | 80 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0081others(77): Show | 80 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.653+4695dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109144750 | |||||
| chr12:109144750
|
C | CTT | 13 | a0001c0002t0008g0306a0001c0060t0002g0272a0001c0108t0001g0010others(10): Show | 13 | HG00323.hp1 HG01884.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.653+4694_653+4695d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109144750 | |||||
| chr12:109144750
|
C | CTTT | 71 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(68): Show | 71 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.653+4693_653+4695d others(5): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109144750 | |||||
| chr12:109144750
|
C | CTTTT | 50 | a0001c0013t0001g0153a0001c0045t0002g0146a0001c0087t0001g0236others(47): Show | 50 | HG00438.hp2 HG00609.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.653+4695_653+4696i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109144750 | |||||
| chr12:109144750
|
C | CTTTTT | 12 | a0003c0001t0001g0132a0003c0001t0001g0140a0003c0001t0001g0141others(9): Show | 12 | HG00639.hp1 HG02738.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.653+4695_653+4696i others(7): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109144750 | |||||
| chr12:109144750
|
CTTTCTT | C | 6 | a0001c0105t0004g0296a0001c0106t0001g0293a0002c0006t0005g0294others(3): Show | 6 | HG01891.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.653+4696_653+4701d others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109144750 | |||||
| chr12:109144750
|
CTTTCTTT others(5): Show |
C | 2 | a0007c0037t0004g0073a0039c0080t0010g0071 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.653+4696_653+4707d others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109144750 | |||||
| chr12:109144754
|
C | T | 248 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.653+4696C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144754 | ||||||
| chr12:109144757
|
T | TC | 16 | a0001c0002t0001g0035a0001c0002t0001g0191a0001c0002t0001g0235others(13): Show | 16 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.653+4699_653+4700i others(3): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144757 | ||||||
| chr12:109144758
|
T | C | 1 | a0001c0003t0002g0099 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.653+4700T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144758 | ||||||
| chr12:109144767
|
T | G | 6 | a0001c0016t0009g0287a0001c0016t0009g0290a0001c0016t0009g0305others(3): Show | 6 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.653+4709T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144767 | ||||||
| chr12:109144798
|
A | G | 4 | a0001c0002t0001g0235a0001c0002t0001g0241a0001c0002t0001g0242others(1): Show | 4 | HG02027.hp2 NA18950.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.653+4740A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144798 | ||||||
| chr12:109144800
|
G | T | 5 | a0003c0001t0001g0064a0003c0001t0001g0143a0003c0005t0002g0059others(2): Show | 5 | HG00639.hp1 HG00741.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+4742G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144800 | ||||||
| chr12:109144994
|
G | A | 1 | a0014c0079t0004g0180 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.653+4936G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109144994 | ||||||
| chr12:109145014
|
G | A | 8 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.653+4956G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109145014 | ||||||
| chr12:109145061
|
C | T | 1 | a0002c0092t0010g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.653+5003C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109145061 | ||||||
| chr12:109145163
|
T | TGAATCTC others(1): Show |
82 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(79): Show | 82 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.653+5105_653+5106i others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109145163 | ||||||
| chr12:109145170
|
T | C | 98 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(95): Show | 98 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.653+5112T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109145170 | ||||||
| chr12:109145218
|
G | A | 1 | a0026c0066t0015g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.653+5160G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109145218 | ||||||
| chr12:109145252
|
A | AG | 6 | a0001c0016t0009g0287a0001c0016t0009g0290a0001c0016t0009g0305others(3): Show | 6 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.653+5198dupG | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109145252 | |||||
| chr12:109145391
|
C | A | 1 | a0001c0013t0001g0153 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.653+5333C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109145391 | ||||||
| chr12:109145392
|
G | A | 1 | a0001c0003t0002g0077 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.653+5334G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109145392 | ||||||
| chr12:109145769
|
G | A | 2 | a0001c0023t0004g0121a0002c0097t0003g0124 | 2 | HG00735.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.653+5711G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109145769 | ||||||
| chr12:109145776
|
G | A | 1 | a0001c0011t0001g0008 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.653+5718G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109145776 | ||||||
| chr12:109145836
|
T | TA | 12 | a0001c0002t0008g0306a0001c0004t0002g0054a0001c0011t0001g0056others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.653+5793dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109145836 | |||||
| chr12:109145924
|
A | G | 228 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.653+5866A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109145924 | ||||||
| chr12:109145931
|
C | G | 80 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.653+5873C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109145931 | ||||||
| chr12:109145988
|
A | G | 264 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.653+5930A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109145988 | ||||||
| chr12:109146143
|
G | A | 2 | a0001c0002t0001g0282a0001c0003t0004g0300 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.653+6085G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109146143 | ||||||
| chr12:109146233
|
C | T | 4 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(1): Show | 4 | HG03139.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+6175C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109146233 | ||||||
| chr12:109146238
|
A | G | 1 | a0026c0066t0015g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.653+6180A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109146238 | ||||||
| chr12:109146297
|
T | C | 1 | a0007c0057t0004g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.653+6239T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109146297 | ||||||
| chr12:109146329
|
G | A | 4 | a0001c0004t0017g0003a0007c0037t0004g0073a0027c0065t0005g0225others(1): Show | 4 | HG01081.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+6271G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109146329 | ||||||
| chr12:109146550
|
A | G | 91 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(88): Show | 91 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.653+6492A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109146550 | ||||||
| chr12:109146673
|
T | G | 1 | a0001c0108t0001g0010 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.653+6615T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109146673 | ||||||
| chr12:109147048
|
C | T | 2 | a0007c0037t0004g0073a0039c0080t0010g0071 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.653+6990C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109147048 | ||||||
| chr12:109147132
|
A | G | 1 | a0007c0057t0004g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.653+7074A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109147132 | ||||||
| chr12:109147186
|
T | C | 54 | a0001c0013t0001g0153a0001c0045t0002g0146a0001c0069t0002g0204others(51): Show | 54 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+7128T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109147186 | ||||||
| chr12:109147222
|
TTTTG | T | 3 | a0013c0033t0002g0185a0013c0033t0002g0189a0026c0066t0015g0115 | 3 | HG01168.hp1 HG01169.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.653+7188_653+7191d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109147222 | |||||
| chr12:109147391
|
C | CT | 15 | a0001c0002t0008g0306a0001c0003t0002g0097a0001c0004t0007g0011others(12): Show | 15 | HG00438.hp1 HG00438.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.653+7357dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109147391 | |||||
| chr12:109147391
|
CT | C | 58 | a0001c0011t0001g0157a0001c0013t0001g0153a0001c0032t0004g0291others(55): Show | 58 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.653+7357delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109147391 | |||||
| chr12:109147655
|
T | C | 10 | a0001c0004t0017g0003a0001c0016t0009g0287a0001c0016t0009g0290others(7): Show | 10 | HG01081.hp1 HG02109.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.653+7597T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109147655 | ||||||
| chr12:109147881
|
A | G | 54 | a0001c0013t0001g0153a0001c0045t0002g0146a0001c0069t0002g0204others(51): Show | 54 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+7823A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109147881 | ||||||
| chr12:109148085
|
G | A | 54 | a0001c0013t0001g0153a0001c0045t0002g0146a0001c0069t0002g0204others(51): Show | 54 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+8027G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109148085 | ||||||
| chr12:109148246
|
A | G | 54 | a0001c0013t0001g0153a0001c0045t0002g0146a0001c0069t0002g0204others(51): Show | 54 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+8188A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109148246 | ||||||
| chr12:109148352
|
T | C | 10 | a0001c0004t0017g0003a0001c0016t0009g0287a0001c0016t0009g0290others(7): Show | 10 | HG01081.hp1 HG02109.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.653+8294T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109148352 | ||||||
| chr12:109148494
|
G | A | 9 | a0001c0002t0001g0283a0001c0048t0002g0281a0001c0048t0004g0307others(6): Show | 9 | HG02486.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.653+8436G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109148494 | ||||||
| chr12:109148674
|
A | G | 91 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(88): Show | 91 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.653+8616A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109148674 | ||||||
| chr12:109148721
|
A | T | 1 | a0001c0038t0001g0029 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.653+8663A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109148721 | ||||||
| chr12:109148804
|
G | A | 54 | a0001c0013t0001g0153a0001c0045t0002g0146a0001c0069t0002g0204others(51): Show | 54 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+8746G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109148804 | ||||||
| chr12:109148961
|
A | G | 54 | a0001c0013t0001g0153a0001c0045t0002g0146a0001c0069t0002g0204others(51): Show | 54 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+8903A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109148961 | ||||||
| chr12:109149142
|
G | A | 1 | a0002c0014t0003g0106 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.653+9084G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109149142 | ||||||
| chr12:109149255
|
G | T | 3 | a0001c0016t0011g0274a0001c0124t0012g0197a0007c0057t0004g0207 | 3 | HG02965.hp1 HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.653+9197G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109149255 | ||||||
| chr12:109149295
|
G | T | 5 | a0001c0018t0002g0048a0001c0018t0002g0049a0001c0018t0011g0046others(2): Show | 5 | HG01070.hp2 HG01123.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+9237G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109149295 | ||||||
| chr12:109149365
|
A | C | 7 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(4): Show | 7 | HG01891.hp1 HG02280.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.653+9307A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109149365 | ||||||
| chr12:109149490
|
G | A | 4 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(1): Show | 4 | HG03139.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+9432G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109149490 | ||||||
| chr12:109149640
|
G | T | 3 | a0001c0013t0001g0153a0005c0009t0006g0148a0005c0009t0006g0177 | 3 | NA18961.hp2 NA18966.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.653+9582G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109149640 | ||||||
| chr12:109149670
|
C | T | 48 | a0001c0013t0001g0153a0001c0045t0002g0146a0002c0061t0003g0062others(45): Show | 48 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.653+9612C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109149670 | ||||||
| chr12:109149719
|
C | T | 2 | a0001c0002t0001g0282a0001c0003t0004g0300 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.653+9661C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109149719 | ||||||
| chr12:109149831
|
G | C | 1 | a0018c0051t0023g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.653+9773G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109149831 | ||||||
| chr12:109149909
|
G | A | 48 | a0001c0013t0001g0153a0001c0045t0002g0146a0002c0061t0003g0062others(45): Show | 48 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.653+9851G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109149909 | ||||||
| chr12:109149927
|
G | A | 156 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(153): Show | 156 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.653+9869G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109149927 | ||||||
| chr12:109150083
|
C | G | 1 | a0001c0002t0001g0283 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.653+10025C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109150083 | ||||||
| chr12:109150121
|
C | T | 1 | a0003c0001t0001g0087 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.653+10063C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109150121 | ||||||
| chr12:109150128
|
C | T | 4 | a0006c0031t0004g0002a0006c0031t0004g0206a0006c0031t0013g0205others(1): Show | 4 | HG01109.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.653+10070C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109150128 | ||||||
| chr12:109150162
|
G | T | 1 | a0002c0043t0003g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.653+10104G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109150162 | ||||||
| chr12:109150377
|
A | G | 1 | a0014c0079t0004g0180 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.653+10319A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109150377 | ||||||
| chr12:109150627
|
T | C | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.653+10569T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109150627 | ||||||
| chr12:109150655
|
T | A | 1 | a0001c0002t0001g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.653+10597T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109150655 | ||||||
| chr12:109150675
|
C | T | 1 | a0017c0123t0015g0058 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.653+10617C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109150675 | ||||||
| chr12:109150770
|
A | G | 1 | a0012c0035t0004g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.653+10712A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109150770 | ||||||
| chr12:109150836
|
C | T | 1 | a0002c0118t0005g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.653+10778C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109150836 | ||||||
| chr12:109150902
|
C | G | 91 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(88): Show | 91 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.653+10844C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109150902 | ||||||
| chr12:109150903
|
T | G | 60 | a0001c0013t0001g0153a0001c0045t0002g0146a0001c0069t0002g0204others(57): Show | 60 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.653+10845T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109150903 | ||||||
| chr12:109150982
|
C | CT | 39 | a0001c0002t0008g0306a0001c0012t0002g0045a0001c0012t0002g0250others(36): Show | 39 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.653+10938dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109150982 | |||||
| chr12:109150982
|
C | CTT | 46 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0022t0004g0004others(43): Show | 46 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.653+10937_653+1093 others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109150982 | |||||
| chr12:109150982
|
CTTTTT | C | 60 | a0001c0013t0001g0153a0001c0045t0002g0146a0001c0069t0002g0204others(57): Show | 60 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.653+10934_653+1093 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109150982 | |||||
| chr12:109151068
|
G | A | 2 | a0013c0033t0002g0185a0013c0033t0002g0189 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.653+11010G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151068 | ||||||
| chr12:109151072
|
G | A | 1 | a0001c0109t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.653+11014G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151072 | ||||||
| chr12:109151086
|
G | A | 1 | a0001c0064t0009g0184 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.653+11028G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151086 | ||||||
| chr12:109151171
|
G | A | 1 | a0024c0091t0002g0174 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.653+11113G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151171 | ||||||
| chr12:109151219
|
A | G | 248 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.653+11161A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151219 | ||||||
| chr12:109151375
|
C | T | 1 | a0001c0018t0002g0049 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.653+11317C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151375 | ||||||
| chr12:109151455
|
A | T | 8 | a0001c0069t0002g0204a0002c0092t0010g0192a0006c0026t0002g0155others(5): Show | 8 | HG00323.hp1 HG02523.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.653+11397A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151455 | ||||||
| chr12:109151599
|
G | T | 7 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(4): Show | 7 | HG01891.hp1 HG02280.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.653+11541G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151599 | ||||||
| chr12:109151659
|
G | A | 26 | a0001c0034t0001g0211a0001c0034t0001g0212a0002c0036t0006g0223others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.653+11601G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151659 | ||||||
| chr12:109151771
|
A | G | 1 | a0002c0006t0003g0107 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.653+11713A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151771 | ||||||
| chr12:109151788
|
A | G | 70 | a0001c0004t0017g0003a0001c0013t0001g0153a0001c0016t0009g0287others(67): Show | 70 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.653+11730A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151788 | ||||||
| chr12:109151856
|
G | T | 77 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(74): Show | 77 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.653+11798G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151856 | ||||||
| chr12:109151876
|
G | A | 1 | a0001c0107t0012g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.653+11818G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151876 | ||||||
| chr12:109151939
|
G | A | 8 | a0003c0001t0001g0149a0003c0005t0002g0129a0003c0005t0002g0131others(5): Show | 8 | HG00735.hp1 HG01109.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.653+11881G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151939 | ||||||
| chr12:109151963
|
C | T | 17 | a0001c0004t0017g0003a0001c0016t0009g0287a0001c0016t0009g0290others(14): Show | 17 | HG00323.hp1 HG01081.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.653+11905C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109151963 | ||||||
| chr12:109152209
|
A | G | 3 | a0003c0005t0002g0245a0005c0009t0003g0304a0005c0019t0003g0271 | 3 | HG00621.hp2 NA18955.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.653+12151A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109152209 | ||||||
| chr12:109152215
|
C | G | 2 | a0001c0054t0001g0203a0002c0053t0005g0033 | 2 | HG01943.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.653+12157C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109152215 | ||||||
| chr12:109152411
|
A | G | 97 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(94): Show | 97 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.653+12353A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109152411 | ||||||
| chr12:109152515
|
G | A | 64 | a0001c0004t0017g0003a0001c0013t0001g0153a0001c0045t0002g0146others(61): Show | 64 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.653+12457G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109152515 | ||||||
| chr12:109152611
|
C | T | 1 | a0004c0008t0001g0198 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.653+12553C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109152611 | ||||||
| chr12:109152624
|
T | TTTTC | 65 | a0001c0010t0002g0261a0001c0010t0009g0186a0001c0012t0002g0250others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.653+12582_653+1258 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109152624 | |||||
| chr12:109152631
|
T | TCTTC | 9 | a0001c0002t0001g0085a0001c0002t0001g0091a0001c0003t0002g0094others(6): Show | 9 | HG00099.hp2 HG00558.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+12576_653+1257 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109152631 | |||||
| chr12:109152635
|
T | C | 84 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(81): Show | 84 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.653+12577T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109152635 | ||||||
| chr12:109152640
|
C | CT | 14 | a0001c0011t0008g0018a0001c0018t0011g0046a0001c0074t0004g0229others(11): Show | 14 | HG01123.hp1 HG01261.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.653+12607dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109152640 | |||||
| chr12:109152640
|
C | CTTTCT | 78 | a0001c0002t0001g0035a0001c0002t0001g0079a0001c0002t0001g0081others(75): Show | 78 | HG00438.hp1 HG00597.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.653+12585_653+1258 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109152640 | |||||
| chr12:109152640
|
C | CTTTCTT | 13 | a0001c0002t0001g0075a0001c0002t0001g0235a0001c0003t0002g0244others(10): Show | 13 | HG00423.hp2 HG01106.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.653+12585_653+1258 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109152640 | |||||
| chr12:109152640
|
CT | C | 11 | a0001c0004t0017g0003a0001c0010t0002g0021a0001c0039t0004g0039others(8): Show | 11 | HG01069.hp2 HG01081.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.653+12607delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109152640 | |||||
| chr12:109152640
|
CTTTTTTT | C | 14 | a0002c0118t0005g0231a0006c0031t0004g0002a0006c0031t0004g0206others(11): Show | 14 | HG01109.hp2 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.653+12601_653+1260 others(11): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109152640 | |||||
| chr12:109152641
|
T | TTTC | 8 | a0001c0012t0002g0045a0001c0109t0002g0276a0002c0020t0003g0120others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.653+12585_653+1258 others(7): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109152641 | |||||
| chr12:109152646
|
T | C | 1 | a0001c0016t0009g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.653+12588T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109152646 | ||||||
| chr12:109152647
|
T | C | 5 | a0001c0016t0009g0287a0001c0016t0009g0290a0001c0032t0004g0291others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+12589T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109152647 | ||||||
| chr12:109152799
|
C | G | 6 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(3): Show | 6 | HG00323.hp1 HG02523.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.653+12741C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109152799 | ||||||
| chr12:109152981
|
T | A | 2 | a0013c0033t0002g0185a0013c0033t0002g0189 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.653+12923T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109152981 | ||||||
| chr12:109153047
|
C | T | 4 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0111t0001g0275others(1): Show | 4 | HG01074.hp1 HG01175.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+12989C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109153047 | ||||||
| chr12:109153364
|
T | G | 1 | a0002c0017t0003g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.653+13306T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109153364 | ||||||
| chr12:109153501
|
G | A | 1 | a0003c0005t0002g0129 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.654-13360G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109153501 | ||||||
| chr12:109153553
|
G | C | 7 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0109t0002g0276others(4): Show | 7 | HG01074.hp1 HG01175.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.654-13308G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109153553 | ||||||
| chr12:109153564
|
T | G | 91 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(88): Show | 91 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.654-13297T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109153564 | ||||||
| chr12:109153876
|
C | T | 157 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(154): Show | 157 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.654-12985C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109153876 | ||||||
| chr12:109154201
|
C | T | 1 | a0001c0004t0017g0003 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.654-12660C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109154201 | ||||||
| chr12:109154364
|
C | T | 1 | a0001c0010t0002g0261 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.654-12497C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109154364 | ||||||
| chr12:109154678
|
T | C | 70 | a0001c0004t0017g0003a0001c0013t0001g0153a0001c0016t0009g0287others(67): Show | 70 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.654-12183T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109154678 | ||||||
| chr12:109154753
|
C | G | 65 | a0001c0004t0017g0003a0001c0013t0001g0153a0001c0045t0002g0146others(62): Show | 65 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.654-12108C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109154753 | ||||||
| chr12:109154800
|
G | A | 1 | a0002c0014t0003g0015 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.654-12061G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109154800 | ||||||
| chr12:109155047
|
C | G | 51 | a0001c0013t0001g0153a0001c0045t0002g0146a0001c0069t0002g0204others(48): Show | 51 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.654-11814C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109155047 | ||||||
| chr12:109155201
|
G | A | 3 | a0001c0016t0011g0274a0001c0124t0012g0197a0007c0057t0004g0207 | 3 | HG02965.hp1 HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.654-11660G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109155201 | ||||||
| chr12:109155582
|
C | A | 1 | a0001c0004t0017g0003 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.654-11279C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109155582 | ||||||
| chr12:109155585
|
C | CT | 6 | a0001c0003t0002g0077a0001c0087t0001g0236a0001c0089t0002g0162others(3): Show | 6 | HG00438.hp2 HG01175.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.654-11264dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109155585 | |||||
| chr12:109155865
|
C | T | 3 | a0002c0007t0003g0037a0002c0007t0003g0041a0002c0017t0024g0044 | 3 | HG02572.hp1 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.654-10996C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109155865 | ||||||
| chr12:109156268
|
G | A | 1 | a0012c0035t0004g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.654-10593G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156268 | ||||||
| chr12:109156285
|
T | C | 1 | a0001c0109t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.654-10576T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156285 | ||||||
| chr12:109156341
|
G | T | 1 | a0001c0002t0001g0283 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.654-10520G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156341 | ||||||
| chr12:109156387
|
G | A | 2 | a0001c0011t0001g0157a0032c0059t0002g0038 | 2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.654-10474G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156387 | ||||||
| chr12:109156389
|
A | G | 1 | a0002c0020t0003g0232 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.654-10472A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156389 | ||||||
| chr12:109156587
|
GT | G | 180 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.654-10257delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109156587 | |||||
| chr12:109156587
|
GTT | G | 63 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.654-10258_654-1025 others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109156587 | |||||
| chr12:109156603
|
T | G | 2 | a0004c0040t0002g0213a0027c0065t0005g0225 | 2 | HG01081.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.654-10258T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156603 | ||||||
| chr12:109156604
|
T | G | 142 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.654-10257T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156604 | ||||||
| chr12:109156606
|
G | C | 92 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(89): Show | 92 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.654-10255G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156606 | ||||||
| chr12:109156611
|
G | A | 93 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(90): Show | 93 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.654-10250G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156611 | ||||||
| chr12:109156612
|
G | A | 3 | a0002c0007t0003g0037a0002c0007t0003g0041a0002c0017t0024g0044 | 3 | HG02572.hp1 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.654-10249G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156612 | ||||||
| chr12:109156638
|
A | G | 58 | a0001c0013t0001g0153a0001c0045t0002g0146a0001c0050t0001g0277others(55): Show | 58 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.654-10223A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156638 | ||||||
| chr12:109156778
|
G | A | 4 | a0001c0039t0004g0116a0001c0064t0009g0184a0001c0074t0004g0229others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.654-10083G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156778 | ||||||
| chr12:109156811
|
T | C | 2 | a0001c0039t0004g0116a0001c0064t0009g0184 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.654-10050T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156811 | ||||||
| chr12:109156851
|
C | G | 1 | a0001c0002t0008g0306 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.654-10010C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156851 | ||||||
| chr12:109156975
|
A | G | 93 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(90): Show | 93 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.654-9886A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156975 | ||||||
| chr12:109156976
|
G | C | 93 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(90): Show | 93 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.654-9885G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109156976 | ||||||
| chr12:109157016
|
G | A | 93 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(90): Show | 93 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.654-9845G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109157016 | ||||||
| chr12:109157251
|
C | G | 8 | a0001c0002t0001g0035a0001c0002t0001g0191a0001c0003t0002g0099others(5): Show | 8 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-9610C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109157251 | ||||||
| chr12:109157272
|
G | GTTA | 5 | a0001c0039t0004g0116a0001c0064t0009g0184a0001c0074t0004g0229others(2): Show | 5 | HG01891.hp1 HG02071.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.654-9564_654-9562d others(5): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109157272 | |||||
| chr12:109157272
|
G | GTTATTA | 110 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0081others(107): Show | 110 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.654-9567_654-9562d others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109157272 | |||||
| chr12:109157272
|
G | GTTATTAT others(2): Show |
12 | a0001c0002t0001g0079a0001c0002t0001g0091a0001c0002t0001g0282others(9): Show | 12 | HG00741.hp1 HG01070.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.654-9570_654-9562d others(11): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109157272 | |||||
| chr12:109157272
|
G | GTTATTAT others(5): Show |
14 | a0001c0016t0009g0287a0001c0016t0009g0290a0001c0016t0009g0305others(11): Show | 14 | HG00609.hp2 HG01433.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.654-9573_654-9562d others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109157272 | |||||
| chr12:109157272
|
G | GTTATTAT others(8): Show |
78 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0013t0001g0153others(75): Show | 78 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.654-9576_654-9562d others(17): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109157272 | |||||
| chr12:109157272
|
G | GTTATTAT others(11): Show |
18 | a0001c0004t0017g0003a0001c0022t0004g0004a0001c0022t0004g0005others(15): Show | 18 | HG02145.hp2 HG02523.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.654-9579_654-9562d others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109157272 | |||||
| chr12:109157272
|
G | GTTATTAT others(14): Show |
3 | a0002c0070t0005g0199a0005c0019t0006g0076a0021c0068t0001g0202 | 3 | HG03516.hp1 NA18522.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.654-9582_654-9562d others(23): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109157272 | |||||
| chr12:109157272
|
G | GTTGTTAT others(5): Show |
12 | a0002c0118t0005g0231a0006c0031t0004g0002a0006c0031t0004g0206others(9): Show | 12 | HG01109.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.654-9587_654-9586i others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109157272 | |||||
| chr12:109157272
|
G | GTTGTTAT others(8): Show |
2 | a0008c0015t0005g0168a0008c0044t0025g0166 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.654-9587_654-9586i others(17): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109157272 | |||||
| chr12:109157305
|
A | C | 7 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0109t0002g0276others(4): Show | 7 | HG01074.hp1 HG01175.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.654-9556A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109157305 | ||||||
| chr12:109157488
|
T | G | 1 | a0002c0092t0010g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.654-9373T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109157488 | ||||||
| chr12:109157581
|
C | T | 153 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(150): Show | 153 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.654-9280C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109157581 | ||||||
| chr12:109157590
|
C | T | 72 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.654-9271C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109157590 | ||||||
| chr12:109157687
|
C | G | 1 | a0002c0036t0006g0223 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.654-9174C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109157687 | ||||||
| chr12:109157771
|
C | G | 58 | a0001c0013t0001g0153a0001c0045t0002g0146a0001c0050t0001g0277others(55): Show | 58 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.654-9090C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109157771 | ||||||
| chr12:109157904
|
G | A | 4 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(1): Show | 4 | HG03139.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-8957G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109157904 | ||||||
| chr12:109158046
|
C | T | 171 | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0002g0261others(168): Show | 171 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.654-8815C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109158046 | ||||||
| chr12:109158066
|
C | G | 2 | a0013c0033t0002g0185a0013c0033t0002g0189 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.654-8795C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109158066 | ||||||
| chr12:109158218
|
G | A | 265 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.654-8643G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109158218 | ||||||
| chr12:109158366
|
AT | A | 151 | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0002g0261others(148): Show | 151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.654-8480delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109158366 | |||||
| chr12:109158366
|
ATT | A | 108 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.654-8481_654-8480d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109158366 | |||||
| chr12:109158391
|
A | G | 6 | a0001c0016t0009g0287a0001c0016t0009g0290a0001c0016t0009g0305others(3): Show | 6 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.654-8470A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109158391 | ||||||
| chr12:109158513
|
C | T | 1 | a0033c0063t0010g0117 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.654-8348C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109158513 | ||||||
| chr12:109158526
|
A | G | 1 | a0003c0001t0001g0147 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.654-8335A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109158526 | ||||||
| chr12:109158638
|
T | C | 3 | a0001c0064t0009g0184a0001c0074t0004g0229a0035c0076t0010g0267 | 3 | HG01891.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.654-8223T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109158638 | ||||||
| chr12:109158701
|
C | T | 93 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(90): Show | 93 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.654-8160C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109158701 | ||||||
| chr12:109158702
|
G | A | 2 | a0007c0037t0004g0073a0039c0080t0010g0071 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.654-8159G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109158702 | ||||||
| chr12:109158753
|
C | T | 1 | a0003c0001t0001g0178 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.654-8108C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109158753 | ||||||
| chr12:109158910
|
G | A | 58 | a0001c0013t0001g0153a0001c0045t0002g0146a0001c0050t0001g0277others(55): Show | 58 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.654-7951G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109158910 | ||||||
| chr12:109158975
|
G | GAAAC | 278 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.654-7881_654-7878d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109158975 | |||||
| chr12:109158997
|
A | G | 3 | a0008c0015t0005g0171a0008c0015t0005g0172a0008c0015t0005g0173 | 3 | HG02280.hp1 HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.654-7864A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109158997 | ||||||
| chr12:109159319
|
C | T | 1 | a0018c0051t0023g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.654-7542C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109159319 | ||||||
| chr12:109159352
|
A | G | 265 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.654-7509A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109159352 | ||||||
| chr12:109159507
|
A | G | 10 | a0001c0002t0001g0283a0001c0048t0002g0281a0001c0048t0004g0307others(7): Show | 10 | HG02109.hp1 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.654-7354A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109159507 | ||||||
| chr12:109159700
|
G | A | 79 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(76): Show | 79 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.654-7161G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109159700 | ||||||
| chr12:109159718
|
C | T | 5 | a0001c0004t0017g0003a0007c0037t0004g0073a0026c0066t0015g0115others(2): Show | 5 | HG01081.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.654-7143C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109159718 | ||||||
| chr12:109159754
|
T | C | 1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.654-7107T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109159754 | ||||||
| chr12:109159774
|
C | T | 7 | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0009g0186others(4): Show | 7 | HG01081.hp1 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.654-7087C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109159774 | ||||||
| chr12:109160047
|
G | C | 1 | a0002c0007t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.654-6814G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109160047 | ||||||
| chr12:109160089
|
C | CA | 27 | a0001c0002t0001g0235a0001c0003t0002g0099a0001c0003t0002g0103others(24): Show | 27 | HG00423.hp1 HG00558.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.654-6756dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109160089 | |||||
| chr12:109160099
|
A | C | 19 | a0001c0016t0011g0274a0001c0058t0016g0187a0001c0124t0012g0197others(16): Show | 19 | HG01109.hp2 HG01167.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.654-6762A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109160099 | ||||||
| chr12:109160101
|
A | G | 2 | a0001c0039t0004g0116a0001c0064t0009g0184 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.654-6760A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109160101 | ||||||
| chr12:109160125
|
A | C | 142 | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(139): Show | 142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.654-6736A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109160125 | ||||||
| chr12:109160373
|
G | T | 1 | a0001c0002t0001g0235 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.654-6488G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109160373 | ||||||
| chr12:109160411
|
G | T | 1 | a0001c0004t0017g0003 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.654-6450G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109160411 | ||||||
| chr12:109160415
|
C | T | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.654-6446C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109160415 | ||||||
| chr12:109160600
|
G | A | 1 | a0001c0013t0001g0153 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.654-6261G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109160600 | ||||||
| chr12:109160744
|
A | C | 101 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(98): Show | 101 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.654-6117A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109160744 | ||||||
| chr12:109160751
|
T | C | 230 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(227): Show | 230 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.654-6110T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109160751 | ||||||
| chr12:109160752
|
G | A | 6 | a0001c0054t0001g0203a0001c0055t0001g0226a0001c0095t0001g0133others(3): Show | 6 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.654-6109G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109160752 | ||||||
| chr12:109160926
|
G | T | 1 | a0001c0002t0001g0035 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.654-5935G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109160926 | ||||||
| chr12:109160994
|
T | C | 1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.654-5867T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109160994 | ||||||
| chr12:109161073
|
G | A | 2 | a0001c0003t0002g0099a0002c0006t0003g0111 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.654-5788G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109161073 | ||||||
| chr12:109161083
|
A | G | 1 | a0009c0103t0004g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.654-5778A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109161083 | ||||||
| chr12:109161084
|
C | T | 19 | a0001c0058t0016g0187a0006c0026t0002g0155a0006c0026t0002g0156others(16): Show | 19 | HG00323.hp1 HG01109.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.654-5777C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109161084 | ||||||
| chr12:109161104
|
G | A | 1 | a0006c0026t0016g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.654-5757G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109161104 | ||||||
| chr12:109161223
|
A | T | 1 | a0001c0074t0004g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.654-5638A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109161223 | ||||||
| chr12:109161282
|
G | A | 1 | a0001c0002t0001g0085 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.654-5579G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109161282 | ||||||
| chr12:109161367
|
AC | A | 4 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(1): Show | 4 | HG03139.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-5490delC | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109161367 | |||||
| chr12:109161446
|
G | C | 1 | a0009c0103t0004g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.654-5415G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109161446 | ||||||
| chr12:109161535
|
G | T | 129 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(126): Show | 129 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.654-5326G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109161535 | ||||||
| chr12:109161639
|
G | A | 20 | a0001c0058t0016g0187a0006c0026t0002g0155a0006c0026t0002g0156others(17): Show | 20 | HG00323.hp1 HG01109.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.654-5222G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109161639 | ||||||
| chr12:109161731
|
T | TTG | 95 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(92): Show | 95 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.654-5124_654-5123d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109161731 | |||||
| chr12:109161731
|
T | TTGTG | 23 | a0001c0004t0017g0003a0001c0016t0009g0287a0001c0016t0009g0290others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.654-5126_654-5123d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109161731 | |||||
| chr12:109161735
|
GTGTA | G | 8 | a0001c0105t0004g0296a0001c0106t0001g0293a0002c0006t0005g0294others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-5122_654-5119d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109161735 | |||||
| chr12:109161739
|
A | G | 121 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(118): Show | 121 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.654-5122A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109161739 | ||||||
| chr12:109161860
|
T | C | 129 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(126): Show | 129 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.654-5001T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109161860 | ||||||
| chr12:109161906
|
C | T | 1 | a0001c0074t0004g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.654-4955C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109161906 | ||||||
| chr12:109161931
|
G | C | 1 | a0003c0001t0001g0087 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.654-4930G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109161931 | ||||||
| chr12:109161952
|
AC | A | 98 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(95): Show | 98 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.654-4907delC | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109161952 | |||||
| chr12:109161980
|
C | CT | 15 | a0001c0002t0001g0235a0001c0023t0004g0121a0001c0050t0001g0277others(12): Show | 15 | HG00735.hp2 HG01074.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.654-4866dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109161980 | |||||
| chr12:109162062
|
T | C | 230 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(227): Show | 230 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.654-4799T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109162062 | ||||||
| chr12:109162069
|
C | T | 5 | a0001c0054t0001g0203a0001c0055t0001g0226a0001c0095t0001g0133others(2): Show | 5 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-4792C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109162069 | ||||||
| chr12:109162165
|
G | A | 1 | a0002c0020t0003g0273 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.654-4696G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109162165 | ||||||
| chr12:109162409
|
A | G | 237 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(234): Show | 237 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.654-4452A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109162409 | ||||||
| chr12:109162473
|
C | T | 4 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(1): Show | 4 | HG03139.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-4388C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109162473 | ||||||
| chr12:109162512
|
C | T | 2 | a0001c0069t0002g0204a0017c0123t0015g0058 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.654-4349C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109162512 | ||||||
| chr12:109162513
|
G | A | 1 | a0002c0006t0014g0080 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.654-4348G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109162513 | ||||||
| chr12:109162513
|
G | T | 4 | a0001c0016t0011g0274a0001c0124t0012g0197a0007c0057t0004g0207others(1): Show | 4 | HG02965.hp1 HG03540.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-4348G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109162513 | ||||||
| chr12:109162605
|
AG | A | 9 | a0001c0105t0004g0296a0001c0106t0001g0293a0001c0109t0002g0276others(6): Show | 9 | HG01168.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.654-4253delG | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109162605 | |||||
| chr12:109162644
|
C | G | 4 | a0001c0038t0001g0201a0002c0070t0005g0199a0007c0037t0004g0200others(1): Show | 4 | HG02145.hp2 HG02717.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-4217C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109162644 | ||||||
| chr12:109162756
|
A | C | 2 | a0001c0010t0001g0188a0001c0010t0009g0186 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.654-4105A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109162756 | ||||||
| chr12:109162770
|
A | G | 124 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(121): Show | 124 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.654-4091A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109162770 | ||||||
| chr12:109162794
|
C | T | 1 | a0038c0082t0002g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.654-4067C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109162794 | ||||||
| chr12:109162798
|
G | A | 2 | a0001c0010t0001g0188a0001c0010t0009g0186 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.654-4063G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109162798 | ||||||
| chr12:109163008
|
C | T | 3 | a0001c0003t0002g0077a0001c0003t0002g0097a0040c0115t0001g0258 | 3 | HG00438.hp1 NA18987.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.654-3853C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109163008 | ||||||
| chr12:109163009
|
C | T | 7 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0109t0002g0276others(4): Show | 7 | HG01074.hp1 HG01175.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.654-3852C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109163009 | ||||||
| chr12:109163075
|
C | T | 1 | a0001c0004t0017g0003 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.654-3786C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109163075 | ||||||
| chr12:109163162
|
T | C | 4 | a0001c0038t0001g0201a0002c0070t0005g0199a0007c0037t0004g0200others(1): Show | 4 | HG02145.hp2 HG02717.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-3699T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109163162 | ||||||
| chr12:109163204
|
C | T | 1 | a0024c0091t0002g0174 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.654-3657C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109163204 | ||||||
| chr12:109163244
|
A | G | 4 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(1): Show | 4 | HG03139.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-3617A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109163244 | ||||||
| chr12:109163592
|
G | A | 52 | a0001c0013t0001g0153a0001c0045t0002g0146a0003c0001t0001g0064others(49): Show | 52 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.654-3269G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109163592 | ||||||
| chr12:109163635
|
A | G | 118 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.654-3226A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109163635 | ||||||
| chr12:109163678
|
C | T | 1 | a0027c0065t0005g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.654-3183C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109163678 | ||||||
| chr12:109163684
|
C | G | 1 | a0040c0115t0001g0258 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.654-3177C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109163684 | ||||||
| chr12:109163794
|
T | C | 238 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.654-3067T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109163794 | ||||||
| chr12:109163810
|
C | T | 8 | a0001c0046t0002g0067a0001c0046t0002g0190a0001c0089t0002g0162others(5): Show | 8 | HG00544.hp2 HG00609.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.654-3051C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109163810 | ||||||
| chr12:109163955
|
A | G | 114 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.654-2906A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109163955 | ||||||
| chr12:109164055
|
T | C | 211 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.654-2806T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109164055 | ||||||
| chr12:109164162
|
T | C | 5 | a0001c0054t0001g0203a0001c0055t0001g0226a0001c0095t0001g0133others(2): Show | 5 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-2699T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109164162 | ||||||
| chr12:109164271
|
C | T | 1 | a0001c0003t0002g0104 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.654-2590C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109164271 | ||||||
| chr12:109164295
|
C | T | 1 | a0001c0048t0002g0281 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.654-2566C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109164295 | ||||||
| chr12:109164435
|
T | C | 2 | a0001c0010t0001g0188a0001c0010t0009g0186 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.654-2426T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109164435 | ||||||
| chr12:109164541
|
A | C | 1 | a0001c0018t0002g0049 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.654-2320A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109164541 | ||||||
| chr12:109164717
|
A | AT | 134 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.654-2126dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109164717 | |||||
| chr12:109164717
|
A | ATT | 69 | a0001c0002t0001g0114a0001c0003t0004g0300a0001c0013t0001g0153others(66): Show | 69 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.654-2127_654-2126d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109164717 | |||||
| chr12:109164717
|
A | T | 1 | a0017c0123t0015g0058 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.654-2144A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109164717 | ||||||
| chr12:109164717
|
AT | A | 6 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0032t0004g0292others(3): Show | 6 | HG01891.hp1 HG01943.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.654-2126delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109164717 | |||||
| chr12:109164822
|
ATTCTCCC others(9): Show |
A | 11 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0050t0001g0277others(8): Show | 11 | HG01074.hp1 HG01175.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.654-2035_654-2020d others(18): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109164822 | |||||
| chr12:109164880
|
G | A | 1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.654-1981G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109164880 | ||||||
| chr12:109164916
|
T | G | 6 | a0001c0054t0001g0203a0001c0055t0001g0226a0001c0095t0001g0133others(3): Show | 6 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.654-1945T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109164916 | ||||||
| chr12:109164918
|
T | C | 196 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.654-1943T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109164918 | ||||||
| chr12:109164931
|
C | A | 196 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.654-1930C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109164931 | ||||||
| chr12:109164959
|
CACAGGAG others(7): Show |
C | 2 | a0001c0012t0002g0262a0002c0086t0003g0260 | 2 | HG00423.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.654-1893_654-1880d others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109164959 | |||||
| chr12:109165075
|
C | T | 7 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0109t0002g0276others(4): Show | 7 | HG01074.hp1 HG01175.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.654-1786C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109165075 | ||||||
| chr12:109165224
|
T | C | 1 | a0002c0092t0010g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.654-1637T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109165224 | ||||||
| chr12:109165295
|
G | C | 14 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(11): Show | 14 | HG00423.hp1 HG00544.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.654-1566G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109165295 | ||||||
| chr12:109165346
|
C | A | 95 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.654-1515C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109165346 | ||||||
| chr12:109165667
|
T | A | 1 | a0001c0111t0001g0275 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.654-1194T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109165667 | ||||||
| chr12:109165689
|
A | T | 238 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.654-1172A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109165689 | ||||||
| chr12:109165765
|
G | A | 3 | a0001c0004t0017g0003a0007c0037t0004g0073a0026c0066t0015g0115 | 3 | HG02559.hp2 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.654-1096G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109165765 | ||||||
| chr12:109165820
|
T | C | 9 | a0001c0004t0017g0003a0001c0016t0009g0287a0001c0016t0009g0290others(6): Show | 9 | HG01081.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.654-1041T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109165820 | ||||||
| chr12:109165872
|
G | A | 1 | a0002c0097t0003g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.654-989G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109165872 | ||||||
| chr12:109165943
|
A | T | 11 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0050t0001g0277others(8): Show | 11 | HG01074.hp1 HG01175.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.654-918A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109165943 | ||||||
| chr12:109166126
|
C | T | 216 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.654-735C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166126 | ||||||
| chr12:109166250
|
A | G | 91 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(88): Show | 91 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.654-611A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166250 | ||||||
| chr12:109166320
|
C | G | 1 | a0003c0005t0002g0134 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.654-541C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166320 | ||||||
| chr12:109166373
|
C | A | 1 | a0001c0013t0001g0248 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.654-488C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166373 | ||||||
| chr12:109166412
|
G | T | 7 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0109t0002g0276others(4): Show | 7 | HG01074.hp1 HG01175.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.654-449G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166412 | ||||||
| chr12:109166430
|
G | A | 96 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.654-431G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166430 | ||||||
| chr12:109166480
|
G | A | 8 | a0001c0016t0011g0274a0001c0054t0001g0203a0001c0055t0001g0226others(5): Show | 8 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-381G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166480 | ||||||
| chr12:109166568
|
C | T | 4 | a0003c0001t0001g0140a0003c0001t0001g0141a0003c0001t0001g0142others(1): Show | 4 | NA18945.hp2 NA18993.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-293C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166568 | ||||||
| chr12:109166597
|
C | T | 1 | a0002c0006t0003g0194 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.654-264C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166597 | ||||||
| chr12:109166615
|
A | G | 238 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.654-246A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166615 | ||||||
| chr12:109166649
|
C | CA | 38 | a0001c0004t0002g0052a0001c0004t0007g0011a0001c0004t0007g0019others(35): Show | 38 | HG00597.hp1 HG01074.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.654-184dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109166649 | |||||
| chr12:109166649
|
C | CAAAAAA | 23 | a0001c0002t0001g0035a0001c0002t0001g0126a0001c0003t0002g0077others(20): Show | 23 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.654-189_654-184dup others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109166649 | |||||
| chr12:109166649
|
C | CAAAAAAA | 41 | a0001c0002t0001g0079a0001c0002t0001g0081a0001c0002t0001g0114others(38): Show | 41 | HG00558.hp1 HG00597.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.654-190_654-184dup others(7): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109166649 | |||||
| chr12:109166649
|
C | CAAAAAAA others(1): Show |
20 | a0001c0002t0001g0075a0001c0002t0001g0109a0001c0002t0001g0235others(17): Show | 20 | HG00423.hp2 HG00642.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.654-191_654-184dup others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109166649 | |||||
| chr12:109166649
|
C | CAAAAAAA others(3): Show |
1 | a0002c0024t0003g0302 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.654-193_654-184dup others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109166649 | |||||
| chr12:109166649
|
C | CAAAAAAA others(4): Show |
1 | a0001c0003t0002g0193 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.654-194_654-184dup others(11): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109166649 | |||||
| chr12:109166675
|
AAAC | A | 83 | a0001c0004t0017g0003a0001c0012t0002g0045a0001c0012t0002g0250others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.654-185_654-183del others(3): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166675 | ||||||
| chr12:109166676
|
AAC | A | 24 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0016t0009g0287others(21): Show | 24 | HG00408.hp2 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.654-184_654-183del others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166676 | ||||||
| chr12:109166677
|
AC | A | 12 | a0001c0058t0016g0187a0006c0026t0002g0156a0006c0026t0016g0066others(9): Show | 12 | HG00323.hp1 HG01167.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.654-182delC | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | 109166677 | |||||
| chr12:109166678
|
C | A | 107 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(104): Show | 107 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.654-183C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166678 | ||||||
| chr12:109166694
|
C | A | 242 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.654-167C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166694 | ||||||
| chr12:109166775
|
T | C | 1 | a0003c0005t0002g0245 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.654-86T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166775 | ||||||
| chr12:109166801
|
G | A | 1 | a0001c0011t0001g0157 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.654-60G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | 109166801 | ||||||
| chr12:109167088
|
T | A | 3 | a0001c0010t0001g0188a0001c0010t0009g0186a0009c0096t0009g0295 | 3 | HG02717.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.786+95T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167088 | ||||||
| chr12:109167089
|
C | G | 3 | a0001c0010t0001g0188a0001c0010t0009g0186a0009c0096t0009g0295 | 3 | HG02717.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.786+96C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167089 | ||||||
| chr12:109167106
|
G | T | 1 | a0001c0038t0001g0029 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.786+113G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167106 | ||||||
| chr12:109167212
|
A | G | 1 | a0002c0006t0003g0194 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.786+219A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167212 | ||||||
| chr12:109167347
|
G | A | 98 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.786+354G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167347 | ||||||
| chr12:109167411
|
G | A | 221 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.786+418G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167411 | ||||||
| chr12:109167453
|
G | C | 5 | a0001c0054t0001g0203a0001c0055t0001g0226a0001c0095t0001g0133others(2): Show | 5 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-443G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167453 | ||||||
| chr12:109167501
|
A | T | 4 | a0001c0038t0001g0201a0002c0070t0005g0199a0007c0037t0004g0200others(1): Show | 4 | HG02145.hp2 HG02717.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-395A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167501 | ||||||
| chr12:109167514
|
A | G | 5 | a0001c0016t0009g0287a0001c0016t0009g0290a0001c0016t0009g0305others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-382A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167514 | ||||||
| chr12:109167608
|
A | T | 2 | a0010c0042t0003g0209a0020c0052t0001g0210 | 2 | HG02698.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.787-288A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167608 | ||||||
| chr12:109167610
|
T | A | 2 | a0008c0015t0005g0171a0008c0015t0005g0172 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.787-286T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167610 | ||||||
| chr12:109167617
|
A | ATG | 3 | a0001c0034t0001g0211a0001c0034t0001g0212a0001c0048t0002g0281 | 3 | HG00099.hp1 HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.787-275_787-274dup others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167617 | |||||
| chr12:109167621
|
G | GATATATA others(20): Show |
1 | a0003c0001t0001g0158 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.787-275_787-274ins others(27): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167621 | ||||||
| chr12:109167621
|
G | GCATATAT others(7): Show |
2 | a0001c0064t0009g0184a0002c0118t0005g0231 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.787-275_787-274ins others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167621 | ||||||
| chr12:109167621
|
G | GCATATAT others(11): Show |
1 | a0001c0039t0004g0116 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.787-275_787-274ins others(18): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167621 | ||||||
| chr12:109167621
|
G | GCATATAT others(15): Show |
1 | a0001c0074t0004g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.787-275_787-274ins others(22): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167621 | ||||||
| chr12:109167621
|
G | GTA | 22 | a0001c0002t0001g0098a0001c0002t0001g0109a0001c0002t0001g0191others(19): Show | 22 | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.787-243_787-242dup others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATA | 26 | a0001c0003t0004g0300a0001c0011t0001g0008a0001c0016t0011g0274others(23): Show | 26 | HG00323.hp1 HG00323.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.787-245_787-242dup others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATA | 21 | a0001c0002t0001g0283a0001c0022t0004g0004a0001c0022t0004g0005others(18): Show | 21 | HG00642.hp2 HG00735.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.787-247_787-242dup others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(1): Show |
11 | a0001c0002t0001g0235a0001c0002t0021g0243a0001c0060t0002g0272others(8): Show | 11 | HG02027.hp2 HG02074.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-249_787-242dup others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(3): Show |
7 | a0001c0003t0002g0078a0002c0017t0024g0044a0002c0021t0006g0239others(4): Show | 7 | HG00621.hp1 HG02896.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.787-251_787-242dup others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(5): Show |
5 | a0001c0045t0002g0146a0003c0001t0001g0132a0011c0027t0004g0150others(2): Show | 5 | HG01168.hp2 HG01261.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-253_787-242dup others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(7): Show |
12 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0013t0001g0256others(9): Show | 12 | HG00280.hp2 HG00438.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.787-255_787-242dup others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(9): Show |
6 | a0001c0111t0001g0275a0002c0036t0003g0161a0003c0005t0002g0246others(3): Show | 6 | HG00408.hp2 HG01175.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-257_787-242dup others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(11): Show |
26 | a0001c0012t0002g0045a0001c0012t0002g0251a0001c0012t0002g0259others(23): Show | 26 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.787-259_787-242dup others(18): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(13): Show |
9 | a0001c0046t0002g0067a0001c0050t0001g0277a0002c0021t0003g0252others(6): Show | 9 | HG01074.hp1 HG03516.hp1 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.787-261_787-242dup others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(15): Show |
12 | a0001c0013t0001g0153a0001c0013t0001g0237a0002c0028t0003g0228others(9): Show | 12 | HG00621.hp2 HG01069.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.787-263_787-242dup others(22): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(17): Show |
6 | a0002c0086t0003g0260a0003c0001t0001g0137a0003c0005t0002g0060others(3): Show | 6 | HG00609.hp2 HG00639.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-265_787-242dup others(24): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(19): Show |
9 | a0001c0089t0002g0162a0003c0001t0001g0136a0003c0001t0001g0149others(6): Show | 9 | HG02040.hp1 HG02056.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.787-267_787-242dup others(26): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(21): Show |
5 | a0003c0001t0001g0265a0003c0005t0002g0059a0003c0083t0001g0151others(2): Show | 5 | HG00735.hp1 HG01109.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-269_787-242dup others(28): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(23): Show |
5 | a0002c0020t0003g0273a0003c0001t0004g0266a0003c0001t0008g0128others(2): Show | 5 | HG02738.hp2 HG03017.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-271_787-242dup others(30): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(25): Show |
1 | a0005c0009t0006g0177 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.787-273_787-242dup others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(27): Show |
3 | a0003c0001t0001g0143a0003c0001t0001g0298a0005c0009t0006g0148 | 3 | HG00741.hp2 NA18961.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.787-242_787-241ins others(34): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTATATAT others(29): Show |
2 | a0001c0124t0012g0197a0003c0001t0001g0297 | 2 | NA19011.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.787-242_787-241ins others(36): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTGTATAT others(7): Show |
1 | a0002c0053t0005g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.787-274_787-273ins others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTGTATAT others(15): Show |
1 | a0016c0047t0002g0175 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.787-274_787-273ins others(22): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
G | GTGTATAT others(19): Show |
1 | a0016c0047t0002g0176 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.787-274_787-273ins others(26): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
GTA | G | 5 | a0001c0002t0008g0306a0001c0004t0017g0003a0001c0010t0001g0188others(2): Show | 5 | HG01255.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-243_787-242del others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
GTATATAT others(1): Show |
G | 3 | a0013c0033t0002g0185a0013c0033t0002g0189a0027c0065t0005g0225 | 3 | HG01081.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.787-249_787-242del others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
GTATATAT others(3): Show |
G | 3 | a0001c0038t0001g0029a0002c0028t0003g0160a0014c0079t0004g0180 | 3 | HG00609.hp1 HG01433.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.787-251_787-242del others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
GTATATAT others(9): Show |
G | 2 | a0001c0069t0002g0204a0017c0123t0015g0058 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.787-257_787-242del others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167621
|
GTATATAT others(11): Show |
G | 6 | a0001c0105t0004g0296a0001c0106t0001g0293a0002c0006t0005g0294others(3): Show | 6 | HG01891.hp2 HG02809.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-259_787-242del others(18): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167621 | |||||
| chr12:109167643
|
A | ATATATAT others(9): Show |
1 | a0036c0094t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.787-242_787-241ins others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167643 | |||||
| chr12:109167643
|
A | ATATATAT others(7): Show |
2 | a0001c0054t0001g0203a0001c0095t0001g0133 | 2 | HG01943.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.787-242_787-241ins others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167643 | |||||
| chr12:109167643
|
A | ATATATAT others(5): Show |
1 | a0001c0055t0001g0226 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.787-251_787-240dup others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | 109167643 | |||||
| chr12:109167643
|
A | T | 1 | a0002c0053t0005g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.787-253A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167643 | ||||||
| chr12:109167654
|
T | TATATATA others(6): Show |
1 | a0001c0016t0009g0290 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.787-242_787-241ins others(13): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167654 | ||||||
| chr12:109167654
|
T | TATATATA others(14): Show |
1 | a0001c0050t0001g0278 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.787-242_787-241ins others(21): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167654 | ||||||
| chr12:109167654
|
T | TATATATA others(16): Show |
1 | a0001c0012t0002g0250 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.787-242_787-241ins others(23): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167654 | ||||||
| chr12:109167655
|
T | A | 1 | a0023c0099t0001g0084 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.787-241T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | chr12 | 109167655 | ||||||
| chr12:109168078
|
G | A | 1 | a0001c0004t0017g0003 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.925+44G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109168078 | ||||||
| chr12:109168087
|
C | T | 1 | a0014c0077t0004g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.925+53C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109168087 | ||||||
| chr12:109168093
|
C | T | 190 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.925+59C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109168093 | ||||||
| chr12:109168191
|
T | C | 242 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.925+157T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109168191 | ||||||
| chr12:109168290
|
C | G | 4 | a0001c0038t0001g0201a0002c0070t0005g0199a0007c0037t0004g0200others(1): Show | 4 | HG02145.hp2 HG02717.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+256C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109168290 | ||||||
| chr12:109168582
|
A | G | 5 | a0001c0054t0001g0203a0001c0055t0001g0226a0001c0095t0001g0133others(2): Show | 5 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+548A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109168582 | ||||||
| chr12:109168658
|
A | T | 95 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.925+624A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109168658 | ||||||
| chr12:109168692
|
C | T | 1 | a0001c0038t0001g0029 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.925+658C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109168692 | ||||||
| chr12:109168810
|
A | C | 91 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(88): Show | 91 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.925+776A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109168810 | ||||||
| chr12:109168819
|
C | G | 1 | a0016c0047t0002g0176 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.925+785C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109168819 | ||||||
| chr12:109168823
|
A | G | 91 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(88): Show | 91 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.925+789A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109168823 | ||||||
| chr12:109168848
|
A | G | 18 | a0001c0004t0017g0003a0001c0016t0009g0287a0001c0016t0009g0290others(15): Show | 18 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.925+814A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109168848 | ||||||
| chr12:109168942
|
T | G | 1 | a0001c0002t0001g0283 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.925+908T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109168942 | ||||||
| chr12:109169002
|
G | A | 1 | a0001c0049t0004g0088 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.925+968G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169002 | ||||||
| chr12:109169138
|
G | A | 2 | a0006c0113t0004g0031a0015c0114t0004g0009 | 2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.925+1104G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169138 | ||||||
| chr12:109169142
|
C | CAAA | 203 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0081others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.925+1124_925+1126d others(5): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | 109169142 | |||||
| chr12:109169142
|
C | CAAAA | 15 | a0001c0002t0001g0191a0001c0016t0011g0274a0001c0054t0001g0203others(12): Show | 15 | HG00597.hp2 HG01943.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.925+1123_925+1126d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | 109169142 | |||||
| chr12:109169142
|
CA | C | 42 | a0001c0038t0001g0201a0002c0007t0006g0017a0002c0070t0005g0199others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.925+1126delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | 109169142 | |||||
| chr12:109169246
|
A | G | 221 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.925+1212A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169246 | ||||||
| chr12:109169446
|
T | C | 201 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.925+1412T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169446 | ||||||
| chr12:109169502
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.925+1468A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169502 | ||||||
| chr12:109169527
|
T | C | 203 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.925+1493T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169527 | ||||||
| chr12:109169590
|
G | A | 1 | a0002c0043t0003g0012 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.925+1556G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169590 | ||||||
| chr12:109169614
|
G | C | 3 | a0001c0004t0002g0054a0001c0011t0001g0056a0002c0007t0003g0055 | 3 | HG01884.hp2 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.925+1580G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169614 | ||||||
| chr12:109169656
|
T | C | 1 | a0001c0046t0002g0190 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.925+1622T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169656 | ||||||
| chr12:109169704
|
C | T | 29 | a0001c0004t0017g0003a0001c0016t0009g0287a0001c0016t0009g0290others(26): Show | 29 | HG00323.hp1 HG01081.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.925+1670C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169704 | ||||||
| chr12:109169746
|
G | T | 98 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.925+1712G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169746 | ||||||
| chr12:109169767
|
T | C | 1 | a0007c0057t0004g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.925+1733T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169767 | ||||||
| chr12:109169863
|
G | A | 1 | a0005c0009t0003g0164 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.925+1829G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169863 | ||||||
| chr12:109169917
|
G | A | 127 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0012t0002g0045others(124): Show | 127 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.925+1883G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169917 | ||||||
| chr12:109169938
|
T | C | 2 | a0001c0010t0001g0188a0001c0010t0009g0186 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.926-1867T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169938 | ||||||
| chr12:109169988
|
A | T | 1 | a0012c0035t0004g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.926-1817A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109169988 | ||||||
| chr12:109170100
|
TTTTG | T | 20 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(17): Show | 20 | HG00323.hp1 HG01109.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.926-1690_926-1687d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | 109170100 | |||||
| chr12:109170212
|
G | A | 2 | a0001c0010t0001g0188a0001c0010t0009g0186 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.926-1593G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170212 | ||||||
| chr12:109170287
|
A | C | 1 | a0033c0063t0010g0117 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.926-1518A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170287 | ||||||
| chr12:109170326
|
A | G | 3 | a0001c0039t0004g0116a0001c0064t0009g0184a0001c0074t0004g0229 | 3 | HG01891.hp1 HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.926-1479A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170326 | ||||||
| chr12:109170480
|
C | T | 3 | a0001c0039t0004g0116a0001c0064t0009g0184a0001c0074t0004g0229 | 3 | HG01891.hp1 HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.926-1325C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170480 | ||||||
| chr12:109170657
|
G | A | 1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.926-1148G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170657 | ||||||
| chr12:109170660
|
A | G | 1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.926-1145A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170660 | ||||||
| chr12:109170684
|
C | T | 3 | a0001c0039t0004g0116a0001c0064t0009g0184a0001c0074t0004g0229 | 3 | HG01891.hp1 HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.926-1121C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170684 | ||||||
| chr12:109170710
|
G | C | 41 | a0001c0016t0011g0274a0001c0039t0004g0116a0001c0050t0001g0277others(38): Show | 41 | HG00323.hp1 HG01074.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.926-1095G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170710 | ||||||
| chr12:109170785
|
TTG | T | 128 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.926-1012_926-1011d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | 109170785 | |||||
| chr12:109170793
|
G | T | 3 | a0006c0113t0004g0031a0015c0114t0004g0009a0035c0076t0010g0267 | 3 | HG03098.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.926-1012G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170793 | ||||||
| chr12:109170793
|
GT | G | 138 | a0001c0004t0002g0054a0001c0004t0017g0003a0001c0010t0001g0188others(135): Show | 138 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.926-1001delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | 109170793 | |||||
| chr12:109170795
|
T | G | 8 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0069t0002g0204others(5): Show | 8 | HG01074.hp1 HG01175.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-1010T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170795 | ||||||
| chr12:109170798
|
T | A | 2 | a0006c0113t0004g0031a0015c0114t0004g0009 | 2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.926-1007T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170798 | ||||||
| chr12:109170824
|
T | G | 241 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.926-981T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170824 | ||||||
| chr12:109170844
|
G | C | 133 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.926-961G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170844 | ||||||
| chr12:109170913
|
T | C | 1 | a0001c0039t0004g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.926-892T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109170913 | ||||||
| chr12:109171013
|
A | AT | 76 | a0001c0002t0001g0091a0001c0002t0001g0282a0001c0003t0002g0103others(73): Show | 76 | HG00323.hp1 HG00438.hp2 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.926-771dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | 109171013 | |||||
| chr12:109171013
|
A | ATT | 61 | a0001c0002t0001g0035a0001c0002t0001g0079a0001c0002t0001g0081others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.926-772_926-771dup others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | 109171013 | |||||
| chr12:109171013
|
A | ATTT | 9 | a0001c0002t0001g0075a0001c0002t0001g0114a0001c0002t0001g0235others(6): Show | 9 | HG00423.hp2 HG00673.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.926-773_926-771dup others(3): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | 109171013 | |||||
| chr12:109171223
|
C | T | 1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.926-582C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109171223 | ||||||
| chr12:109171264
|
C | T | 1 | a0001c0003t0002g0244 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.926-541C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109171264 | ||||||
| chr12:109171301
|
A | G | 2 | a0006c0113t0004g0031a0015c0114t0004g0009 | 2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.926-504A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109171301 | ||||||
| chr12:109171353
|
C | CT | 33 | a0001c0016t0011g0274a0001c0039t0004g0116a0001c0054t0001g0203others(30): Show | 33 | HG00323.hp1 HG01109.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.926-440dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | 109171353 | |||||
| chr12:109171381
|
G | A | 2 | a0004c0008t0001g0218a0004c0008t0008g0219 | 2 | NA18981.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.926-424G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109171381 | ||||||
| chr12:109171489
|
A | G | 4 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(1): Show | 4 | HG03139.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-316A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109171489 | ||||||
| chr12:109171540
|
G | T | 1 | a0003c0001t0001g0154 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.926-265G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109171540 | ||||||
| chr12:109171563
|
C | T | 1 | a0038c0082t0002g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.926-242C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109171563 | ||||||
| chr12:109171601
|
C | T | 104 | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0009g0186others(101): Show | 104 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.926-204C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109171601 | ||||||
| chr12:109171714
|
C | A | 10 | a0003c0001t0001g0087a0003c0001t0001g0149a0003c0005t0002g0129others(7): Show | 10 | HG00735.hp1 HG01109.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.926-91C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109171714 | ||||||
| chr12:109171723
|
T | C | 86 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(83): Show | 86 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.926-82T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109171723 | ||||||
| chr12:109171746
|
T | C | 1 | a0014c0077t0004g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.926-59T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | chr12 | 109171746 | ||||||
| chr12:109172092
|
A | T | 99 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1035+178A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 5/52 | chr12 | 109172092 | ||||||
| chr12:109172166
|
C | T | 1 | a0001c0003t0002g0068 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1036-109C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 5/52 | chr12 | 109172166 | ||||||
| chr12:109172201
|
C | T | 7 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0022t0004g0004others(4): Show | 7 | HG02717.hp1 HG02723.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036-74C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 5/52 | chr12 | 109172201 | ||||||
| chr12:109172997
|
C | T | 1 | a0006c0026t0016g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1117+641C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109172997 | ||||||
| chr12:109172999
|
G | A | 1 | a0039c0080t0010g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1117+643G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109172999 | ||||||
| chr12:109173333
|
T | C | 2 | a0001c0002t0021g0243a0023c0099t0001g0084 | 2 | NA18950.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1118-799T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109173333 | ||||||
| chr12:109173370
|
G | A | 1 | a0001c0046t0002g0190 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1118-762G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109173370 | ||||||
| chr12:109173462
|
C | T | 1 | a0004c0112t0001g0119 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1118-670C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109173462 | ||||||
| chr12:109173668
|
C | T | 5 | a0001c0004t0017g0003a0001c0016t0011g0274a0001c0124t0012g0197others(2): Show | 5 | HG02965.hp1 HG03130.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1118-464C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109173668 | ||||||
| chr12:109173783
|
A | G | 4 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(1): Show | 4 | HG03139.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1118-349A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109173783 | ||||||
| chr12:109173811
|
T | G | 2 | a0006c0113t0004g0031a0015c0114t0004g0009 | 2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1118-321T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109173811 | ||||||
| chr12:109173915
|
A | G | 101 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.1118-217A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109173915 | ||||||
| chr12:109174053
|
G | A | 1 | a0018c0051t0023g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1118-79G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109174053 | ||||||
| chr12:109174096
|
C | T | 20 | a0001c0058t0016g0187a0006c0026t0002g0155a0006c0026t0002g0156others(17): Show | 20 | HG00323.hp1 HG01109.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1118-36C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109174096 | ||||||
| chr12:109174097
|
G | A | 1 | a0014c0079t0004g0180 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1118-35G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109174097 | ||||||
| chr12:109174105
|
C | T | 2 | a0001c0069t0002g0204a0017c0123t0015g0058 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1118-27C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109174105 | ||||||
| chr12:109174121
|
C | G | 5 | a0001c0054t0001g0203a0001c0055t0001g0226a0001c0095t0001g0133others(2): Show | 5 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1118-11C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 6/52 | chr12 | 109174121 | ||||||
| chr12:109174535
|
C | G | 211 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1216+305C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | chr12 | 109174535 | ||||||
| chr12:109174548
|
G | GA | 107 | a0001c0004t0017g0003a0001c0012t0002g0045a0001c0012t0002g0250others(104): Show | 107 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1216+334dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | INFO_REALIGN_3_PRIME | chr12 | 109174548 | |||||
| chr12:109174549
|
A | G | 9 | a0001c0048t0004g0307a0001c0049t0001g0289a0001c0060t0002g0272others(6): Show | 9 | HG02109.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1216+319A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | chr12 | 109174549 | ||||||
| chr12:109174706
|
T | TA | 94 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1216+490dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | INFO_REALIGN_3_PRIME | chr12 | 109174706 | |||||
| chr12:109174721
|
T | A | 6 | a0001c0002t0001g0235a0001c0002t0001g0241a0001c0002t0001g0242others(3): Show | 6 | HG02027.hp2 NA18950.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1216+491T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | chr12 | 109174721 | ||||||
| chr12:109174756
|
A | G | 106 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1216+526A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | chr12 | 109174756 | ||||||
| chr12:109174856
|
C | T | 101 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.1216+626C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | chr12 | 109174856 | ||||||
| chr12:109175222
|
G | GT | 7 | a0001c0029t0002g0096a0002c0007t0003g0037a0002c0007t0003g0041others(4): Show | 7 | HG00673.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1217-700dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | INFO_REALIGN_3_PRIME | chr12 | 109175222 | |||||
| chr12:109175222
|
GT | G | 7 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0109t0002g0276others(4): Show | 7 | HG01074.hp1 HG01109.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1217-700delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | INFO_REALIGN_3_PRIME | chr12 | 109175222 | |||||
| chr12:109175230
|
T | C | 1 | a0012c0035t0004g0082 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1217-701T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | chr12 | 109175230 | ||||||
| chr12:109175297
|
A | T | 1 | a0002c0036t0003g0161 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1217-634A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | chr12 | 109175297 | ||||||
| chr12:109175421
|
T | C | 23 | a0001c0058t0016g0187a0006c0026t0002g0155a0006c0026t0002g0156others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.1217-510T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | chr12 | 109175421 | ||||||
| chr12:109175434
|
G | A | 1 | a0002c0020t0003g0273 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1217-497G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | chr12 | 109175434 | ||||||
| chr12:109175541
|
G | C | 2 | a0001c0002t0001g0282a0001c0003t0004g0300 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1217-390G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | chr12 | 109175541 | ||||||
| chr12:109175677
|
C | A | 2 | a0001c0069t0002g0204a0017c0123t0015g0058 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1217-254C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | chr12 | 109175677 | ||||||
| chr12:109176134
|
G | A | 1 | a0027c0065t0005g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1327-19G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 8/52 | chr12 | 109176134 | ||||||
| chr12:109176410
|
C | T | 1 | a0002c0118t0005g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1437+147C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109176410 | ||||||
| chr12:109176413
|
G | A | 1 | a0001c0107t0012g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1437+150G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109176413 | ||||||
| chr12:109176478
|
A | G | 2 | a0001c0011t0001g0013a0005c0056t0003g0053 | 2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1437+215A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109176478 | ||||||
| chr12:109176488
|
A | G | 20 | a0001c0058t0016g0187a0006c0026t0002g0155a0006c0026t0002g0156others(17): Show | 20 | HG00323.hp1 HG01109.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1437+225A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109176488 | ||||||
| chr12:109176757
|
C | T | 82 | a0001c0004t0017g0003a0001c0012t0002g0045a0001c0012t0002g0250others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1437+494C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109176757 | ||||||
| chr12:109176778
|
A | G | 82 | a0001c0004t0017g0003a0001c0012t0002g0045a0001c0012t0002g0250others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1437+515A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109176778 | ||||||
| chr12:109176863
|
C | T | 1 | a0002c0092t0010g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1437+600C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109176863 | ||||||
| chr12:109176903
|
C | T | 95 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1437+640C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109176903 | ||||||
| chr12:109176908
|
C | T | 1 | a0002c0014t0003g0015 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1437+645C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109176908 | ||||||
| chr12:109176909
|
G | A | 6 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0109t0002g0276others(3): Show | 6 | HG01074.hp1 HG01175.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1437+646G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109176909 | ||||||
| chr12:109177322
|
T | A | 2 | a0006c0026t0002g0155a0006c0026t0002g0156 | 2 | HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1437+1059T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109177322 | ||||||
| chr12:109177600
|
A | G | 2 | a0001c0069t0002g0204a0017c0123t0015g0058 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1437+1337A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109177600 | ||||||
| chr12:109177632
|
C | T | 1 | a0008c0015t0005g0168 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1437+1369C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109177632 | ||||||
| chr12:109177721
|
A | G | 1 | a0002c0036t0006g0223 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1438-1367A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109177721 | ||||||
| chr12:109177729
|
C | G | 1 | a0003c0001t0001g0138 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1438-1359C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109177729 | ||||||
| chr12:109177934
|
T | C | 77 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(74): Show | 77 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1438-1154T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109177934 | ||||||
| chr12:109178178
|
C | T | 229 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1438-910C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109178178 | ||||||
| chr12:109178274
|
T | A | 2 | a0001c0046t0002g0067a0001c0046t0002g0190 | 2 | NA18959.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1438-814T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109178274 | ||||||
| chr12:109178373
|
C | T | 1 | a0002c0024t0003g0302 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1438-715C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109178373 | ||||||
| chr12:109178418
|
T | G | 3 | a0001c0002t0001g0079a0001c0002t0001g0091a0001c0003t0002g0193 | 3 | HG00741.hp1 HG01070.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1438-670T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109178418 | ||||||
| chr12:109178504
|
T | G | 2 | a0001c0069t0002g0204a0017c0123t0015g0058 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1438-584T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109178504 | ||||||
| chr12:109178594
|
G | A | 2 | a0001c0002t0001g0126a0001c0108t0001g0010 | 2 | HG02258.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1438-494G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109178594 | ||||||
| chr12:109178725
|
A | G | 8 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0069t0002g0204others(5): Show | 8 | HG01074.hp1 HG01175.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1438-363A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109178725 | ||||||
| chr12:109178803
|
C | T | 1 | a0003c0001t0001g0141 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1438-285C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109178803 | ||||||
| chr12:109178898
|
C | T | 5 | a0001c0054t0001g0203a0001c0055t0001g0226a0001c0095t0001g0133others(2): Show | 5 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1438-190C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109178898 | ||||||
| chr12:109178943
|
C | T | 1 | a0007c0030t0002g0110 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1438-145C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109178943 | ||||||
| chr12:109178997
|
G | A | 1 | a0002c0117t0003g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1438-91G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109178997 | ||||||
| chr12:109179051
|
C | T | 6 | a0001c0002t0001g0235a0001c0002t0001g0241a0001c0002t0001g0242others(3): Show | 6 | HG02027.hp2 NA18950.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1438-37C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109179051 | ||||||
| chr12:109179083
|
G | A | 1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | splice_region_variant&intron_variant | LOW | c.1438-5G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 9/52 | chr12 | 109179083 | ||||||
| chr12:109179415
|
T | A | 1 | a0027c0065t0005g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1647+118T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 10/52 | chr12 | 109179415 | ||||||
| chr12:109179643
|
T | C | 1 | a0001c0011t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1648-274T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 10/52 | chr12 | 109179643 | ||||||
| chr12:109179657
|
T | A | 6 | a0001c0054t0001g0203a0001c0055t0001g0226a0001c0095t0001g0133others(3): Show | 6 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1648-260T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 10/52 | chr12 | 109179657 | ||||||
| chr12:109179738
|
G | A | 3 | a0001c0002t0001g0126a0001c0108t0001g0010a0001c0109t0002g0276 | 3 | HG02258.hp2 HG03239.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1648-179G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 10/52 | chr12 | 109179738 | ||||||
| chr12:109179842
|
G | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1648-75G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 10/52 | chr12 | 109179842 | ||||||
| chr12:109179867
|
C | T | 1 | a0003c0001t0001g0138 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1648-50C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 10/52 | chr12 | 109179867 | ||||||
| chr12:109180158
|
G | C | 8 | a0001c0105t0004g0296a0001c0106t0001g0293a0002c0006t0005g0294others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1818+71G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109180158 | ||||||
| chr12:109180165
|
C | T | 5 | a0001c0054t0001g0203a0001c0055t0001g0226a0001c0095t0001g0133others(2): Show | 5 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1818+78C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109180165 | ||||||
| chr12:109180246
|
C | T | 1 | a0001c0124t0012g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1818+159C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109180246 | ||||||
| chr12:109180295
|
A | G | 81 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1818+208A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109180295 | ||||||
| chr12:109180446
|
A | G | 5 | a0001c0049t0001g0289a0001c0062t0019g0288a0001c0098t0001g0286others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1818+359A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109180446 | ||||||
| chr12:109180699
|
G | A | 2 | a0001c0004t0002g0050a0001c0004t0002g0052 | 2 | HG00597.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1818+612G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109180699 | ||||||
| chr12:109180786
|
G | T | 5 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(2): Show | 5 | HG00323.hp1 HG02523.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.1818+699G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109180786 | ||||||
| chr12:109180945
|
G | A | 8 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0069t0002g0204others(5): Show | 8 | HG01074.hp1 HG01175.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1818+858G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109180945 | ||||||
| chr12:109181136
|
C | T | 5 | a0001c0054t0001g0203a0001c0055t0001g0226a0001c0095t0001g0133others(2): Show | 5 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1818+1049C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109181136 | ||||||
| chr12:109181139
|
G | A | 2 | a0001c0003t0002g0094a0002c0014t0003g0083 | 2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1818+1052G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109181139 | ||||||
| chr12:109181229
|
C | CT | 44 | a0001c0002t0001g0075a0001c0010t0001g0188a0001c0010t0009g0186others(41): Show | 44 | HG00323.hp1 HG01109.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.1818+1158dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | INFO_REALIGN_3_PRIME | chr12 | 109181229 | |||||
| chr12:109181234
|
T | C | 4 | a0003c0001t0001g0145a0005c0009t0003g0061a0005c0009t0003g0144others(1): Show | 4 | NA18942.hp1 NA18960.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1818+1147T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109181234 | ||||||
| chr12:109181357
|
A | G | 1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1818+1270A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109181357 | ||||||
| chr12:109181371
|
G | A | 1 | a0003c0005t0002g0264 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1818+1284G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109181371 | ||||||
| chr12:109181537
|
T | C | 2 | a0001c0002t0001g0079a0001c0002t0001g0091 | 2 | HG00741.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.1818+1450T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109181537 | ||||||
| chr12:109181550
|
A | G | 15 | a0004c0008t0001g0198a0004c0008t0001g0218a0004c0008t0001g0221others(12): Show | 15 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1818+1463A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109181550 | ||||||
| chr12:109181638
|
G | A | 2 | a0006c0121t0004g0170a0006c0122t0004g0167 | 2 | HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1818+1551G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109181638 | ||||||
| chr12:109181840
|
C | CT | 16 | a0001c0022t0004g0004a0001c0050t0001g0277a0001c0050t0001g0278others(13): Show | 16 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1818+1775dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | INFO_REALIGN_3_PRIME | chr12 | 109181840 | |||||
| chr12:109181840
|
C | CTT | 16 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0022t0004g0005others(13): Show | 16 | HG01515.hp1 HG01943.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.1818+1774_1818+177 others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | INFO_REALIGN_3_PRIME | chr12 | 109181840 | |||||
| chr12:109181840
|
C | CTTT | 189 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0081others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1818+1773_1818+177 others(7): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | INFO_REALIGN_3_PRIME | chr12 | 109181840 | |||||
| chr12:109181840
|
C | CTTTT | 8 | a0001c0002t0001g0126a0001c0002t0001g0235a0001c0003t0002g0103others(5): Show | 8 | HG01109.hp1 HG01175.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1818+1772_1818+177 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | INFO_REALIGN_3_PRIME | chr12 | 109181840 | |||||
| chr12:109181864
|
A | G | 23 | a0001c0058t0016g0187a0006c0026t0002g0155a0006c0026t0002g0156others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.1818+1777A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109181864 | ||||||
| chr12:109181989
|
G | A | 1 | a0001c0002t0008g0306 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1818+1902G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109181989 | ||||||
| chr12:109181997
|
C | T | 14 | a0001c0058t0016g0187a0006c0031t0004g0002a0006c0031t0004g0206others(11): Show | 14 | HG01109.hp2 HG01167.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1818+1910C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109181997 | ||||||
| chr12:109182111
|
G | A | 1 | a0006c0113t0004g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1818+2024G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109182111 | ||||||
| chr12:109182133
|
G | A | 5 | a0001c0054t0001g0203a0001c0055t0001g0226a0001c0095t0001g0133others(2): Show | 5 | HG01943.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1818+2046G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109182133 | ||||||
| chr12:109182243
|
A | T | 204 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1818+2156A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109182243 | ||||||
| chr12:109182253
|
T | G | 2 | a0006c0113t0004g0031a0015c0114t0004g0009 | 2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1818+2166T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109182253 | ||||||
| chr12:109182359
|
A | C | 3 | a0001c0002t0001g0282a0001c0003t0004g0300a0018c0051t0023g0279 | 3 | HG02615.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1818+2272A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109182359 | ||||||
| chr12:109182470
|
C | T | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1818+2383C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109182470 | ||||||
| chr12:109182641
|
G | A | 8 | a0006c0121t0004g0170a0006c0122t0004g0167a0008c0015t0005g0057others(5): Show | 8 | HG02280.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1818+2554G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109182641 | ||||||
| chr12:109182647
|
G | A | 2 | a0001c0069t0002g0204a0017c0123t0015g0058 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1818+2560G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109182647 | ||||||
| chr12:109182690
|
G | A | 1 | a0001c0038t0001g0029 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1818+2603G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109182690 | ||||||
| chr12:109182705
|
G | A | 3 | a0001c0003t0002g0104a0001c0069t0002g0204a0017c0123t0015g0058 | 3 | HG01884.hp1 HG03669.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1818+2618G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109182705 | ||||||
| chr12:109183646
|
T | G | 1 | a0003c0001t0001g0154 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1819-1933T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109183646 | ||||||
| chr12:109183778
|
C | G | 1 | a0001c0003t0002g0078 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1819-1801C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109183778 | ||||||
| chr12:109183804
|
T | C | 3 | a0001c0023t0001g0122a0001c0023t0004g0121a0002c0097t0003g0124 | 3 | HG00735.hp2 HG01258.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1819-1775T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109183804 | ||||||
| chr12:109183975
|
G | A | 1 | a0001c0011t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1819-1604G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109183975 | ||||||
| chr12:109183982
|
A | G | 1 | a0003c0005t0002g0264 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1819-1597A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109183982 | ||||||
| chr12:109184119
|
C | G | 96 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1819-1460C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109184119 | ||||||
| chr12:109184241
|
C | T | 5 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(2): Show | 5 | HG03139.hp1 HG03579.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1819-1338C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109184241 | ||||||
| chr12:109184362
|
A | G | 1 | a0001c0029t0002g0096 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1819-1217A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109184362 | ||||||
| chr12:109184400
|
A | G | 1 | a0014c0077t0004g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1819-1179A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109184400 | ||||||
| chr12:109184435
|
C | G | 254 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1819-1144C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109184435 | ||||||
| chr12:109184501
|
C | A | 1 | a0001c0074t0004g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1819-1078C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109184501 | ||||||
| chr12:109184558
|
A | G | 3 | a0001c0002t0001g0085a0001c0003t0002g0068a0007c0101t0002g0086 | 3 | HG00099.hp2 HG02145.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1819-1021A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109184558 | ||||||
| chr12:109184672
|
G | T | 1 | a0001c0038t0001g0029 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1819-907G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109184672 | ||||||
| chr12:109184706
|
A | AT | 25 | a0001c0058t0016g0187a0001c0087t0001g0236a0004c0008t0001g0198others(22): Show | 25 | HG00323.hp1 HG00438.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1819-856dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | INFO_REALIGN_3_PRIME | chr12 | 109184706 | |||||
| chr12:109184738
|
G | A | 22 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(19): Show | 22 | HG00323.hp1 HG01109.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.1819-841G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109184738 | ||||||
| chr12:109184949
|
C | T | 1 | a0001c0049t0001g0289 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1819-630C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109184949 | ||||||
| chr12:109184992
|
A | C | 6 | a0001c0004t0002g0054a0001c0011t0001g0056a0001c0039t0004g0039others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1819-587A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109184992 | ||||||
| chr12:109185170
|
A | G | 7 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0109t0002g0276others(4): Show | 7 | HG01074.hp1 HG01175.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1819-409A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109185170 | ||||||
| chr12:109185281
|
C | T | 23 | a0001c0058t0016g0187a0006c0026t0002g0155a0006c0026t0002g0156others(20): Show | 23 | HG00323.hp1 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.1819-298C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109185281 | ||||||
| chr12:109185289
|
G | A | 13 | a0003c0001t0001g0132a0003c0001t0001g0136a0003c0001t0001g0137others(10): Show | 13 | HG00609.hp2 HG00673.hp2 NA18945.hp2 others(10): Show |
intron_variant | MODIFIER | c.1819-290G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109185289 | ||||||
| chr12:109185363
|
A | G | 3 | a0001c0002t0001g0126a0001c0023t0001g0089a0001c0108t0001g0010 | 3 | HG01123.hp2 HG02258.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1819-216A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109185363 | ||||||
| chr12:109185531
|
G | A | 8 | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0069t0002g0204others(5): Show | 8 | HG01074.hp1 HG01175.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1819-48G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | chr12 | 109185531 | ||||||
| chr12:109185795
|
G | C | 1 | a0014c0077t0004g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1980+55G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | chr12 | 109185795 | ||||||
| chr12:109186143
|
C | G | 1 | a0014c0077t0004g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1980+403C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | chr12 | 109186143 | ||||||
| chr12:109186177
|
C | T | 2 | a0001c0069t0002g0204a0017c0123t0015g0058 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1980+437C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | chr12 | 109186177 | ||||||
| chr12:109186491
|
T | C | 204 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1980+751T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | chr12 | 109186491 | ||||||
| chr12:109186636
|
T | G | 1 | a0002c0097t0003g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1980+896T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | chr12 | 109186636 | ||||||
| chr12:109186675
|
G | A | 3 | a0001c0023t0001g0122a0001c0023t0004g0121a0002c0097t0003g0124 | 3 | HG00735.hp2 HG01258.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1980+935G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | chr12 | 109186675 | ||||||
| chr12:109186813
|
C | T | 1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1980+1073C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | chr12 | 109186813 | ||||||
| chr12:109186860
|
C | T | 1 | a0001c0003t0004g0300 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1980+1120C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | chr12 | 109186860 | ||||||
| chr12:109186902
|
C | T | 80 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1981-1097C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | chr12 | 109186902 | ||||||
| chr12:109187196
|
G | A | 4 | a0001c0010t0001g0188a0001c0010t0009g0186a0026c0066t0015g0115others(1): Show | 4 | HG01081.hp1 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-803G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | chr12 | 109187196 | ||||||
| chr12:109187325
|
G | A | 2 | a0001c0064t0009g0184a0007c0037t0004g0073 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1981-674G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | chr12 | 109187325 | ||||||
| chr12:109187431
|
T | TTTTA | 23 | a0001c0002t0001g0085a0001c0003t0002g0099a0001c0022t0004g0005others(20): Show | 23 | HG00099.hp2 HG01884.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.1981-524_1981-521d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | INFO_REALIGN_3_PRIME | chr12 | 109187431 | |||||
| chr12:109187431
|
T | TTTTATTT others(1): Show |
10 | a0001c0004t0007g0001a0001c0004t0007g0011a0001c0004t0007g0019others(7): Show | 11 | HG02083.hp1 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1981-528_1981-521d others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | INFO_REALIGN_3_PRIME | chr12 | 109187431 | |||||
| chr12:109187431
|
TTTTA | T | 26 | a0001c0050t0001g0277a0001c0054t0001g0203a0001c0095t0001g0133others(23): Show | 26 | HG00323.hp1 HG01074.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1981-524_1981-521d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | INFO_REALIGN_3_PRIME | chr12 | 109187431 | |||||
| chr12:109187431
|
TTTTATTT others(5): Show |
T | 2 | a0001c0069t0002g0204a0007c0104t0004g0183 | 2 | HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1981-532_1981-521d others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | INFO_REALIGN_3_PRIME | chr12 | 109187431 | |||||
| chr12:109187803
|
G | A | 1 | a0002c0092t0010g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1981-196G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 12/52 | chr12 | 109187803 | ||||||
| chr12:109188171
|
C | CTCCT | 26 | a0001c0004t0002g0054a0001c0004t0007g0011a0001c0011t0001g0013others(23): Show | 26 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.2144+69_2144+72dup others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109188171 | |||||
| chr12:109188171
|
C | CTCCTTCC others(1): Show |
11 | a0001c0010t0001g0188a0001c0012t0002g0045a0001c0012t0002g0250others(8): Show | 11 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.2144+65_2144+72dup others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109188171 | |||||
| chr12:109188171
|
C | CTCCTTCC others(5): Show |
2 | a0001c0012t0002g0259a0002c0021t0003g0253 | 2 | NA18988.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2144+61_2144+72dup others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109188171 | |||||
| chr12:109188171
|
C | CTCCTTCC others(9): Show |
1 | a0001c0010t0009g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2144+57_2144+72dup others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109188171 | |||||
| chr12:109188171
|
CTCCT | C | 72 | a0001c0002t0001g0098a0001c0003t0002g0094a0001c0003t0002g0101others(69): Show | 72 | HG00323.hp2 HG00408.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.2144+69_2144+72del others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109188171 | |||||
| chr12:109188171
|
CTCCTTCC others(1): Show |
C | 74 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(71): Show | 74 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.2144+65_2144+72del others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109188171 | |||||
| chr12:109188171
|
CTCCTTCC others(5): Show |
C | 30 | a0001c0002t0001g0085a0001c0003t0002g0077a0001c0003t0002g0099others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.2144+61_2144+72del others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109188171 | |||||
| chr12:109188171
|
CTCCTTCC others(9): Show |
C | 26 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0029t0002g0108others(23): Show | 26 | HG01109.hp2 HG01167.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2144+57_2144+72del others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109188171 | |||||
| chr12:109188171
|
CTCCTTCC others(13): Show |
C | 1 | a0002c0006t0005g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2144+53_2144+72del others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109188171 | |||||
| chr12:109188171
|
CTCCTTCC others(17): Show |
C | 1 | a0001c0004t0002g0052 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2144+49_2144+72del others(24): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109188171 | |||||
| chr12:109188218
|
C | T | 2 | a0001c0002t0021g0243a0023c0099t0001g0084 | 2 | NA18950.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2144+56C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109188218 | ||||||
| chr12:109188219
|
TTCCTTCC others(8): Show |
T | 2 | a0001c0002t0021g0243a0023c0099t0001g0084 | 2 | NA18950.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2144+58_2144+72del others(15): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109188219 | ||||||
| chr12:109188222
|
CTTCCTTC others(7): Show |
C | 1 | a0002c0006t0003g0194 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2144+61_2144+74del others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109188222 | ||||||
| chr12:109188230
|
C | T | 1 | a0001c0003t0002g0112 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2144+68C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109188230 | ||||||
| chr12:109188240
|
TC | T | 5 | a0001c0002t0021g0243a0001c0003t0002g0112a0003c0001t0001g0145others(2): Show | 5 | HG03490.hp2 NA18950.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.2144+81delC | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109188240 | |||||
| chr12:109188411
|
TTCCTTCC others(5): Show |
T | 2 | a0004c0008t0001g0227a0009c0096t0009g0295 | 2 | HG02071.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2144+260_2144+271d others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109188411 | |||||
| chr12:109188422
|
C | T | 2 | a0006c0026t0002g0155a0006c0026t0002g0156 | 2 | HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2144+260C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109188422 | ||||||
| chr12:109188423
|
G | T | 140 | a0001c0004t0017g0003a0001c0012t0002g0045a0001c0012t0002g0250others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2144+261G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109188423 | ||||||
| chr12:109188429
|
C | T | 105 | a0001c0004t0017g0003a0001c0012t0002g0045a0001c0012t0002g0250others(102): Show | 105 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.2144+267C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109188429 | ||||||
| chr12:109188666
|
A | T | 306 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.2144+504A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109188666 | ||||||
| chr12:109188847
|
T | C | 4 | a0006c0113t0004g0031a0014c0077t0004g0118a0014c0079t0004g0180others(1): Show | 4 | HG01433.hp1 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2144+685T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109188847 | ||||||
| chr12:109188925
|
G | A | 1 | a0001c0016t0009g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2144+763G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109188925 | ||||||
| chr12:109188972
|
T | C | 248 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.2144+810T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109188972 | ||||||
| chr12:109188991
|
G | A | 1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2144+829G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109188991 | ||||||
| chr12:109189171
|
G | A | 1 | a0001c0124t0012g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2144+1009G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109189171 | ||||||
| chr12:109189392
|
G | A | 1 | a0002c0007t0006g0017 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2144+1230G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109189392 | ||||||
| chr12:109189397
|
A | G | 3 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0016t0009g0290 | 3 | HG02109.hp2 HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2144+1235A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109189397 | ||||||
| chr12:109189435
|
C | T | 5 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(2): Show | 5 | HG03139.hp1 HG03471.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2144+1273C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109189435 | ||||||
| chr12:109189481
|
G | A | 1 | a0001c0054t0001g0203 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2144+1319G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109189481 | ||||||
| chr12:109189594
|
G | C | 1 | a0003c0005t0002g0264 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2144+1432G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109189594 | ||||||
| chr12:109189599
|
A | G | 2 | a0001c0069t0002g0204a0017c0123t0015g0058 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2144+1437A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109189599 | ||||||
| chr12:109189611
|
A | G | 239 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2144+1449A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109189611 | ||||||
| chr12:109189653
|
C | T | 1 | a0002c0043t0003g0012 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2144+1491C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109189653 | ||||||
| chr12:109189654
|
G | A | 8 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(5): Show | 8 | HG01433.hp1 HG03139.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2144+1492G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109189654 | ||||||
| chr12:109189780
|
G | A | 9 | a0001c0105t0004g0296a0001c0106t0001g0293a0002c0006t0005g0294others(6): Show | 9 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.2144+1618G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109189780 | ||||||
| chr12:109189870
|
G | A | 9 | a0001c0023t0001g0122a0001c0023t0004g0121a0001c0050t0001g0277others(6): Show | 9 | HG00735.hp2 HG01074.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.2144+1708G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109189870 | ||||||
| chr12:109189931
|
C | T | 5 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(2): Show | 5 | HG03139.hp1 HG03471.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2145-1682C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109189931 | ||||||
| chr12:109190107
|
G | T | 40 | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0009g0186others(37): Show | 40 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.2145-1506G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109190107 | ||||||
| chr12:109190233
|
C | A | 2 | a0026c0066t0015g0115a0027c0065t0005g0225 | 2 | HG01081.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2145-1380C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109190233 | ||||||
| chr12:109190300
|
C | G | 9 | a0001c0023t0001g0122a0001c0023t0004g0121a0001c0050t0001g0277others(6): Show | 9 | HG00735.hp2 HG01074.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.2145-1313C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109190300 | ||||||
| chr12:109190368
|
G | A | 2 | a0001c0013t0001g0163a0011c0027t0004g0249 | 2 | HG00544.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2145-1245G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109190368 | ||||||
| chr12:109190397
|
G | A | 2 | a0001c0034t0001g0211a0001c0034t0001g0212 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.2145-1216G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109190397 | ||||||
| chr12:109190478
|
C | T | 1 | a0001c0124t0012g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2145-1135C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109190478 | ||||||
| chr12:109190595
|
A | G | 26 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(23): Show | 26 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.2145-1018A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109190595 | ||||||
| chr12:109190626
|
G | GT | 237 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.2145-978dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109190626 | |||||
| chr12:109190626
|
GTT | G | 8 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(5): Show | 8 | HG01433.hp1 HG03139.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2145-979_2145-978d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109190626 | |||||
| chr12:109190654
|
G | A | 27 | a0001c0004t0017g0003a0001c0038t0001g0201a0002c0070t0005g0199others(24): Show | 27 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.2145-959G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109190654 | ||||||
| chr12:109190924
|
C | T | 3 | a0001c0016t0011g0274a0007c0057t0004g0207a0009c0096t0009g0295 | 3 | HG02965.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2145-689C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109190924 | ||||||
| chr12:109190965
|
A | G | 1 | a0002c0088t0006g0247 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2145-648A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109190965 | ||||||
| chr12:109190989
|
G | A | 55 | a0001c0011t0001g0013a0001c0013t0001g0163a0001c0023t0001g0089others(52): Show | 55 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.2145-624G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109190989 | ||||||
| chr12:109191165
|
C | T | 89 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.2145-448C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109191165 | ||||||
| chr12:109191212
|
C | CCTGTGCT others(1): Show |
8 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(5): Show | 8 | HG01433.hp1 HG03139.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2145-401_2145-400i others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109191212 | ||||||
| chr12:109191215
|
C | CT | 87 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.2145-383dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109191215 | |||||
| chr12:109191215
|
CT | C | 41 | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0009g0186others(38): Show | 41 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.2145-383delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109191215 | |||||
| chr12:109191216
|
T | TTTTC | 8 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(5): Show | 8 | HG01433.hp1 HG03139.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2145-394_2145-393i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | 109191216 | |||||
| chr12:109191236
|
C | T | 8 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(5): Show | 8 | HG01433.hp1 HG03139.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2145-377C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | chr12 | 109191236 | ||||||
| chr12:109192190
|
C | T | 88 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2399+240C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109192190 | ||||||
| chr12:109192271
|
G | A | 17 | a0005c0056t0003g0053a0006c0026t0002g0155a0006c0026t0002g0156others(14): Show | 17 | HG00323.hp1 HG01081.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2399+321G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109192271 | ||||||
| chr12:109192336
|
T | A | 4 | a0001c0054t0001g0203a0001c0055t0001g0226a0002c0053t0005g0033others(1): Show | 4 | HG01943.hp2 HG02922.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2399+386T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109192336 | ||||||
| chr12:109192483
|
C | T | 1 | a0007c0057t0004g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2399+533C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109192483 | ||||||
| chr12:109192654
|
A | T | 1 | a0001c0039t0004g0116 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2399+704A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109192654 | ||||||
| chr12:109192671
|
A | G | 3 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0016t0009g0290 | 3 | HG02109.hp2 HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2399+721A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109192671 | ||||||
| chr12:109192746
|
G | T | 41 | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0009g0186others(38): Show | 41 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.2399+796G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109192746 | ||||||
| chr12:109192874
|
C | G | 22 | a0001c0016t0009g0287a0001c0016t0009g0305a0001c0032t0004g0291others(19): Show | 22 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.2400-774C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109192874 | ||||||
| chr12:109192877
|
G | A | 4 | a0001c0054t0001g0203a0001c0055t0001g0226a0002c0053t0005g0033others(1): Show | 4 | HG01943.hp2 HG02922.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-771G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109192877 | ||||||
| chr12:109192910
|
C | A | 1 | a0003c0005t0002g0264 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2400-738C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109192910 | ||||||
| chr12:109192982
|
T | G | 6 | a0001c0016t0009g0287a0001c0016t0009g0305a0001c0032t0004g0291others(3): Show | 6 | HG01081.hp1 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2400-666T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109192982 | ||||||
| chr12:109193016
|
T | C | 81 | a0001c0011t0001g0013a0001c0012t0002g0045a0001c0012t0002g0250others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2400-632T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109193016 | ||||||
| chr12:109193196
|
T | A | 1 | a0002c0092t0010g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2400-452T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109193196 | ||||||
| chr12:109193217
|
CT | C | 281 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0081others(278): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.2400-413delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | INFO_REALIGN_3_PRIME | chr12 | 109193217 | |||||
| chr12:109193217
|
CTTTTTTT others(3): Show |
C | 8 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(5): Show | 8 | HG01433.hp1 HG03139.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2400-422_2400-413d others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | INFO_REALIGN_3_PRIME | chr12 | 109193217 | |||||
| chr12:109193303
|
C | T | 1 | a0001c0011t0001g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2400-345C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109193303 | ||||||
| chr12:109193480
|
G | A | 21 | a0001c0016t0009g0287a0001c0016t0009g0305a0001c0032t0004g0291others(18): Show | 21 | HG00323.hp1 HG01081.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.2400-168G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | chr12 | 109193480 | ||||||
| chr12:109193742
|
G | A | 2 | a0001c0069t0002g0204a0017c0123t0015g0058 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2481+13G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109193742 | ||||||
| chr12:109193746
|
C | T | 1 | a0006c0026t0016g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2481+17C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109193746 | ||||||
| chr12:109193882
|
C | T | 1 | a0002c0036t0006g0223 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2481+153C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109193882 | ||||||
| chr12:109193968
|
C | T | 2 | a0008c0015t0005g0171a0008c0015t0005g0172 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2481+239C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109193968 | ||||||
| chr12:109194009
|
T | G | 220 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2481+280T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194009 | ||||||
| chr12:109194016
|
G | T | 90 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2481+287G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194016 | ||||||
| chr12:109194054
|
G | C | 3 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0016t0009g0290 | 3 | HG02109.hp2 HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2481+325G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194054 | ||||||
| chr12:109194100
|
A | C | 80 | a0001c0011t0001g0013a0001c0012t0002g0045a0001c0012t0002g0250others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2481+371A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194100 | ||||||
| chr12:109194183
|
T | TTTG | 12 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0002g0103others(9): Show | 12 | HG02109.hp1 HG02486.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.2481+456_2481+457i others(5): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194183 | |||||
| chr12:109194186
|
T | G | 139 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.2481+457T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194186 | ||||||
| chr12:109194189
|
T | G | 251 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.2481+460T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194189 | ||||||
| chr12:109194192
|
G | T | 2 | a0001c0029t0002g0108a0002c0007t0022g0032 | 2 | HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2481+463G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194192 | ||||||
| chr12:109194210
|
T | G | 91 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2481+481T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194210 | ||||||
| chr12:109194280
|
C | G | 2 | a0001c0069t0002g0204a0017c0123t0015g0058 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2481+551C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194280 | ||||||
| chr12:109194475
|
G | T | 91 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2481+746G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194475 | ||||||
| chr12:109194475
|
GCATGAGC others(101): Show |
G | 4 | a0001c0016t0009g0287a0001c0032t0004g0291a0001c0032t0004g0292others(1): Show | 4 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2481+761_2481+868d others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194475 | |||||
| chr12:109194490
|
C | T | 17 | a0001c0016t0009g0305a0005c0056t0003g0053a0006c0026t0002g0155others(14): Show | 17 | HG00323.hp1 HG01081.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2481+761C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194490 | ||||||
| chr12:109194491
|
A | G | 116 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2481+762A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194491 | ||||||
| chr12:109194492
|
A | G | 116 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2481+763A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194492 | ||||||
| chr12:109194504
|
GTGTGTGC others(99): Show |
G | 5 | a0001c0105t0004g0296a0001c0106t0001g0293a0002c0006t0005g0294others(2): Show | 5 | HG02809.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2481+782_2481+887d others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194504 | |||||
| chr12:109194506
|
GTGTGCAT others(97): Show |
G | 20 | a0001c0003t0002g0102a0001c0003t0004g0074a0001c0016t0009g0305others(17): Show | 20 | HG01168.hp1 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.2481+782_2481+885d others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194506 | |||||
| chr12:109194508
|
GTGCA | G | 5 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(2): Show | 5 | HG03139.hp1 HG03471.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2481+782_2481+785d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194508 | |||||
| chr12:109194508
|
GTGCATGT others(95): Show |
G | 14 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0300others(11): Show | 14 | HG00323.hp1 HG01081.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2481+782_2481+883d others(2): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194508 | |||||
| chr12:109194510
|
GCA | G | 13 | a0001c0002t0001g0109a0001c0002t0001g0241a0001c0002t0001g0242others(10): Show | 13 | HG01069.hp1 HG01192.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.2481+782_2481+783d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194510 | ||||||
| chr12:109194510
|
GCATGTGT others(91): Show |
G | 16 | a0001c0002t0001g0035a0001c0003t0002g0077a0001c0003t0002g0101others(13): Show | 16 | HG00558.hp1 HG00639.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.2481+782_2481+879d others(100): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194510 | ||||||
| chr12:109194510
|
GCATGTGT others(93): Show |
G | 40 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0081others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.2481+782_2481+881d others(102): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194510 | ||||||
| chr12:109194511
|
C | CGT | 3 | a0003c0001t0001g0137a0019c0093t0001g0159a0022c0084t0004g0254 | 3 | HG00609.hp2 HG02080.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.2481+782_2481+783i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194511 | ||||||
| chr12:109194511
|
C | CGTGT | 12 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0013t0001g0153others(9): Show | 12 | HG00673.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.2481+782_2481+783i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194511 | ||||||
| chr12:109194511
|
C | CGTGTGT | 45 | a0001c0011t0001g0013a0001c0012t0002g0251a0001c0012t0002g0259others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2481+782_2481+783i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194511 | ||||||
| chr12:109194511
|
C | CGTGTGTG others(1): Show |
19 | a0001c0013t0001g0163a0001c0013t0001g0248a0001c0013t0001g0256others(16): Show | 19 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.2481+782_2481+783i others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194511 | ||||||
| chr12:109194511
|
CAT | C | 3 | a0006c0113t0004g0031a0014c0079t0004g0180a0015c0114t0004g0009 | 3 | HG01433.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2481+783_2481+784d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194511 | ||||||
| chr12:109194512
|
A | ATG | 6 | a0001c0069t0002g0204a0002c0007t0003g0014a0002c0017t0024g0044others(3): Show | 6 | HG01943.hp1 HG02896.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2481+819_2481+820d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194512 | |||||
| chr12:109194512
|
A | ATGTG | 11 | a0001c0023t0001g0122a0001c0023t0004g0121a0001c0050t0001g0277others(8): Show | 11 | HG00735.hp2 HG01074.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.2481+817_2481+820d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194512 | |||||
| chr12:109194512
|
A | ATGTGTG | 3 | a0004c0008t0008g0216a0004c0041t0002g0222a0010c0042t0003g0220 | 3 | HG01167.hp1 HG01169.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.2481+815_2481+820d others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194512 | |||||
| chr12:109194512
|
A | ATGTGTGT others(1): Show |
3 | a0001c0064t0009g0184a0001c0124t0012g0197a0007c0037t0004g0073 | 3 | HG02280.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2481+813_2481+820d others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194512 | |||||
| chr12:109194512
|
A | ATGTGTGT others(3): Show |
14 | a0001c0038t0001g0201a0004c0008t0001g0198a0004c0008t0001g0218others(11): Show | 14 | HG00642.hp2 HG02071.hp1 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.2481+811_2481+820d others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194512 | |||||
| chr12:109194512
|
A | ATGTGTGT others(5): Show |
6 | a0004c0008t0008g0263a0006c0031t0004g0002a0006c0031t0004g0206others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2481+809_2481+820d others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194512 | |||||
| chr12:109194512
|
A | ATGTGTGT others(7): Show |
4 | a0001c0004t0017g0003a0001c0016t0011g0274a0002c0070t0005g0199others(1): Show | 4 | HG02965.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2481+807_2481+820d others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194512 | |||||
| chr12:109194512
|
A | ATGTGTGT others(11): Show |
1 | a0004c0040t0002g0215 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2481+803_2481+820d others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194512 | |||||
| chr12:109194512
|
A | G | 81 | a0001c0011t0001g0013a0001c0012t0002g0045a0001c0012t0002g0250others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2481+783A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194512 | ||||||
| chr12:109194512
|
ATGTGTGT others(3): Show |
A | 1 | a0017c0123t0015g0058 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2481+811_2481+820d others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194512 | |||||
| chr12:109194516
|
GTGTGTGT others(87): Show |
G | 7 | a0001c0002t0001g0109a0001c0002t0001g0242a0001c0048t0002g0281others(4): Show | 7 | HG01192.hp1 HG03490.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.2481+821_2481+914d others(96): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194516 | |||||
| chr12:109194517
|
T | C | 5 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(2): Show | 5 | HG03139.hp1 HG03471.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2481+788T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194517 | ||||||
| chr12:109194518
|
GTGTGTGT others(85): Show |
G | 4 | a0001c0002t0001g0241a0001c0002t0008g0306a0001c0023t0001g0100others(1): Show | 4 | HG01069.hp1 HG01515.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.2481+821_2481+912d others(94): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194518 | |||||
| chr12:109194520
|
GTGTGTGT others(83): Show |
G | 1 | a0002c0006t0003g0194 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2481+821_2481+910d others(92): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194520 | |||||
| chr12:109194522
|
GTGTGTGT others(81): Show |
G | 1 | a0001c0049t0004g0088 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2481+821_2481+908d others(90): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194522 | |||||
| chr12:109194610
|
C | CTG | 20 | a0001c0011t0001g0056a0001c0016t0009g0287a0001c0022t0004g0004others(17): Show | 20 | HG00609.hp1 HG00735.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.2481+919_2481+920d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194610 | |||||
| chr12:109194610
|
C | CTGTGTGT others(3): Show |
1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2481+911_2481+920d others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194610 | |||||
| chr12:109194610
|
C | G | 16 | a0001c0002t0001g0035a0001c0003t0002g0077a0001c0003t0002g0101others(13): Show | 16 | HG00558.hp1 HG00639.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.2481+881C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194610 | ||||||
| chr12:109194610
|
CTG | C | 13 | a0001c0004t0002g0050a0001c0012t0002g0045a0001c0012t0002g0250others(10): Show | 13 | HG00673.hp1 HG01884.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.2481+919_2481+920d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194610 | |||||
| chr12:109194610
|
CTGTG | C | 29 | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0009g0186others(26): Show | 29 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.2481+917_2481+920d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194610 | |||||
| chr12:109194610
|
CTGTGTG | C | 26 | a0001c0064t0009g0184a0001c0095t0001g0133a0001c0098t0001g0286others(23): Show | 26 | HG00642.hp2 HG01109.hp2 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.2481+915_2481+920d others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194610 | |||||
| chr12:109194610
|
CTGTGTGT others(1): Show |
C | 54 | a0001c0011t0001g0013a0001c0013t0001g0163a0001c0029t0011g0090others(51): Show | 54 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.2481+913_2481+920d others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109194610 | |||||
| chr12:109194715
|
T | C | 11 | a0001c0016t0011g0274a0001c0022t0004g0004a0001c0022t0004g0005others(8): Show | 11 | HG01433.hp1 HG02965.hp1 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.2481+986T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194715 | ||||||
| chr12:109194787
|
A | C | 3 | a0001c0016t0011g0274a0007c0057t0004g0207a0009c0096t0009g0295 | 3 | HG02965.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2481+1058A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194787 | ||||||
| chr12:109194809
|
C | T | 1 | a0006c0113t0004g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2481+1080C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194809 | ||||||
| chr12:109194841
|
A | G | 26 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(23): Show | 26 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.2481+1112A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194841 | ||||||
| chr12:109194884
|
C | T | 1 | a0037c0072t0001g0217 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2481+1155C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194884 | ||||||
| chr12:109194947
|
A | T | 125 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2481+1218A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194947 | ||||||
| chr12:109194953
|
A | G | 125 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2481+1224A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194953 | ||||||
| chr12:109194993
|
C | T | 1 | a0004c0008t0008g0216 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2481+1264C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109194993 | ||||||
| chr12:109195152
|
G | T | 1 | a0001c0039t0004g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2481+1423G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109195152 | ||||||
| chr12:109195262
|
G | C | 1 | a0002c0092t0010g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2481+1533G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109195262 | ||||||
| chr12:109195474
|
C | T | 1 | a0002c0007t0003g0026 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2482-1534C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109195474 | ||||||
| chr12:109195511
|
T | C | 146 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2482-1497T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109195511 | ||||||
| chr12:109195680
|
C | T | 1 | a0027c0065t0005g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2482-1328C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109195680 | ||||||
| chr12:109195726
|
G | GT | 38 | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0009g0186others(35): Show | 38 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.2482-1272dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | 109195726 | |||||
| chr12:109195908
|
G | A | 243 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.2482-1100G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109195908 | ||||||
| chr12:109195987
|
T | C | 91 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2482-1021T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109195987 | ||||||
| chr12:109196034
|
A | G | 8 | a0001c0105t0004g0296a0001c0106t0001g0293a0002c0006t0005g0294others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.2482-974A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109196034 | ||||||
| chr12:109196128
|
T | C | 146 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2482-880T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109196128 | ||||||
| chr12:109196137
|
G | T | 1 | a0004c0112t0001g0119 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2482-871G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109196137 | ||||||
| chr12:109196350
|
A | G | 272 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2482-658A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109196350 | ||||||
| chr12:109196405
|
G | C | 3 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0016t0009g0290 | 3 | HG02109.hp2 HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2482-603G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109196405 | ||||||
| chr12:109196451
|
C | T | 38 | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0009g0186others(35): Show | 38 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.2482-557C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109196451 | ||||||
| chr12:109196751
|
C | T | 1 | a0006c0078t0001g0181 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2482-257C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109196751 | ||||||
| chr12:109196776
|
C | T | 1 | a0001c0011t0001g0008 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2482-232C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109196776 | ||||||
| chr12:109196916
|
A | G | 1 | a0003c0001t0004g0139 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2482-92A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109196916 | ||||||
| chr12:109196949
|
A | G | 1 | a0002c0007t0003g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2482-59A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | 109196949 | ||||||
| chr12:109197226
|
A | G | 155 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2627+73A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109197226 | ||||||
| chr12:109197249
|
G | A | 17 | a0005c0056t0003g0053a0006c0026t0002g0155a0006c0026t0002g0156others(14): Show | 17 | HG00323.hp1 HG01081.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2627+96G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109197249 | ||||||
| chr12:109197271
|
T | C | 138 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.2627+118T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109197271 | ||||||
| chr12:109197401
|
G | A | 3 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0016t0009g0290 | 3 | HG02109.hp2 HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2627+248G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109197401 | ||||||
| chr12:109197441
|
C | T | 91 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2627+288C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109197441 | ||||||
| chr12:109197472
|
T | C | 243 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.2627+319T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109197472 | ||||||
| chr12:109197493
|
G | A | 1 | a0003c0005t0002g0134 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2627+340G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109197493 | ||||||
| chr12:109197525
|
C | T | 15 | a0005c0056t0003g0053a0006c0026t0002g0155a0006c0026t0002g0156others(12): Show | 15 | HG00323.hp1 HG02280.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.2627+372C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109197525 | ||||||
| chr12:109197837
|
A | T | 1 | a0003c0001t0001g0149 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2627+684A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109197837 | ||||||
| chr12:109197863
|
A | G | 2 | a0026c0066t0015g0115a0027c0065t0005g0225 | 2 | HG01081.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2627+710A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109197863 | ||||||
| chr12:109198044
|
T | C | 138 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.2627+891T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109198044 | ||||||
| chr12:109198354
|
G | T | 3 | a0006c0113t0004g0031a0014c0079t0004g0180a0015c0114t0004g0009 | 3 | HG01433.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2628-1048G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109198354 | ||||||
| chr12:109198565
|
G | A | 2 | a0001c0064t0009g0184a0007c0037t0004g0073 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2628-837G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109198565 | ||||||
| chr12:109198634
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2628-768C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109198634 | ||||||
| chr12:109198711
|
C | A | 4 | a0001c0018t0002g0048a0001c0018t0002g0049a0001c0018t0011g0046others(1): Show | 4 | HG01070.hp2 HG01123.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.2628-691C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109198711 | ||||||
| chr12:109198777
|
C | T | 31 | a0001c0004t0017g0003a0001c0038t0001g0201a0001c0095t0001g0133others(28): Show | 31 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.2628-625C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109198777 | ||||||
| chr12:109198799
|
T | A | 1 | a0002c0014t0003g0106 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2628-603T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109198799 | ||||||
| chr12:109198822
|
C | T | 4 | a0001c0054t0001g0203a0001c0055t0001g0226a0002c0053t0005g0033others(1): Show | 4 | HG01943.hp2 HG02922.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2628-580C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109198822 | ||||||
| chr12:109198864
|
C | G | 154 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.2628-538C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109198864 | ||||||
| chr12:109198963
|
G | A | 1 | a0001c0002t0001g0035 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2628-439G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109198963 | ||||||
| chr12:109198976
|
A | T | 1 | a0002c0092t0010g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2628-426A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109198976 | ||||||
| chr12:109199083
|
G | A | 2 | a0006c0078t0001g0181a0008c0044t0003g0182 | 2 | NA18992.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2628-319G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109199083 | ||||||
| chr12:109199307
|
C | T | 1 | a0030c0071t0002g0040 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2628-95C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109199307 | ||||||
| chr12:109199335
|
C | T | 1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2628-67C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109199335 | ||||||
| chr12:109199383
|
G | C | 154 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.2628-19G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 17/52 | chr12 | 109199383 | ||||||
| chr12:109199557
|
C | T | 1 | a0006c0078t0001g0181 | 1 | NA19060.hp2 | splice_region_variant&intron_variant | LOW | c.2778+5C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109199557 | ||||||
| chr12:109199567
|
G | C | 1 | a0001c0003t0002g0112 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2778+15G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109199567 | ||||||
| chr12:109199744
|
T | C | 9 | a0001c0023t0001g0122a0001c0023t0004g0121a0001c0050t0001g0277others(6): Show | 9 | HG00735.hp2 HG01074.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.2778+192T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109199744 | ||||||
| chr12:109199774
|
G | A | 1 | a0002c0092t0010g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2778+222G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109199774 | ||||||
| chr12:109199836
|
A | G | 1 | a0011c0027t0013g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2778+284A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109199836 | ||||||
| chr12:109199840
|
C | T | 90 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2778+288C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109199840 | ||||||
| chr12:109199905
|
C | T | 1 | a0001c0029t0002g0096 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2778+353C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109199905 | ||||||
| chr12:109200004
|
C | T | 8 | a0001c0105t0004g0296a0001c0106t0001g0293a0002c0006t0005g0294others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.2778+452C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109200004 | ||||||
| chr12:109200010
|
C | T | 1 | a0009c0103t0004g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2778+458C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109200010 | ||||||
| chr12:109200031
|
C | CA | 31 | a0001c0003t0002g0103a0001c0003t0002g0244a0001c0023t0001g0100others(28): Show | 31 | HG00323.hp1 HG00609.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.2778+497dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr12 | 109200031 | |||||
| chr12:109200031
|
CA | C | 10 | a0001c0002t0001g0081a0001c0010t0002g0261a0001c0022t0004g0004others(7): Show | 10 | HG00639.hp2 HG00642.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.2778+497delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr12 | 109200031 | |||||
| chr12:109200066
|
T | A | 1 | a0004c0008t0001g0198 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2778+514T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109200066 | ||||||
| chr12:109200196
|
T | C | 1 | a0001c0038t0001g0029 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2778+644T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109200196 | ||||||
| chr12:109200462
|
G | T | 1 | a0014c0079t0004g0180 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2778+910G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109200462 | ||||||
| chr12:109200720
|
A | G | 2 | a0011c0027t0004g0150a0011c0027t0013g0065 | 2 | HG01168.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.2779-847A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109200720 | ||||||
| chr12:109200790
|
A | G | 1 | a0002c0020t0003g0273 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2779-777A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109200790 | ||||||
| chr12:109200952
|
T | TG | 5 | a0003c0001t0001g0145a0003c0001t0001g0154a0003c0001t0001g0297others(2): Show | 5 | HG00621.hp2 NA18946.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.2779-613dupG | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr12 | 109200952 | |||||
| chr12:109200955
|
T | G | 254 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.2779-612T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109200955 | ||||||
| chr12:109201065
|
G | A | 5 | a0001c0016t0011g0274a0001c0069t0002g0204a0007c0057t0004g0207others(2): Show | 5 | HG01884.hp1 HG02965.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2779-502G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109201065 | ||||||
| chr12:109201171
|
C | G | 8 | a0001c0105t0004g0296a0001c0106t0001g0293a0002c0006t0005g0294others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.2779-396C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109201171 | ||||||
| chr12:109201452
|
T | C | 1 | a0039c0080t0010g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2779-115T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109201452 | ||||||
| chr12:109201525
|
A | G | 1 | a0001c0023t0004g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2779-42A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | chr12 | 109201525 | ||||||
| chr12:109201716
|
G | A | 48 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0016t0009g0290others(45): Show | 48 | HG00323.hp1 HG00642.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.2913+15G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109201716 | ||||||
| chr12:109201795
|
C | T | 1 | a0001c0003t0002g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2913+94C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109201795 | ||||||
| chr12:109201804
|
T | C | 109 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.2913+103T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109201804 | ||||||
| chr12:109201950
|
A | G | 1 | a0029c0085t0003g0238 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2913+249A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109201950 | ||||||
| chr12:109201987
|
C | T | 19 | a0004c0008t0001g0198a0004c0008t0001g0218a0004c0008t0001g0221others(16): Show | 19 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913+286C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109201987 | ||||||
| chr12:109202226
|
TG | T | 94 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.2913+526delG | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109202226 | ||||||
| chr12:109202409
|
G | T | 1 | a0001c0055t0001g0226 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2913+708G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109202409 | ||||||
| chr12:109202502
|
A | T | 1 | a0005c0019t0006g0076 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2913+801A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109202502 | ||||||
| chr12:109202708
|
G | A | 4 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(1): Show | 4 | HG03139.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913+1007G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109202708 | ||||||
| chr12:109202945
|
G | A | 163 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.2913+1244G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109202945 | ||||||
| chr12:109203150
|
C | T | 2 | a0001c0095t0001g0133a0001c0098t0001g0286 | 2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2913+1449C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109203150 | ||||||
| chr12:109203330
|
G | C | 1 | a0001c0060t0002g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2913+1629G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109203330 | ||||||
| chr12:109203356
|
C | T | 1 | a0001c0003t0002g0068 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2913+1655C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109203356 | ||||||
| chr12:109203357
|
A | G | 159 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.2913+1656A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109203357 | ||||||
| chr12:109203458
|
G | A | 131 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.2913+1757G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109203458 | ||||||
| chr12:109203538
|
A | G | 1 | a0015c0114t0004g0009 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2913+1837A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109203538 | ||||||
| chr12:109203556
|
TGCTC | T | 5 | a0001c0016t0011g0274a0001c0069t0002g0204a0007c0057t0004g0207others(2): Show | 5 | HG01884.hp1 HG02965.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2913+1859_2913+186 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109203556 | |||||
| chr12:109203600
|
T | C | 1 | a0018c0051t0023g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2913+1899T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109203600 | ||||||
| chr12:109203773
|
G | C | 90 | a0001c0011t0001g0013a0001c0012t0002g0045a0001c0012t0002g0250others(87): Show | 90 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.2913+2072G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109203773 | ||||||
| chr12:109203783
|
C | T | 3 | a0006c0113t0004g0031a0014c0079t0004g0180a0015c0114t0004g0009 | 3 | HG01433.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2913+2082C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109203783 | ||||||
| chr12:109203814
|
G | A | 3 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0016t0009g0290 | 3 | HG02109.hp2 HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2913+2113G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109203814 | ||||||
| chr12:109204028
|
T | A | 91 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2913+2327T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204028 | ||||||
| chr12:109204050
|
G | C | 1 | a0002c0021t0006g0255 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2913+2349G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204050 | ||||||
| chr12:109204160
|
T | A | 80 | a0001c0011t0001g0013a0001c0012t0002g0045a0001c0012t0002g0250others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2913+2459T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204160 | ||||||
| chr12:109204173
|
G | A | 80 | a0001c0011t0001g0013a0001c0012t0002g0045a0001c0012t0002g0250others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2913+2472G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204173 | ||||||
| chr12:109204218
|
C | T | 1 | a0002c0061t0003g0062 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2914-2492C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204218 | ||||||
| chr12:109204222
|
C | T | 24 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0016t0009g0287others(21): Show | 24 | HG00323.hp1 HG01081.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.2914-2488C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204222 | ||||||
| chr12:109204271
|
C | CT | 85 | a0001c0011t0001g0008a0001c0011t0001g0013a0001c0012t0002g0045others(82): Show | 85 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.2914-2419dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109204271 | |||||
| chr12:109204271
|
CT | C | 139 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.2914-2419delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109204271 | |||||
| chr12:109204271
|
CTT | C | 6 | a0001c0016t0011g0274a0001c0018t0002g0048a0001c0062t0019g0288others(3): Show | 6 | HG01070.hp2 HG01168.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2914-2420_2914-241 others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109204271 | |||||
| chr12:109204305
|
G | A | 2 | a0001c0010t0001g0188a0001c0010t0009g0186 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2914-2405G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204305 | ||||||
| chr12:109204335
|
C | T | 2 | a0001c0069t0002g0204a0017c0123t0015g0058 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2914-2375C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204335 | ||||||
| chr12:109204457
|
T | C | 30 | a0001c0004t0017g0003a0001c0095t0001g0133a0001c0098t0001g0286others(27): Show | 30 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.2914-2253T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204457 | ||||||
| chr12:109204512
|
T | A | 92 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.2914-2198T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204512 | ||||||
| chr12:109204539
|
T | C | 1 | a0002c0092t0010g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2914-2171T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204539 | ||||||
| chr12:109204551
|
A | G | 2 | a0001c0095t0001g0133a0001c0098t0001g0286 | 2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2914-2159A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204551 | ||||||
| chr12:109204571
|
A | G | 1 | a0003c0005t0002g0264 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2914-2139A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204571 | ||||||
| chr12:109204576
|
C | T | 1 | a0007c0030t0004g0285 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2914-2134C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204576 | ||||||
| chr12:109204610
|
T | C | 1 | a0002c0006t0005g0123 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2914-2100T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204610 | ||||||
| chr12:109204768
|
C | T | 19 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0016t0009g0290others(16): Show | 19 | HG00323.hp1 HG02109.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.2914-1942C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204768 | ||||||
| chr12:109204897
|
T | A | 1 | a0001c0046t0002g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2914-1813T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204897 | ||||||
| chr12:109204995
|
A | G | 2 | a0001c0064t0009g0184a0007c0037t0004g0073 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2914-1715A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109204995 | ||||||
| chr12:109205010
|
T | C | 1 | a0002c0007t0003g0041 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2914-1700T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109205010 | ||||||
| chr12:109205097
|
G | A | 1 | a0001c0002t0001g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2914-1613G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109205097 | ||||||
| chr12:109205287
|
T | C | 1 | a0001c0003t0004g0074 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2914-1423T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109205287 | ||||||
| chr12:109205333
|
C | T | 1 | a0003c0001t0004g0266 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2914-1377C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109205333 | ||||||
| chr12:109205342
|
C | T | 1 | a0040c0115t0001g0258 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2914-1368C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109205342 | ||||||
| chr12:109205347
|
A | G | 64 | a0001c0002t0001g0079a0001c0002t0001g0081a0001c0003t0002g0244others(61): Show | 64 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2914-1363A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109205347 | ||||||
| chr12:109205454
|
C | CT | 10 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0300others(7): Show | 10 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2914-1243dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109205454 | |||||
| chr12:109205559
|
C | T | 1 | a0001c0029t0011g0090 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2914-1151C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109205559 | ||||||
| chr12:109205719
|
G | A | 1 | a0002c0006t0003g0111 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2914-991G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109205719 | ||||||
| chr12:109205840
|
G | A | 55 | a0001c0002t0001g0079a0001c0002t0001g0191a0001c0002t0001g0235others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2914-870G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109205840 | ||||||
| chr12:109205890
|
A | G | 63 | a0001c0002t0001g0035a0001c0002t0001g0081a0001c0002t0001g0098others(60): Show | 63 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.2914-820A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109205890 | ||||||
| chr12:109205973
|
G | A | 25 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0064t0009g0184others(22): Show | 25 | HG00323.hp1 HG02145.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.2914-737G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109205973 | ||||||
| chr12:109206105
|
A | G | 2 | a0007c0104t0004g0183a0015c0114t0004g0009 | 2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2914-605A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109206105 | ||||||
| chr12:109206109
|
G | C | 1 | a0002c0014t0003g0106 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2914-601G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109206109 | ||||||
| chr12:109206111
|
T | C | 2 | a0002c0007t0003g0037a0002c0007t0003g0041 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2914-599T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109206111 | ||||||
| chr12:109206223
|
C | T | 16 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(13): Show | 16 | HG02257.hp1 HG02523.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2914-487C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109206223 | ||||||
| chr12:109206259
|
A | C | 33 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(30): Show | 33 | HG00323.hp1 HG01081.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.2914-451A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109206259 | ||||||
| chr12:109206428
|
C | CA | 14 | a0001c0002t0001g0081a0001c0012t0002g0262a0001c0046t0002g0067others(11): Show | 14 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.2914-266dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109206428 | |||||
| chr12:109206428
|
C | CAAA | 55 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0091others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.2914-268_2914-266d others(5): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109206428 | |||||
| chr12:109206428
|
C | CAAAA | 6 | a0001c0002t0001g0235a0003c0001t0001g0087a0003c0001t0001g0138others(3): Show | 6 | HG00741.hp2 HG01106.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.2914-269_2914-266d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109206428 | |||||
| chr12:109206428
|
C | CAAAAAAA others(3): Show |
2 | a0001c0064t0009g0184a0007c0037t0004g0073 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2914-275_2914-266d others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109206428 | |||||
| chr12:109206428
|
C | CAAAAAAA others(4): Show |
5 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(2): Show | 5 | HG02559.hp1 HG03139.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.2914-276_2914-266d others(13): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109206428 | |||||
| chr12:109206428
|
C | CAAAAAAA others(5): Show |
25 | a0001c0022t0004g0007a0001c0039t0004g0039a0001c0039t0004g0116others(22): Show | 25 | HG00323.hp1 HG01433.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.2914-277_2914-266d others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109206428 | |||||
| chr12:109206428
|
C | CAAAAAAA others(6): Show |
5 | a0001c0016t0009g0290a0002c0092t0010g0192a0006c0026t0002g0156others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.2914-278_2914-266d others(15): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109206428 | |||||
| chr12:109206428
|
C | CAAAAAAA others(7): Show |
3 | a0001c0016t0009g0287a0001c0032t0004g0291a0001c0032t0004g0292 | 3 | HG02896.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2914-279_2914-266d others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109206428 | |||||
| chr12:109206428
|
C | CAAAAAAA others(8): Show |
3 | a0001c0010t0009g0186a0001c0016t0009g0305a0002c0118t0005g0231 | 3 | HG02258.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2914-280_2914-266d others(17): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109206428 | |||||
| chr12:109206428
|
C | CAAAAAAA others(9): Show |
2 | a0009c0025t0001g0105a0009c0025t0001g0270 | 2 | HG01069.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2914-281_2914-266d others(18): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109206428 | |||||
| chr12:109206428
|
C | CAAAAAAA others(10): Show |
4 | a0009c0025t0001g0269a0009c0025t0001g0301a0017c0123t0015g0058others(1): Show | 4 | HG01106.hp2 HG01258.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.2914-266_2914-265i others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109206428 | |||||
| chr12:109206428
|
C | CAAAAAAA others(11): Show |
2 | a0001c0003t0004g0074a0027c0065t0005g0225 | 2 | HG01081.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2914-266_2914-265i others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109206428 | |||||
| chr12:109206428
|
C | CAAAAAAA others(12): Show |
1 | a0006c0113t0004g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2914-266_2914-265i others(21): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | 109206428 | |||||
| chr12:109206552
|
G | A | 119 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0091others(116): Show | 119 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.2914-158G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109206552 | ||||||
| chr12:109206598
|
A | AG | 11 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(8): Show | 11 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.2914-112_2914-111i others(3): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109206598 | ||||||
| chr12:109206599
|
T | A | 11 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(8): Show | 11 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.2914-111T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109206599 | ||||||
| chr12:109206603
|
C | A | 11 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(8): Show | 11 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.2914-107C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109206603 | ||||||
| chr12:109206642
|
G | A | 80 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0091others(77): Show | 80 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.2914-68G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | 109206642 | ||||||
| chr12:109206866
|
C | T | 13 | a0001c0002t0001g0035a0001c0012t0002g0045a0001c0012t0002g0250others(10): Show | 13 | HG00673.hp1 HG02040.hp1 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.3060+10C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109206866 | ||||||
| chr12:109207006
|
G | A | 1 | a0032c0059t0002g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3060+150G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109207006 | ||||||
| chr12:109207040
|
C | T | 12 | a0001c0002t0001g0235a0001c0013t0001g0153a0001c0013t0001g0163others(9): Show | 12 | HG00544.hp1 HG00609.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.3060+184C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109207040 | ||||||
| chr12:109207095
|
A | T | 1 | a0018c0051t0023g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3060+239A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109207095 | ||||||
| chr12:109207167
|
G | T | 16 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(13): Show | 16 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.3060+311G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109207167 | ||||||
| chr12:109207226
|
G | A | 5 | a0007c0037t0004g0200a0007c0057t0004g0207a0033c0063t0010g0117others(2): Show | 5 | HG02145.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3060+370G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109207226 | ||||||
| chr12:109207249
|
C | T | 13 | a0001c0002t0001g0035a0001c0012t0002g0045a0001c0012t0002g0250others(10): Show | 13 | HG00673.hp1 HG02040.hp1 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.3060+393C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109207249 | ||||||
| chr12:109207458
|
A | G | 5 | a0001c0003t0004g0074a0002c0017t0003g0042a0017c0123t0015g0058others(2): Show | 5 | HG01081.hp1 HG01884.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3060+602A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109207458 | ||||||
| chr12:109207507
|
C | T | 1 | a0002c0007t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3060+651C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109207507 | ||||||
| chr12:109207580
|
G | C | 19 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(16): Show | 19 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.3060+724G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109207580 | ||||||
| chr12:109208011
|
A | G | 1 | a0001c0002t0001g0085 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3061-1154A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109208011 | ||||||
| chr12:109208217
|
AT | A | 102 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(99): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.3061-932delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | INFO_REALIGN_3_PRIME | chr12 | 109208217 | |||||
| chr12:109208320
|
A | C | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3061-845A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109208320 | ||||||
| chr12:109208320
|
A | G | 1 | a0001c0016t0009g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3061-845A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109208320 | ||||||
| chr12:109208397
|
G | A | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3061-768G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109208397 | ||||||
| chr12:109208455
|
G | A | 1 | a0001c0012t0002g0262 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3061-710G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109208455 | ||||||
| chr12:109208540
|
G | A | 1 | a0001c0062t0019g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3061-625G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109208540 | ||||||
| chr12:109208645
|
C | T | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3061-520C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109208645 | ||||||
| chr12:109208917
|
A | C | 115 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(112): Show | 115 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.3061-248A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109208917 | ||||||
| chr12:109209157
|
C | T | 1 | a0001c0004t0002g0050 | 1 | NA18993.hp2 | splice_region_variant&intron_variant | LOW | c.3061-8C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | chr12 | 109209157 | ||||||
| chr12:109209475
|
A | G | 57 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.3249+122A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209475 | ||||||
| chr12:109209721
|
T | C | 1 | a0002c0014t0003g0106 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3249+368T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209721 | ||||||
| chr12:109209767
|
A | ATG | 7 | a0001c0002t0001g0075a0001c0010t0001g0188a0001c0064t0009g0184others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3249+430_3249+431d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209767 | |||||
| chr12:109209819
|
ATG | A | 5 | a0007c0037t0004g0200a0007c0057t0004g0207a0033c0063t0010g0117others(2): Show | 5 | HG02145.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3249+467_3249+468d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209819 | ||||||
| chr12:109209821
|
G | A | 111 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(108): Show | 111 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.3249+468G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209821 | ||||||
| chr12:109209830
|
T | TACACATA others(27): Show |
1 | a0001c0012t0002g0259 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3249+540_3249+573d others(36): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209830 | |||||
| chr12:109209832
|
C | CACATACA others(19): Show |
10 | a0002c0006t0005g0284a0002c0006t0005g0294a0002c0017t0024g0044others(7): Show | 10 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3249+481_3249+506d others(28): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209832 | |||||
| chr12:109209860
|
T | C | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+507T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209860 | ||||||
| chr12:109209864
|
C | T | 115 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(112): Show | 115 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.3249+511C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209864 | ||||||
| chr12:109209870
|
T | C | 2 | a0001c0011t0001g0013a0012c0035t0004g0082 | 2 | HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.3249+517T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209870 | ||||||
| chr12:109209871
|
ACACACAC others(527): Show |
A | 3 | a0002c0021t0003g0253a0002c0024t0003g0034a0002c0024t0003g0036 | 3 | NA18612.hp1 NA19009.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.3249+526_3249+1059 others(3): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209871 | |||||
| chr12:109209881
|
G | A | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+528G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209881 | ||||||
| chr12:109209885
|
A | G | 1 | a0001c0039t0004g0116 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3249+532A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209885 | ||||||
| chr12:109209893
|
A | G | 16 | a0001c0002t0001g0081a0001c0002t0001g0109a0001c0004t0002g0052others(13): Show | 16 | HG00544.hp2 HG00597.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.3249+540A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209893 | ||||||
| chr12:109209898
|
C | T | 115 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(112): Show | 115 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.3249+545C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209898 | ||||||
| chr12:109209900
|
C | T | 6 | a0001c0013t0001g0248a0003c0001t0001g0140a0003c0001t0001g0141others(3): Show | 6 | NA18945.hp2 NA18961.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.3249+547C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209900 | ||||||
| chr12:109209902
|
C | CACGTGTG others(159): Show |
4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+550_3249+551i others(168): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209902 | |||||
| chr12:109209904
|
T | C | 65 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(62): Show | 65 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.3249+551T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209904 | ||||||
| chr12:109209910
|
C | CATACGT | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+558_3249+559i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209910 | |||||
| chr12:109209910
|
C | CGTGTGTG others(23): Show |
1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3249+557_3249+558i others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209910 | ||||||
| chr12:109209911
|
A | G | 12 | a0001c0002t0001g0191a0001c0013t0001g0248a0002c0006t0014g0080others(9): Show | 12 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.3249+558A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209911 | ||||||
| chr12:109209912
|
C | CGT | 79 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(76): Show | 79 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.3249+564_3249+565d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209912 | |||||
| chr12:109209912
|
C | CGTGTGTA others(25): Show |
1 | a0002c0097t0003g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3249+584_3249+585i others(34): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209912 | |||||
| chr12:109209912
|
C | CGTGTGTA others(23): Show |
2 | a0001c0023t0001g0100a0001c0023t0001g0122 | 2 | HG01515.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3249+584_3249+585i others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209912 | |||||
| chr12:109209912
|
C | CGTGTGTA others(29): Show |
13 | a0001c0002t0001g0085a0001c0002t0001g0098a0001c0012t0002g0262others(10): Show | 13 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.3249+615_3249+650d others(38): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209912 | |||||
| chr12:109209912
|
C | T | 17 | a0001c0002t0001g0191a0001c0013t0001g0248a0002c0006t0014g0080others(14): Show | 17 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.3249+559C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209912 | ||||||
| chr12:109209912
|
CGTGTGTA others(29): Show |
C | 6 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(3): Show | 6 | HG02976.hp1 HG03139.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.3249+615_3249+650d others(38): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209912 | |||||
| chr12:109209913
|
G | A | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3249+560G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209913 | ||||||
| chr12:109209918
|
T | TGTATATA others(41): Show |
1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3249+565_3249+566i others(50): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209918 | ||||||
| chr12:109209919
|
A | G | 2 | a0005c0019t0003g0135a0031c0067t0003g0027 | 2 | HG02015.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3249+566A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209919 | ||||||
| chr12:109209927
|
G | A | 84 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(81): Show | 84 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.3249+574G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209927 | ||||||
| chr12:109209932
|
C | T | 23 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0009g0186others(20): Show | 23 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.3249+579C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209932 | ||||||
| chr12:109209932
|
CACACAT | C | 3 | a0002c0070t0005g0199a0004c0112t0001g0119a0027c0065t0005g0225 | 3 | HG01081.hp1 HG02074.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3249+585_3249+590d others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209932 | |||||
| chr12:109209934
|
C | T | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+581C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209934 | ||||||
| chr12:109209936
|
C | CACATATA others(5): Show |
17 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(14): Show | 17 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.3249+584_3249+585i others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | CACATATA others(381): Show |
1 | a0017c0123t0015g0058 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3249+584_3249+585i others(390): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | CACATATA others(345): Show |
3 | a0002c0017t0003g0042a0006c0113t0004g0031a0026c0066t0015g0115 | 3 | HG02559.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3249+584_3249+585i others(354): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | CACATATA others(281): Show |
1 | a0001c0003t0004g0074 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3249+584_3249+585i others(290): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | CACATATA others(159): Show |
1 | a0001c0002t0001g0235 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3249+584_3249+585i others(168): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | CACATATA others(57): Show |
4 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(1): Show | 4 | HG00280.hp2 HG02723.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.3249+584_3249+585i others(66): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | CACATATA others(133): Show |
4 | a0001c0013t0001g0153a0001c0013t0001g0163a0003c0001t0001g0149others(1): Show | 4 | HG00544.hp1 HG02056.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.3249+584_3249+585i others(142): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | CACATATA others(159): Show |
2 | a0011c0027t0004g0150a0012c0035t0004g0082 | 2 | HG01261.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.3249+584_3249+585i others(168): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | CACATATA others(159): Show |
46 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(43): Show | 46 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.3249+584_3249+585i others(168): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | CACATATA others(157): Show |
1 | a0003c0001t0001g0064 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3249+584_3249+585i others(166): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | CACATATA others(157): Show |
1 | a0003c0001t0004g0266 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3249+584_3249+585i others(166): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | CACATATA others(183): Show |
2 | a0003c0001t0001g0158a0003c0001t0001g0265 | 2 | HG02040.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.3249+584_3249+585i others(192): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | CACATATA others(55): Show |
1 | a0002c0061t0003g0062 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3249+584_3249+585i others(64): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | CACATATA others(157): Show |
1 | a0001c0003t0002g0099 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3249+584_3249+585i others(166): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209936
|
C | T | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+583C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209936 | ||||||
| chr12:109209936
|
CAT | C | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+585_3249+586d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209936 | |||||
| chr12:109209938
|
T | C | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+585T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209938 | ||||||
| chr12:109209940
|
C | T | 5 | a0001c0003t0004g0074a0002c0017t0003g0042a0006c0113t0004g0031others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3249+587C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209940 | ||||||
| chr12:109209942
|
C | T | 4 | a0001c0016t0011g0274a0006c0026t0002g0155a0006c0026t0002g0156others(1): Show | 4 | HG00323.hp1 HG02523.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3249+589C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209942 | ||||||
| chr12:109209943
|
A | G | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3249+590A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209943 | ||||||
| chr12:109209944
|
C | CGT | 58 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(55): Show | 58 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.3249+591_3249+592i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209944 | ||||||
| chr12:109209944
|
C | T | 7 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(4): Show | 7 | HG00323.hp1 HG01069.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.3249+591C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209944 | ||||||
| chr12:109209945
|
A | ATACATG | 6 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(3): Show | 6 | HG00280.hp2 HG02723.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.3249+592_3249+593i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209945 | ||||||
| chr12:109209946
|
C | CAT | 15 | a0001c0039t0004g0116a0001c0069t0002g0204a0001c0074t0004g0229others(12): Show | 15 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3249+593_3249+594i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209946 | ||||||
| chr12:109209946
|
C | T | 8 | a0002c0070t0005g0199a0004c0112t0001g0119a0006c0026t0002g0155others(5): Show | 8 | HG00323.hp1 HG01081.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.3249+593C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209946 | ||||||
| chr12:109209946
|
CGT | C | 4 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169others(1): Show | 4 | HG02280.hp2 HG02559.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+600_3249+601d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209946 | |||||
| chr12:109209947
|
G | A | 25 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(22): Show | 25 | HG00280.hp2 HG01081.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.3249+594G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209947 | ||||||
| chr12:109209947
|
G | GTA | 62 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(59): Show | 62 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.3249+595_3249+596i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209947 | |||||
| chr12:109209949
|
G | A | 19 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(16): Show | 19 | HG01081.hp1 HG01891.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.3249+596G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209949 | ||||||
| chr12:109209951
|
G | A | 4 | a0001c0039t0004g0039a0006c0026t0002g0155a0006c0026t0002g0156others(1): Show | 4 | HG00323.hp1 HG02523.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3249+598G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209951 | ||||||
| chr12:109209952
|
T | TACACAC | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+599_3249+600i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209952 | ||||||
| chr12:109209953
|
G | A | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+600G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209953 | ||||||
| chr12:109209954
|
T | C | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+601T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209954 | ||||||
| chr12:109209955
|
A | G | 1 | a0001c0039t0004g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3249+602A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209955 | ||||||
| chr12:109209959
|
A | ATACACAC others(51): Show |
12 | a0001c0039t0004g0116a0001c0074t0004g0229a0001c0095t0001g0133others(9): Show | 12 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3249+607_3249+608i others(60): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209959 | |||||
| chr12:109209959
|
A | ATACACAC others(75): Show |
3 | a0001c0069t0002g0204a0001c0124t0012g0197a0002c0092t0010g0192 | 3 | HG03579.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3249+607_3249+608i others(84): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209959 | |||||
| chr12:109209963
|
G | A | 24 | a0001c0039t0004g0116a0001c0064t0009g0184a0001c0069t0002g0204others(21): Show | 24 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.3249+610G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209963 | ||||||
| chr12:109209967
|
A | ATG | 5 | a0001c0003t0004g0074a0002c0017t0003g0042a0006c0113t0004g0031others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3249+614_3249+615i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209967 | ||||||
| chr12:109209968
|
C | T | 101 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(98): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.3249+615C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209968 | ||||||
| chr12:109209969
|
A | G | 5 | a0001c0003t0004g0074a0002c0017t0003g0042a0006c0113t0004g0031others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3249+616A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209969 | ||||||
| chr12:109209970
|
C | T | 75 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(72): Show | 75 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.3249+617C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209970 | ||||||
| chr12:109209972
|
C | CACACATA others(321): Show |
1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3249+620_3249+621i others(330): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209972 | |||||
| chr12:109209972
|
C | CACACATA others(261): Show |
1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3249+620_3249+621i others(270): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209972 | |||||
| chr12:109209972
|
C | CACATATA others(241): Show |
2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3249+620_3249+621i others(250): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209972 | |||||
| chr12:109209972
|
C | CACATATA others(429): Show |
4 | a0001c0016t0009g0287a0001c0032t0004g0291a0001c0032t0004g0292others(1): Show | 4 | HG02258.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+620_3249+621i others(438): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209972 | |||||
| chr12:109209972
|
C | CACATATA others(455): Show |
2 | a0001c0010t0009g0186a0001c0016t0009g0290 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3249+620_3249+621i others(464): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209972 | |||||
| chr12:109209972
|
C | CACATATA others(393): Show |
2 | a0001c0016t0009g0305a0001c0106t0001g0293 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3249+620_3249+621i others(402): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209972 | |||||
| chr12:109209972
|
C | CACATATG others(315): Show |
1 | a0027c0065t0005g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3249+620_3249+621i others(324): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209972 | |||||
| chr12:109209972
|
C | CATATGTG others(331): Show |
1 | a0004c0112t0001g0119 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3249+622_3249+623i others(340): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209972 | |||||
| chr12:109209972
|
C | T | 20 | a0001c0003t0004g0074a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+619C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209972 | ||||||
| chr12:109209972
|
CAT | C | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+621_3249+622d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209972 | |||||
| chr12:109209974
|
T | C | 68 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(65): Show | 68 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.3249+621T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209974 | ||||||
| chr12:109209976
|
C | CACACACG others(333): Show |
1 | a0036c0094t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3249+650_3249+651i others(342): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209976 | |||||
| chr12:109209976
|
C | CACACACG others(421): Show |
3 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3249+650_3249+651i others(430): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209976 | |||||
| chr12:109209976
|
C | T | 21 | a0001c0003t0004g0074a0001c0010t0009g0186a0001c0016t0009g0287others(18): Show | 21 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.3249+623C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209976 | ||||||
| chr12:109209978
|
C | T | 71 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(68): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.3249+625C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209978 | ||||||
| chr12:109209979
|
A | G | 2 | a0001c0039t0004g0039a0002c0070t0005g0199 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3249+626A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209979 | ||||||
| chr12:109209980
|
C | T | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+627C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209980 | ||||||
| chr12:109209981
|
A | ATG | 6 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(3): Show | 6 | HG00280.hp2 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3249+628_3249+629i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209981 | ||||||
| chr12:109209981
|
A | G | 5 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(2): Show | 5 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.3249+628A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209981 | ||||||
| chr12:109209982
|
C | T | 65 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(62): Show | 65 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.3249+629C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209982 | ||||||
| chr12:109209983
|
G | A | 71 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.3249+630G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209983 | ||||||
| chr12:109209985
|
G | A | 2 | a0001c0039t0004g0039a0002c0070t0005g0199 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3249+632G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209985 | ||||||
| chr12:109209985
|
G | GTATA | 15 | a0001c0039t0004g0116a0001c0069t0002g0204a0001c0074t0004g0229others(12): Show | 15 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3249+633_3249+634i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209985 | |||||
| chr12:109209986
|
T | C | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+633T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209986 | ||||||
| chr12:109209987
|
G | A | 18 | a0001c0039t0004g0116a0001c0069t0002g0204a0001c0074t0004g0229others(15): Show | 18 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3249+634G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209987 | ||||||
| chr12:109209995
|
A | ACACACAT others(45): Show |
1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3249+642_3249+643i others(54): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209995 | ||||||
| chr12:109209995
|
A | ATGTATAT others(207): Show |
1 | a0033c0063t0010g0117 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3249+645_3249+646i others(216): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209995 | |||||
| chr12:109209995
|
A | ATGTATAT others(243): Show |
2 | a0007c0057t0004g0207a0039c0080t0010g0071 | 2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3249+645_3249+646i others(252): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209995 | |||||
| chr12:109209995
|
A | ATGTATAT others(179): Show |
1 | a0007c0037t0004g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3249+645_3249+646i others(188): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209995 | |||||
| chr12:109209995
|
A | ATGTATAT others(243): Show |
1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3249+645_3249+646i others(252): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109209995 | |||||
| chr12:109209997
|
G | A | 15 | a0001c0039t0004g0116a0001c0069t0002g0204a0001c0074t0004g0229others(12): Show | 15 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3249+644G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209997 | ||||||
| chr12:109209998
|
T | C | 15 | a0001c0039t0004g0116a0001c0069t0002g0204a0001c0074t0004g0229others(12): Show | 15 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3249+645T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209998 | ||||||
| chr12:109209999
|
G | A | 22 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.3249+646G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109209999 | ||||||
| chr12:109210000
|
T | C | 15 | a0001c0039t0004g0116a0001c0069t0002g0204a0001c0074t0004g0229others(12): Show | 15 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3249+647T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210000 | ||||||
| chr12:109210000
|
T | TATATATG others(191): Show |
1 | a0003c0001t0001g0149 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3249+651_3249+652i others(200): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210000 | |||||
| chr12:109210003
|
A | ATATACAC others(11): Show |
4 | a0001c0010t0001g0188a0001c0013t0001g0256a0002c0061t0003g0062others(1): Show | 4 | HG00280.hp2 HG02723.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.3249+651_3249+652i others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210003 | |||||
| chr12:109210003
|
A | ATATACAC others(37): Show |
1 | a0001c0011t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3249+651_3249+652i others(46): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210003 | |||||
| chr12:109210004
|
T | TACGTATA others(7): Show |
1 | a0002c0070t0005g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3249+651_3249+652i others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210004 | ||||||
| chr12:109210005
|
G | A | 82 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(79): Show | 82 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.3249+652G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210005 | ||||||
| chr12:109210006
|
T | C | 1 | a0001c0039t0004g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3249+653T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210006 | ||||||
| chr12:109210009
|
A | ATATATAC others(1): Show |
61 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.3249+663_3249+664i others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210009 | |||||
| chr12:109210009
|
A | G | 15 | a0001c0039t0004g0116a0001c0069t0002g0204a0001c0074t0004g0229others(12): Show | 15 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3249+656A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210009 | ||||||
| chr12:109210014
|
T | TACGTATA others(3): Show |
2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3249+663_3249+664i others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210014 | |||||
| chr12:109210014
|
TACAC | T | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+664_3249+667d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210014 | |||||
| chr12:109210021
|
G | A | 5 | a0001c0016t0011g0274a0002c0070t0005g0199a0007c0037t0004g0200others(2): Show | 5 | HG02145.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.3249+668G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210021 | ||||||
| chr12:109210021
|
G | GTACATA | 15 | a0001c0039t0004g0116a0001c0069t0002g0204a0001c0074t0004g0229others(12): Show | 15 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3249+669_3249+670i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210021 | |||||
| chr12:109210022
|
T | C | 1 | a0002c0070t0005g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3249+669T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210022 | ||||||
| chr12:109210023
|
G | A | 12 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(9): Show | 12 | HG00280.hp2 HG00323.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.3249+670G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210023 | ||||||
| chr12:109210024
|
T | C | 9 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(6): Show | 9 | HG00280.hp2 HG02145.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3249+671T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210024 | ||||||
| chr12:109210024
|
T | TATATATA others(57): Show |
2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3249+671_3249+672i others(66): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210024 | ||||||
| chr12:109210025
|
G | A | 8 | a0001c0039t0004g0039a0006c0026t0002g0155a0006c0026t0002g0156others(5): Show | 8 | HG00323.hp1 HG01069.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.3249+672G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210025 | ||||||
| chr12:109210027
|
A | G | 2 | a0017c0123t0015g0058a0026c0066t0015g0115 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.3249+674A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210027 | ||||||
| chr12:109210028
|
T | C | 5 | a0001c0002t0001g0282a0001c0002t0001g0283a0006c0026t0002g0155others(2): Show | 5 | HG00323.hp1 HG02523.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.3249+675T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210028 | ||||||
| chr12:109210029
|
A | G | 9 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(6): Show | 9 | HG00280.hp2 HG02145.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3249+676A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210029 | ||||||
| chr12:109210030
|
T | C | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+677T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210030 | ||||||
| chr12:109210030
|
T | TACACGTA others(27): Show |
2 | a0003c0001t0001g0136a0003c0001t0001g0137 | 2 | HG00609.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3249+678_3249+679i others(36): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210030 | |||||
| chr12:109210030
|
T | TACATATA others(5): Show |
1 | a0001c0039t0004g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3249+678_3249+679i others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210030 | |||||
| chr12:109210031
|
A | ACGTATAT others(59): Show |
4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+678_3249+679i others(68): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210031 | ||||||
| chr12:109210031
|
A | G | 9 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(6): Show | 9 | HG00280.hp2 HG02145.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3249+678A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210031 | ||||||
| chr12:109210032
|
T | C | 40 | a0001c0002t0001g0191a0001c0002t0001g0235a0001c0003t0002g0099others(37): Show | 40 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.3249+679T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210032 | ||||||
| chr12:109210034
|
T | TATATATA others(3): Show |
1 | a0002c0070t0005g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3249+681_3249+682i others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210034 | ||||||
| chr12:109210035
|
G | A | 71 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(68): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.3249+682G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210035 | ||||||
| chr12:109210036
|
T | C | 2 | a0003c0001t0001g0136a0003c0001t0001g0137 | 2 | HG00609.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3249+683T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210036 | ||||||
| chr12:109210036
|
T | TATACACA others(51): Show |
1 | a0001c0011t0001g0008 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3249+686_3249+687i others(60): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210036
|
T | TATACACA others(75): Show |
19 | a0001c0002t0001g0191a0001c0002t0001g0235a0001c0003t0002g0099others(16): Show | 19 | HG00423.hp2 HG00597.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.3249+686_3249+687i others(84): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210036
|
T | TATACACA others(99): Show |
2 | a0003c0001t0001g0087a0011c0027t0004g0249 | 2 | NA18966.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.3249+686_3249+687i others(108): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210036
|
T | TATACACA others(123): Show |
2 | a0003c0005t0002g0134a0005c0009t0006g0257 | 2 | NA18747.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.3249+686_3249+687i others(132): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210036
|
T | TATACACA others(147): Show |
9 | a0001c0013t0001g0153a0001c0013t0001g0163a0001c0013t0001g0248others(6): Show | 9 | HG00544.hp1 NA18945.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.3249+686_3249+687i others(156): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210036
|
T | TATACACA others(195): Show |
1 | a0003c0001t0001g0147 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3249+686_3249+687i others(204): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210036
|
T | TATATACA others(7): Show |
14 | a0001c0039t0004g0116a0001c0069t0002g0204a0001c0074t0004g0229others(11): Show | 14 | HG01891.hp1 HG02257.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.3249+687_3249+688i others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210036
|
T | TATATACG others(85): Show |
2 | a0001c0002t0001g0075a0011c0027t0013g0065 | 2 | HG01168.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.3249+687_3249+688i others(94): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210036
|
T | TATATACG others(109): Show |
2 | a0001c0002t0001g0079a0001c0002t0001g0091 | 2 | HG00741.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.3249+687_3249+688i others(118): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210036
|
T | TATATACG others(133): Show |
2 | a0001c0023t0004g0121a0002c0043t0003g0012 | 2 | HG00735.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.3249+687_3249+688i others(142): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210036
|
T | TATATACG others(157): Show |
6 | a0002c0006t0005g0123a0002c0024t0003g0302a0002c0086t0003g0260others(3): Show | 6 | HG00741.hp2 HG01255.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.3249+687_3249+688i others(166): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210036
|
T | TATATACG others(181): Show |
7 | a0001c0002t0001g0035a0003c0001t0001g0064a0003c0001t0001g0138others(4): Show | 7 | HG00642.hp2 HG01069.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.3249+687_3249+688i others(190): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210036
|
T | TATATACG others(205): Show |
1 | a0011c0027t0004g0150 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3249+687_3249+688i others(214): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210036
|
T | TATATACG others(239): Show |
1 | a0003c0001t0004g0266 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3249+687_3249+688i others(248): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210036 | |||||
| chr12:109210038
|
T | TATACACA others(5): Show |
1 | a0030c0071t0002g0040 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3249+687_3249+688i others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210038 | |||||
| chr12:109210039
|
ATG | A | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+690_3249+691d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210039 | |||||
| chr12:109210041
|
G | A | 9 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0039t0004g0039others(6): Show | 9 | HG02074.hp2 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.3249+688G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210041 | ||||||
| chr12:109210043
|
G | A | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+690G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210043 | ||||||
| chr12:109210045
|
A | G | 3 | a0001c0002t0001g0282a0001c0002t0001g0283a0030c0071t0002g0040 | 3 | HG02615.hp1 HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3249+692A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210045 | ||||||
| chr12:109210046
|
T | C | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+693T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210046 | ||||||
| chr12:109210050
|
T | C | 1 | a0002c0070t0005g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3249+697T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210050 | ||||||
| chr12:109210052
|
C | T | 1 | a0030c0071t0002g0040 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3249+699C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210052 | ||||||
| chr12:109210056
|
C | CATACAT | 5 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(2): Show | 5 | HG00280.hp2 HG02723.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.3249+704_3249+705i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210056 | |||||
| chr12:109210056
|
C | CATACGT | 3 | a0007c0037t0004g0200a0033c0063t0010g0117a0035c0076t0010g0267 | 3 | HG02145.hp2 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3249+704_3249+705i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210056 | |||||
| chr12:109210056
|
C | T | 1 | a0001c0039t0004g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3249+703C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210056 | ||||||
| chr12:109210057
|
A | ATACGTAT others(197): Show |
1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3249+704_3249+705i others(206): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210057 | ||||||
| chr12:109210057
|
A | G | 77 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(74): Show | 77 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.3249+704A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210057 | ||||||
| chr12:109210058
|
C | T | 88 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(85): Show | 88 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.3249+705C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210058 | ||||||
| chr12:109210059
|
G | A | 2 | a0001c0039t0004g0039a0002c0070t0005g0199 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3249+706G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210059 | ||||||
| chr12:109210061
|
G | GTATATA | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+709_3249+710i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210061 | |||||
| chr12:109210063
|
G | A | 2 | a0007c0057t0004g0207a0039c0080t0010g0071 | 2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3249+710G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210063 | ||||||
| chr12:109210065
|
A | G | 13 | a0001c0012t0002g0259a0001c0039t0004g0116a0001c0074t0004g0229others(10): Show | 13 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.3249+712A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210065 | ||||||
| chr12:109210066
|
T | TATACACA others(5): Show |
1 | a0001c0039t0004g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3249+716_3249+717i others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210066 | |||||
| chr12:109210066
|
T | TATACGTA others(55): Show |
2 | a0007c0057t0004g0207a0039c0080t0010g0071 | 2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3249+716_3249+717i others(64): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210066 | |||||
| chr12:109210069
|
A | G | 1 | a0001c0012t0002g0259 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3249+716A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210069 | ||||||
| chr12:109210071
|
G | A | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+718G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210071 | ||||||
| chr12:109210072
|
T | C | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+719T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210072 | ||||||
| chr12:109210073
|
G | A | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+720G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210073 | ||||||
| chr12:109210074
|
T | C | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+721T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210074 | ||||||
| chr12:109210077
|
A | G | 6 | a0001c0018t0002g0048a0001c0018t0002g0049a0001c0018t0011g0046others(3): Show | 6 | HG01070.hp2 HG01123.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.3249+724A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210077 | ||||||
| chr12:109210079
|
A | ACACACGT others(7): Show |
1 | a0002c0070t0005g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3249+726_3249+727i others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210079 | ||||||
| chr12:109210079
|
A | G | 93 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(90): Show | 93 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.3249+726A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210079 | ||||||
| chr12:109210083
|
A | G | 6 | a0001c0039t0004g0039a0006c0026t0002g0155a0006c0026t0002g0156others(3): Show | 6 | HG00323.hp1 HG02523.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.3249+730A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210083 | ||||||
| chr12:109210088
|
T | C | 2 | a0003c0001t0001g0149a0004c0112t0001g0119 | 2 | HG02056.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.3249+735T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210088 | ||||||
| chr12:109210089
|
A | ACGTATAT others(73): Show |
3 | a0007c0037t0004g0200a0033c0063t0010g0117a0035c0076t0010g0267 | 3 | HG02145.hp2 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3249+737_3249+738i others(82): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210089 | |||||
| chr12:109210090
|
C | CGTATAT | 5 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(2): Show | 5 | HG00280.hp2 HG02723.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.3249+737_3249+738i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210090 | ||||||
| chr12:109210090
|
C | T | 2 | a0007c0057t0004g0207a0039c0080t0010g0071 | 2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3249+737C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210090 | ||||||
| chr12:109210094
|
C | CACGTGTG others(3): Show |
1 | a0036c0094t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3249+742_3249+743i others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210094 | |||||
| chr12:109210094
|
C | CGTACAT | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+741_3249+742i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210094 | ||||||
| chr12:109210094
|
C | CGTGTGTA others(1): Show |
11 | a0001c0016t0011g0274a0001c0069t0002g0204a0001c0074t0004g0229others(8): Show | 11 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.3249+741_3249+742i others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210094 | ||||||
| chr12:109210094
|
C | T | 3 | a0007c0037t0004g0200a0033c0063t0010g0117a0035c0076t0010g0267 | 3 | HG02145.hp2 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3249+741C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210094 | ||||||
| chr12:109210095
|
A | C | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3249+742A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210095 | ||||||
| chr12:109210095
|
A | G | 72 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.3249+742A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210095 | ||||||
| chr12:109210095
|
ATG | A | 3 | a0002c0053t0005g0033a0004c0040t0002g0213a0005c0056t0003g0053 | 3 | HG03831.hp2 HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3249+750_3249+751d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210095 | |||||
| chr12:109210096
|
T | C | 16 | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0011t0001g0013others(13): Show | 16 | HG00280.hp2 HG00408.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3249+743T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210096 | ||||||
| chr12:109210097
|
G | A | 13 | a0001c0016t0011g0274a0001c0069t0002g0204a0001c0074t0004g0229others(10): Show | 13 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.3249+744G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210097 | ||||||
| chr12:109210099
|
G | GTATATA | 59 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(56): Show | 59 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.3249+747_3249+748i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210099 | |||||
| chr12:109210101
|
G | A | 17 | a0001c0011t0001g0008a0001c0039t0004g0039a0001c0039t0004g0116others(14): Show | 17 | HG00323.hp1 HG00323.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.3249+748G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210101 | ||||||
| chr12:109210102
|
T | C | 1 | a0001c0039t0004g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3249+749T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210102 | ||||||
| chr12:109210103
|
G | A | 34 | a0001c0010t0001g0188a0001c0011t0001g0008a0001c0011t0001g0013others(31): Show | 34 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.3249+750G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210103 | ||||||
| chr12:109210105
|
A | G | 1 | a0010c0075t0003g0214 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3249+752A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210105 | ||||||
| chr12:109210107
|
A | ATATGTGT others(5): Show |
2 | a0007c0057t0004g0207a0039c0080t0010g0071 | 2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3249+755_3249+756i others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210107 | |||||
| chr12:109210107
|
A | G | 21 | a0001c0011t0001g0008a0001c0039t0004g0039a0001c0039t0004g0116others(18): Show | 21 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.3249+754A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210107 | ||||||
| chr12:109210109
|
G | A | 57 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(54): Show | 57 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.3249+756G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210109 | ||||||
| chr12:109210109
|
G | GTGTATAT others(5): Show |
1 | a0002c0070t0005g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3249+757_3249+758i others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210109 | |||||
| chr12:109210111
|
A | G | 58 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(55): Show | 58 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3249+758A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210111 | ||||||
| chr12:109210116
|
T | C | 4 | a0002c0070t0005g0199a0006c0026t0002g0155a0006c0026t0002g0156others(1): Show | 4 | HG00323.hp1 HG02523.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3249+763T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210116 | ||||||
| chr12:109210116
|
T | TAC | 6 | a0001c0069t0002g0204a0001c0074t0004g0229a0001c0124t0012g0197others(3): Show | 6 | HG01891.hp1 HG02056.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.3249+766_3249+767d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210116 | |||||
| chr12:109210116
|
T | TACGTATA others(183): Show |
1 | a0019c0093t0001g0159 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3249+765_3249+766i others(192): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210116 | |||||
| chr12:109210117
|
A | G | 10 | a0001c0011t0001g0008a0001c0039t0004g0116a0001c0095t0001g0133others(7): Show | 10 | HG00323.hp2 HG02257.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3249+764A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210117 | ||||||
| chr12:109210118
|
C | CGT | 4 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(1): Show | 4 | HG00280.hp2 HG02723.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.3249+765_3249+766i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210118 | ||||||
| chr12:109210118
|
C | T | 10 | a0001c0011t0001g0008a0001c0039t0004g0116a0001c0095t0001g0133others(7): Show | 10 | HG00323.hp2 HG02257.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3249+765C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210118 | ||||||
| chr12:109210120
|
C | T | 15 | a0001c0010t0001g0188a0001c0011t0001g0008a0001c0011t0001g0013others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.3249+767C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210120 | ||||||
| chr12:109210121
|
G | A | 78 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(75): Show | 78 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.3249+768G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210121 | ||||||
| chr12:109210122
|
T | C | 64 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(61): Show | 64 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.3249+769T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210122 | ||||||
| chr12:109210123
|
A | G | 15 | a0001c0039t0004g0039a0001c0069t0002g0204a0001c0074t0004g0229others(12): Show | 15 | HG01891.hp1 HG02056.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.3249+770A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210123 | ||||||
| chr12:109210124
|
C | T | 25 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(22): Show | 25 | HG01891.hp1 HG02056.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.3249+771C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210124 | ||||||
| chr12:109210124
|
CATGTATG others(5): Show |
C | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+774_3249+785d others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210124 | |||||
| chr12:109210125
|
A | ACACGTGT others(97): Show |
2 | a0001c0010t0001g0188a0001c0013t0001g0256 | 2 | HG00280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.3249+772_3249+773i others(106): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210125 | ||||||
| chr12:109210125
|
A | ACACGTGT others(121): Show |
1 | a0001c0011t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3249+772_3249+773i others(130): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210125 | ||||||
| chr12:109210125
|
A | ACACGTGT others(169): Show |
1 | a0002c0061t0003g0062 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3249+772_3249+773i others(178): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210125 | ||||||
| chr12:109210125
|
A | G | 79 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(76): Show | 79 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.3249+772A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210125 | ||||||
| chr12:109210126
|
T | C | 10 | a0001c0011t0001g0008a0001c0039t0004g0116a0001c0095t0001g0133others(7): Show | 10 | HG00323.hp2 HG02257.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3249+773T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210126 | ||||||
| chr12:109210127
|
G | A | 25 | a0001c0010t0001g0188a0001c0011t0001g0008a0001c0011t0001g0013others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.3249+774G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210127 | ||||||
| chr12:109210127
|
G | GTA | 3 | a0002c0024t0003g0302a0003c0001t0001g0143a0004c0008t0001g0221 | 3 | HG00642.hp2 HG00741.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.3249+776_3249+777d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210127 | |||||
| chr12:109210127
|
G | GTGTA | 64 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(61): Show | 64 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.3249+775_3249+776i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210127 | |||||
| chr12:109210128
|
T | C | 10 | a0001c0011t0001g0008a0001c0039t0004g0116a0001c0095t0001g0133others(7): Show | 10 | HG00323.hp2 HG02257.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3249+775T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210128 | ||||||
| chr12:109210130
|
T | C | 12 | a0001c0011t0001g0008a0001c0039t0004g0116a0001c0095t0001g0133others(9): Show | 12 | HG00323.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3249+777T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210130 | ||||||
| chr12:109210131
|
G | A | 83 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(80): Show | 83 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.3249+778G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210131 | ||||||
| chr12:109210133
|
G | GTGTATAT others(23): Show |
3 | a0003c0001t0001g0145a0006c0078t0001g0181a0008c0044t0003g0182 | 3 | NA18992.hp2 NA19060.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3249+801_3249+802i others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210133 | |||||
| chr12:109210141
|
A | ATG | 14 | a0001c0003t0004g0074a0001c0010t0009g0186a0001c0016t0009g0287others(11): Show | 14 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3249+790_3249+791d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210141 | |||||
| chr12:109210141
|
A | G | 17 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0001g0188others(14): Show | 17 | HG00280.hp2 HG00323.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.3249+788A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210141 | ||||||
| chr12:109210143
|
G | GTA | 3 | a0007c0037t0004g0200a0033c0063t0010g0117a0035c0076t0010g0267 | 3 | HG02145.hp2 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3249+797_3249+798d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210143 | |||||
| chr12:109210143
|
GTATATAT others(23): Show |
G | 4 | a0002c0017t0003g0042a0017c0123t0015g0058a0026c0066t0015g0115others(1): Show | 4 | HG01081.hp1 HG01884.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+792_3249+821d others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210143 | |||||
| chr12:109210150
|
T | C | 5 | a0001c0002t0001g0075a0002c0006t0005g0123a0011c0027t0013g0065others(2): Show | 5 | HG01168.hp2 HG02257.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3249+797T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210150 | ||||||
| chr12:109210150
|
T | TAC | 9 | a0001c0069t0002g0204a0001c0074t0004g0229a0001c0124t0012g0197others(6): Show | 9 | HG01192.hp2 HG01891.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.3249+802_3249+803d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210150 | |||||
| chr12:109210157
|
G | A | 8 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0016t0011g0274others(5): Show | 8 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.3249+804G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210157 | ||||||
| chr12:109210158
|
T | C | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3249+805T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210158 | ||||||
| chr12:109210161
|
G | A | 1 | a0036c0094t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3249+808G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210161 | ||||||
| chr12:109210161
|
G | GTGTGTA | 3 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066 | 3 | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+809_3249+810i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210161 | |||||
| chr12:109210161
|
GTATA | G | 8 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0016t0011g0274others(5): Show | 8 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.3249+810_3249+813d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210161 | |||||
| chr12:109210163
|
A | G | 1 | a0036c0094t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3249+810A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210163 | ||||||
| chr12:109210165
|
A | ATATG | 84 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(81): Show | 84 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.3249+813_3249+814i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210165 | |||||
| chr12:109210165
|
A | ATATGTAT others(41): Show |
1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3249+813_3249+814i others(50): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210165 | |||||
| chr12:109210165
|
A | ATATGTGT others(7): Show |
1 | a0001c0039t0004g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3249+813_3249+814i others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210165 | |||||
| chr12:109210165
|
A | G | 4 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(1): Show | 4 | HG00323.hp1 HG02523.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+812A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210165 | ||||||
| chr12:109210169
|
A | G | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3249+816A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210169 | ||||||
| chr12:109210173
|
A | G | 6 | a0006c0026t0002g0155a0006c0026t0002g0156a0006c0026t0016g0066others(3): Show | 6 | HG00323.hp1 HG02145.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.3249+820A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210173 | ||||||
| chr12:109210175
|
GTA | G | 3 | a0001c0011t0001g0157a0001c0055t0001g0226a0014c0079t0004g0180 | 3 | HG01433.hp1 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3249+829_3249+830d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210175 | |||||
| chr12:109210182
|
T | C | 7 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(4): Show | 7 | HG00280.hp2 HG01074.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3249+829T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210182 | ||||||
| chr12:109210182
|
T | TAC | 23 | a0001c0002t0001g0085a0001c0039t0004g0039a0001c0039t0004g0116others(20): Show | 23 | HG00099.hp2 HG01192.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.3249+834_3249+835d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210182 | |||||
| chr12:109210186
|
C | CGT | 7 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0016t0011g0274others(4): Show | 7 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3249+833_3249+834i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210186 | ||||||
| chr12:109210186
|
CACGTGTG others(55): Show |
C | 1 | a0008c0015t0005g0057 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3249+836_3249+897d others(64): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210186 | |||||
| chr12:109210187
|
A | G | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3249+834A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210187 | ||||||
| chr12:109210188
|
C | CAT | 14 | a0001c0002t0001g0114a0001c0002t0001g0126a0001c0002t0021g0243others(11): Show | 14 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.3249+835_3249+836i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210188 | ||||||
| chr12:109210188
|
C | T | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3249+835C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210188 | ||||||
| chr12:109210188
|
CGTGTGT | C | 63 | a0001c0002t0001g0081a0001c0002t0001g0109a0001c0002t0001g0241others(60): Show | 63 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.3249+836_3249+841d others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210188 | ||||||
| chr12:109210188
|
CGTGTGTA others(33): Show |
C | 1 | a0003c0081t0002g0230 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3249+836_3249+875d others(42): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210188 | ||||||
| chr12:109210189
|
G | A | 11 | a0001c0002t0001g0098a0001c0002t0001g0282a0001c0002t0001g0283others(8): Show | 11 | HG01069.hp1 HG01074.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.3249+836G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210189 | ||||||
| chr12:109210190
|
T | C | 2 | a0001c0002t0001g0098a0009c0096t0009g0295 | 2 | HG01081.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3249+837T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210190 | ||||||
| chr12:109210191
|
G | A | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3249+838G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210191 | ||||||
| chr12:109210193
|
G | A | 7 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0016t0011g0274others(4): Show | 7 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3249+840G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210193 | ||||||
| chr12:109210193
|
GTATA | G | 59 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(56): Show | 59 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.3249+842_3249+845d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210193 | |||||
| chr12:109210195
|
A | G | 7 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0016t0011g0274others(4): Show | 7 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3249+842A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210195 | ||||||
| chr12:109210196
|
TATGTATA others(13): Show |
T | 3 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3249+845_3249+864d others(22): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210196 | |||||
| chr12:109210197
|
A | ATATG | 27 | a0001c0011t0001g0013a0001c0013t0001g0256a0001c0039t0004g0039others(24): Show | 27 | HG00280.hp2 HG00323.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.3249+845_3249+846i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210197 | |||||
| chr12:109210197
|
A | ATATGTAT others(21): Show |
2 | a0007c0057t0004g0207a0039c0080t0010g0071 | 2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3249+845_3249+846i others(30): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210197 | |||||
| chr12:109210197
|
A | G | 71 | a0001c0002t0001g0081a0001c0002t0001g0109a0001c0002t0001g0241others(68): Show | 71 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.3249+844A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210197 | ||||||
| chr12:109210201
|
A | ATATATAC others(11): Show |
1 | a0001c0111t0001g0275 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3249+853_3249+854i others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210201 | |||||
| chr12:109210201
|
A | ATATATAC others(63): Show |
1 | a0002c0024t0003g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3249+853_3249+854i others(72): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210201 | |||||
| chr12:109210201
|
A | ATATATAC others(11): Show |
18 | a0001c0002t0001g0114a0001c0002t0021g0243a0001c0003t0002g0094others(15): Show | 18 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.3249+853_3249+854i others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210201 | |||||
| chr12:109210201
|
A | ATATATAC others(9): Show |
2 | a0001c0002t0001g0126a0001c0023t0001g0089 | 2 | HG01123.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.3249+853_3249+854i others(18): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210201 | |||||
| chr12:109210201
|
A | G | 66 | a0001c0002t0001g0081a0001c0002t0001g0109a0001c0002t0001g0241others(63): Show | 66 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.3249+848A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210201 | ||||||
| chr12:109210205
|
A | ATACACAC others(3): Show |
1 | a0001c0108t0001g0010 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3249+853_3249+854i others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210205 | |||||
| chr12:109210205
|
A | ATG | 7 | a0001c0016t0011g0274a0007c0057t0004g0207a0009c0025t0001g0105others(4): Show | 7 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3249+854_3249+855d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210205 | |||||
| chr12:109210206
|
TGTATATA others(63): Show |
T | 1 | a0001c0106t0001g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3249+854_3249+923d others(72): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210206 | ||||||
| chr12:109210207
|
G | A | 1 | a0001c0010t0001g0188 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3249+854G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210207 | ||||||
| chr12:109210207
|
GTA | G | 5 | a0001c0023t0001g0100a0001c0023t0001g0122a0002c0007t0003g0026others(2): Show | 5 | HG01258.hp1 HG01515.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.3249+861_3249+862d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210207 | |||||
| chr12:109210209
|
A | G | 3 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0001g0188 | 3 | HG02615.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.3249+856A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210209 | ||||||
| chr12:109210210
|
T | C | 6 | a0001c0011t0001g0056a0001c0054t0001g0203a0002c0007t0003g0037others(3): Show | 6 | HG01884.hp2 HG01943.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3249+857T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210210 | ||||||
| chr12:109210216
|
C | T | 3 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0108t0001g0010 | 3 | HG02615.hp2 HG02630.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3249+863C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210216 | ||||||
| chr12:109210220
|
CAT | C | 63 | a0001c0002t0008g0306a0001c0004t0002g0050a0001c0004t0002g0052others(60): Show | 64 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.3249+868_3249+869d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210220 | ||||||
| chr12:109210221
|
A | G | 67 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(64): Show | 67 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.3249+868A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210221 | ||||||
| chr12:109210222
|
T | C | 38 | a0001c0002t0001g0085a0001c0002t0001g0098a0001c0002t0001g0282others(35): Show | 38 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.3249+869T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210222 | ||||||
| chr12:109210222
|
TGTGTGTA others(23): Show |
T | 1 | a0001c0003t0002g0078 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3249+870_3249+899d others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210222 | ||||||
| chr12:109210223
|
G | A | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3249+870G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210223 | ||||||
| chr12:109210225
|
G | A | 2 | a0003c0001t0001g0149a0009c0096t0009g0295 | 2 | HG02056.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3249+872G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210225 | ||||||
| chr12:109210225
|
G | C | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3249+872G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210225 | ||||||
| chr12:109210225
|
GTGTATA | G | 4 | a0004c0112t0001g0119a0011c0027t0004g0150a0019c0093t0001g0159others(1): Show | 4 | HG01261.hp2 HG02056.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+880_3249+885d others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210225 | |||||
| chr12:109210225
|
GTGTATAT others(3): Show |
G | 1 | a0036c0094t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3249+874_3249+883d others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210225 | |||||
| chr12:109210227
|
G | A | 9 | a0001c0010t0001g0188a0001c0013t0001g0256a0002c0061t0003g0062others(6): Show | 9 | HG00280.hp2 HG00323.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3249+874G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210227 | ||||||
| chr12:109210227
|
GTA | G | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+878_3249+879d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210227 | |||||
| chr12:109210227
|
GTATATGT others(1): Show |
G | 10 | a0001c0003t0004g0074a0001c0012t0002g0045a0001c0012t0002g0259others(7): Show | 10 | HG01081.hp1 HG01884.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3249+888_3249+895d others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210227 | |||||
| chr12:109210229
|
A | G | 2 | a0003c0001t0001g0149a0009c0096t0009g0295 | 2 | HG02056.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3249+876A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210229 | ||||||
| chr12:109210231
|
A | ATATG | 13 | a0001c0011t0001g0013a0001c0039t0004g0039a0001c0039t0004g0116others(10): Show | 13 | HG02257.hp1 HG02615.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.3249+879_3249+880i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210231 | |||||
| chr12:109210231
|
A | ATG | 6 | a0001c0010t0001g0188a0001c0013t0001g0256a0002c0061t0003g0062others(3): Show | 6 | HG00280.hp2 HG00323.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.3249+880_3249+881d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210231 | |||||
| chr12:109210231
|
A | G | 3 | a0003c0001t0001g0149a0003c0081t0002g0230a0009c0096t0009g0295 | 3 | HG02056.hp2 HG02738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3249+878A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210231 | ||||||
| chr12:109210233
|
G | A | 62 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(59): Show | 62 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.3249+880G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210233 | ||||||
| chr12:109210235
|
A | ACATATAC others(63): Show |
1 | a0002c0007t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3249+882_3249+883i others(72): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210235 | ||||||
| chr12:109210235
|
A | ACATATAC others(11): Show |
1 | a0001c0098t0001g0286 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3249+882_3249+883i others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210235 | ||||||
| chr12:109210235
|
A | ACATATAC others(63): Show |
2 | a0001c0054t0001g0203a0007c0030t0004g0285 | 2 | HG01943.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3249+882_3249+883i others(72): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210235 | ||||||
| chr12:109210235
|
A | ACATATAC others(119): Show |
2 | a0001c0058t0016g0187a0002c0007t0022g0032 | 2 | HG01167.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3249+882_3249+883i others(128): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210235 | ||||||
| chr12:109210235
|
A | ACATATAC others(89): Show |
6 | a0001c0004t0017g0003a0001c0049t0001g0289a0001c0062t0019g0288others(3): Show | 6 | HG01884.hp2 HG02486.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3249+882_3249+883i others(98): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210235 | ||||||
| chr12:109210235
|
A | ACATATAC others(141): Show |
1 | a0001c0038t0001g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3249+882_3249+883i others(150): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210235 | ||||||
| chr12:109210235
|
A | ACATATAC others(155): Show |
1 | a0018c0051t0023g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3249+882_3249+883i others(164): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210235 | ||||||
| chr12:109210235
|
A | ACATATAC others(89): Show |
1 | a0014c0077t0004g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3249+882_3249+883i others(98): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210235 | ||||||
| chr12:109210235
|
A | ACATATAC others(115): Show |
2 | a0001c0004t0002g0054a0001c0011t0001g0056 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3249+882_3249+883i others(124): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210235 | ||||||
| chr12:109210235
|
A | ACATATAC others(63): Show |
1 | a0002c0007t0003g0041 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3249+882_3249+883i others(72): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210235 | ||||||
| chr12:109210235
|
A | ACATATAC others(89): Show |
1 | a0001c0048t0004g0307 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3249+882_3249+883i others(98): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210235 | ||||||
| chr12:109210235
|
A | ATATATAC others(11): Show |
1 | a0002c0024t0003g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3249+887_3249+888i others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(63): Show |
1 | a0001c0034t0001g0212 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3249+887_3249+888i others(72): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(89): Show |
1 | a0001c0034t0001g0211 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3249+887_3249+888i others(98): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(171): Show |
1 | a0002c0097t0003g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3249+887_3249+888i others(180): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(145): Show |
2 | a0001c0002t0001g0098a0001c0109t0002g0276 | 2 | HG01081.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.3249+887_3249+888i others(154): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(119): Show |
2 | a0001c0050t0001g0278a0041c0116t0003g0069 | 2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3249+887_3249+888i others(128): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(149): Show |
1 | a0001c0050t0001g0277 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3249+887_3249+888i others(158): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(93): Show |
2 | a0001c0023t0001g0100a0001c0023t0001g0122 | 2 | HG01515.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3249+887_3249+888i others(102): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(67): Show |
2 | a0002c0110t0003g0268a0003c0001t0001g0178 | 2 | HG01192.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.3249+887_3249+888i others(76): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(87): Show |
1 | a0001c0111t0001g0275 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3249+887_3249+888i others(96): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(15): Show |
1 | a0004c0040t0002g0213 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3249+887_3249+888i others(24): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(15): Show |
3 | a0001c0003t0002g0094a0001c0003t0002g0104a0001c0003t0002g0112 | 3 | HG03490.hp2 HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3249+887_3249+888i others(24): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(11): Show |
37 | a0001c0002t0001g0081a0001c0002t0001g0109a0001c0002t0001g0114others(34): Show | 37 | HG00408.hp2 HG00639.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.3249+887_3249+888i others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(41): Show |
1 | a0002c0043t0003g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3249+887_3249+888i others(50): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(37): Show |
1 | a0008c0015t0005g0168 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3249+887_3249+888i others(46): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(63): Show |
1 | a0002c0020t0003g0273 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3249+887_3249+888i others(72): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(35): Show |
1 | a0001c0108t0001g0010 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3249+887_3249+888i others(44): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATAC others(11): Show |
2 | a0009c0103t0004g0165a0034c0102t0018g0195 | 2 | HG01891.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3249+887_3249+888i others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | ATATATGC others(11): Show |
1 | a0001c0029t0002g0108 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3249+888_3249+889i others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210235 | |||||
| chr12:109210235
|
A | G | 61 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.3249+882A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210235 | ||||||
| chr12:109210237
|
ATATG | A | 35 | a0001c0002t0001g0126a0001c0002t0001g0241a0001c0002t0001g0242others(32): Show | 35 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.3249+888_3249+891d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210237 | |||||
| chr12:109210239
|
A | ATACACAC others(73): Show |
1 | a0033c0063t0010g0117 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3249+887_3249+888i others(82): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210239 | |||||
| chr12:109210239
|
A | ATACACGT others(21): Show |
1 | a0007c0037t0004g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3249+887_3249+888i others(30): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210239 | |||||
| chr12:109210239
|
A | ATATACAC others(73): Show |
1 | a0035c0076t0010g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3249+887_3249+888i others(82): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210239 | |||||
| chr12:109210239
|
A | G | 2 | a0003c0001t0001g0149a0009c0096t0009g0295 | 2 | HG02056.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3249+886A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210239 | ||||||
| chr12:109210240
|
TGTATATA others(3): Show |
T | 3 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3249+888_3249+897d others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210240 | ||||||
| chr12:109210240
|
TGTATATA others(29): Show |
T | 7 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3249+888_3249+923d others(38): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210240 | ||||||
| chr12:109210241
|
G | A | 60 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(57): Show | 60 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.3249+888G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210241 | ||||||
| chr12:109210244
|
T | C | 64 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(61): Show | 64 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.3249+891T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210244 | ||||||
| chr12:109210246
|
T | C | 90 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(87): Show | 90 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.3249+893T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210246 | ||||||
| chr12:109210247
|
A | G | 60 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(57): Show | 60 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.3249+894A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210247 | ||||||
| chr12:109210248
|
T | C | 38 | a0001c0002t0001g0126a0001c0002t0001g0241a0001c0002t0001g0242others(35): Show | 38 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.3249+895T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210248 | ||||||
| chr12:109210250
|
C | CATGT | 14 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0095t0001g0133others(11): Show | 14 | HG00323.hp1 HG02257.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.3249+898_3249+899i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210250 | |||||
| chr12:109210252
|
C | T | 94 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(91): Show | 94 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.3249+899C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210252 | ||||||
| chr12:109210253
|
A | ATG | 14 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0095t0001g0133others(11): Show | 14 | HG00323.hp1 HG02257.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.3249+900_3249+901i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210253 | ||||||
| chr12:109210253
|
A | G | 60 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(57): Show | 60 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.3249+900A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210253 | ||||||
| chr12:109210254
|
C | CGTGTGTA others(107): Show |
1 | a0031c0067t0003g0027 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3249+901_3249+902i others(116): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210254 | ||||||
| chr12:109210254
|
C | CGTGTGTA others(111): Show |
1 | a0005c0019t0003g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3249+901_3249+902i others(120): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210254 | ||||||
| chr12:109210254
|
C | CGTGTGTA others(115): Show |
1 | a0002c0036t0003g0161 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3249+901_3249+902i others(124): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210254 | ||||||
| chr12:109210254
|
C | CGTGTGTA others(113): Show |
1 | a0001c0004t0007g0028 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.3249+901_3249+902i others(122): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210254 | ||||||
| chr12:109210254
|
C | T | 111 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(108): Show | 111 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3249+901C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210254 | ||||||
| chr12:109210255
|
A | ACATATC | 5 | a0001c0003t0002g0094a0001c0003t0002g0112a0001c0050t0001g0277others(2): Show | 5 | HG01074.hp1 HG02523.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.3249+902_3249+903i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210255 | ||||||
| chr12:109210255
|
A | ACGTGTGT others(209): Show |
1 | a0001c0002t0001g0085 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3249+902_3249+903i others(218): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210255 | ||||||
| chr12:109210255
|
A | ATATC | 61 | a0001c0002t0001g0081a0001c0002t0001g0098a0001c0002t0001g0109others(58): Show | 61 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.3249+903_3249+904i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(127): Show |
1 | a0025c0090t0003g0130 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3249+914_3249+915i others(136): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(171): Show |
1 | a0002c0028t0003g0228 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3249+916_3249+917i others(180): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(161): Show |
1 | a0002c0021t0006g0239 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3249+916_3249+917i others(170): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(161): Show |
1 | a0002c0007t0003g0026 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3249+916_3249+917i others(170): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(107): Show |
1 | a0010c0042t0003g0220 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3249+916_3249+917i others(116): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(139): Show |
1 | a0004c0041t0002g0222 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.3249+916_3249+917i others(148): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(115): Show |
3 | a0001c0002t0008g0306a0004c0008t0008g0263a0010c0073t0014g0208 | 3 | NA18974.hp2 NA18992.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.3249+916_3249+917i others(124): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(83): Show |
1 | a0001c0004t0002g0050 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3249+916_3249+917i others(92): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(145): Show |
1 | a0001c0046t0002g0190 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3249+916_3249+917i others(154): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(143): Show |
1 | a0001c0046t0002g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3249+916_3249+917i others(152): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(187): Show |
1 | a0001c0087t0001g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3249+916_3249+917i others(196): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(109): Show |
1 | a0024c0091t0002g0174 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3249+916_3249+917i others(118): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(135): Show |
1 | a0002c0021t0003g0252 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3249+916_3249+917i others(144): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(197): Show |
2 | a0001c0089t0002g0162a0005c0019t0003g0271 | 2 | NA18955.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3249+916_3249+917i others(206): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(187): Show |
1 | a0002c0021t0006g0255 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3249+916_3249+917i others(196): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(161): Show |
3 | a0002c0007t0006g0017a0002c0036t0006g0223a0022c0084t0004g0254 | 3 | HG00558.hp1 HG02080.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.3249+916_3249+917i others(170): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(135): Show |
7 | a0001c0048t0002g0281a0001c0049t0004g0088a0002c0014t0003g0083others(4): Show | 7 | HG00735.hp1 HG01109.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.3249+916_3249+917i others(144): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(159): Show |
1 | a0005c0019t0006g0076 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3249+916_3249+917i others(168): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(109): Show |
10 | a0001c0038t0001g0029a0001c0045t0002g0234a0002c0020t0003g0232others(7): Show | 10 | HG02698.hp2 HG03492.hp1 HG03654.hp1 others(7): Show |
intron_variant | MODIFIER | c.3249+916_3249+917i others(118): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(161): Show |
1 | a0002c0007t0003g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3249+916_3249+917i others(170): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(107): Show |
1 | a0002c0014t0003g0106 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3249+916_3249+917i others(116): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(83): Show |
7 | a0001c0004t0007g0001a0001c0004t0007g0011a0001c0004t0007g0019others(4): Show | 8 | HG02083.hp1 HG04204.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.3249+916_3249+917i others(92): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(187): Show |
1 | a0001c0045t0002g0146 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3249+916_3249+917i others(196): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | ATGTGTGT others(111): Show |
1 | a0002c0014t0003g0015 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3249+916_3249+917i others(120): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210255 | |||||
| chr12:109210255
|
A | C | 39 | a0001c0002t0001g0126a0001c0002t0001g0241a0001c0002t0001g0242others(36): Show | 39 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.3249+902A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210255 | ||||||
| chr12:109210255
|
A | G | 9 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0012t0002g0259others(6): Show | 9 | HG00280.hp2 HG01261.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.3249+902A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210255 | ||||||
| chr12:109210256
|
T | C | 3 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3249+903T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210256 | ||||||
| chr12:109210257
|
G | C | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3249+904G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210257 | ||||||
| chr12:109210258
|
T | C | 1 | a0003c0001t0001g0178 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3249+905T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210258 | ||||||
| chr12:109210261
|
G | A | 2 | a0002c0070t0005g0199a0021c0068t0001g0202 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3249+908G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210261 | ||||||
| chr12:109210261
|
G | GTA | 5 | a0001c0013t0001g0256a0004c0112t0001g0119a0011c0027t0004g0150others(2): Show | 5 | HG00280.hp2 HG01261.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.3249+912_3249+913d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210261 | |||||
| chr12:109210265
|
A | ATATG | 74 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(71): Show | 74 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.3249+913_3249+914i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210265 | |||||
| chr12:109210267
|
G | A | 6 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0001g0188others(3): Show | 6 | HG02056.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3249+914G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210267 | ||||||
| chr12:109210268
|
TAC | T | 15 | a0001c0003t0004g0300a0001c0010t0002g0016a0001c0064t0009g0184others(12): Show | 15 | HG00558.hp2 HG00642.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.3249+917_3249+918d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210268 | |||||
| chr12:109210269
|
A | ATATATG | 11 | a0001c0016t0011g0274a0007c0037t0004g0200a0007c0057t0004g0207others(8): Show | 11 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.3249+916_3249+917i others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210269 | ||||||
| chr12:109210269
|
A | ATATATGT others(77): Show |
1 | a0002c0017t0003g0024 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3249+916_3249+917i others(86): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210269 | ||||||
| chr12:109210269
|
A | ATATATGT others(103): Show |
1 | a0001c0004t0002g0052 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3249+916_3249+917i others(112): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210269 | ||||||
| chr12:109210269
|
A | G | 6 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0001g0188others(3): Show | 6 | HG02056.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3249+916A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210269 | ||||||
| chr12:109210270
|
C | CATATACA others(49): Show |
1 | a0002c0028t0003g0160 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3249+928_3249+929i others(58): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210270 | |||||
| chr12:109210270
|
C | CATATACA others(127): Show |
1 | a0002c0028t0003g0179 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3249+928_3249+929i others(136): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210270 | |||||
| chr12:109210270
|
C | T | 268 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.3249+917C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210270 | ||||||
| chr12:109210276
|
C | T | 28 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0004t0002g0052others(25): Show | 28 | HG00597.hp1 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.3249+923C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210276 | ||||||
| chr12:109210278
|
C | T | 21 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(18): Show | 21 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.3249+925C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210278 | ||||||
| chr12:109210279
|
A | G | 24 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(21): Show | 24 | HG00323.hp1 HG01261.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.3249+926A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210279 | ||||||
| chr12:109210280
|
C | CATGTGTG others(13): Show |
1 | a0001c0012t0002g0251 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3249+928_3249+929i others(22): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210280 | |||||
| chr12:109210280
|
C | T | 25 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(22): Show | 25 | HG00323.hp1 HG01261.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.3249+927C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210280 | ||||||
| chr12:109210281
|
ACATATC | A | 12 | a0001c0003t0004g0074a0001c0012t0002g0045a0001c0012t0002g0250others(9): Show | 12 | HG00673.hp1 HG01081.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3249+929_3249+934d others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210281 | ||||||
| chr12:109210282
|
C | T | 56 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(53): Show | 56 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.3249+929C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210282 | ||||||
| chr12:109210282
|
CAT | C | 3 | a0001c0010t0001g0188a0001c0011t0001g0013a0002c0061t0003g0062 | 3 | HG02723.hp2 HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3249+932_3249+933d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210282 | |||||
| chr12:109210283
|
A | G | 57 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.3249+930A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210283 | ||||||
| chr12:109210284
|
T | C | 2 | a0001c0012t0002g0251a0002c0017t0003g0025 | 2 | HG03831.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3249+931T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210284 | ||||||
| chr12:109210285
|
A | G | 87 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(84): Show | 87 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.3249+932A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210285 | ||||||
| chr12:109210286
|
T | C | 2 | a0001c0012t0002g0251a0002c0017t0003g0025 | 2 | HG03831.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3249+933T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210286 | ||||||
| chr12:109210287
|
C | A | 79 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0191others(76): Show | 79 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.3249+934C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210287 | ||||||
| chr12:109210287
|
C | G | 12 | a0001c0002t0001g0079a0001c0002t0001g0091a0001c0010t0001g0188others(9): Show | 12 | HG00280.hp2 HG00741.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.3249+934C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210287 | ||||||
| chr12:109210287
|
CTG | C | 15 | a0001c0004t0007g0001a0001c0004t0007g0011a0001c0004t0007g0019others(12): Show | 16 | HG01884.hp1 HG01891.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.3249+940_3249+941d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210287 | |||||
| chr12:109210289
|
G | A | 56 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.3249+936G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210289 | ||||||
| chr12:109210289
|
G | C | 1 | a0027c0065t0005g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3249+936G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210289 | ||||||
| chr12:109210289
|
G | GTA | 4 | a0007c0037t0004g0200a0009c0096t0009g0295a0033c0063t0010g0117others(1): Show | 4 | HG02145.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+937_3249+938i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210289 | |||||
| chr12:109210290
|
T | C | 3 | a0002c0110t0003g0268a0003c0001t0001g0178a0041c0116t0003g0069 | 3 | HG01192.hp2 HG01943.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.3249+937T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210290 | ||||||
| chr12:109210291
|
G | A | 7 | a0001c0002t0001g0079a0001c0002t0001g0091a0003c0001t0001g0149others(4): Show | 7 | HG00741.hp1 HG01070.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.3249+938G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210291 | ||||||
| chr12:109210291
|
GTGTA | G | 3 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3249+940_3249+943d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210291 | |||||
| chr12:109210293
|
G | A | 90 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0085others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.3249+940G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210293 | ||||||
| chr12:109210296
|
T | C | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3249+943T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210296 | ||||||
| chr12:109210297
|
A | ATATG | 24 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(21): Show | 24 | HG00323.hp1 HG01261.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.3249+945_3249+946i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210297 | |||||
| chr12:109210299
|
G | A | 21 | a0001c0002t0001g0079a0001c0002t0001g0091a0001c0011t0001g0157others(18): Show | 21 | HG00741.hp1 HG01070.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.3249+946G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210299 | ||||||
| chr12:109210301
|
A | G | 8 | a0001c0002t0001g0079a0001c0002t0001g0091a0001c0016t0011g0274others(5): Show | 8 | HG00741.hp1 HG01070.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.3249+948A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210301 | ||||||
| chr12:109210302
|
T | C | 4 | a0002c0017t0003g0025a0003c0001t0001g0145a0006c0078t0001g0181others(1): Show | 4 | HG03831.hp1 NA18992.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+949T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210302 | ||||||
| chr12:109210306
|
T | C | 17 | a0001c0004t0017g0003a0001c0016t0011g0274a0001c0038t0001g0201others(14): Show | 17 | HG01069.hp1 HG01074.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.3249+953T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210306 | ||||||
| chr12:109210306
|
TAC | T | 3 | a0001c0004t0002g0054a0007c0057t0004g0207a0039c0080t0010g0071 | 3 | HG03195.hp1 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3249+961_3249+962d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210306 | |||||
| chr12:109210307
|
A | ACACACAC others(27): Show |
2 | a0001c0054t0001g0203a0010c0042t0003g0220 | 2 | HG01167.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.3249+971_3249+972i others(36): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210307 | |||||
| chr12:109210307
|
A | ACG | 11 | a0001c0004t0017g0003a0001c0038t0001g0201a0001c0048t0004g0307others(8): Show | 11 | HG01074.hp1 HG01169.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.3249+955_3249+956i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210307 | |||||
| chr12:109210308
|
C | CACACACA others(23): Show |
1 | a0002c0017t0003g0024 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3249+971_3249+972i others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210308 | |||||
| chr12:109210308
|
C | T | 8 | a0001c0002t0001g0079a0001c0002t0001g0091a0001c0016t0011g0274others(5): Show | 8 | HG00741.hp1 HG01070.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.3249+955C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210308 | ||||||
| chr12:109210309
|
A | G | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3249+956A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210309 | ||||||
| chr12:109210310
|
C | CGT | 4 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(1): Show | 4 | HG00280.hp2 HG02723.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.3249+957_3249+958i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210310 | ||||||
| chr12:109210310
|
C | T | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+957C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210310 | ||||||
| chr12:109210311
|
A | G | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+958A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210311 | ||||||
| chr12:109210312
|
C | CATGTGTG others(13): Show |
1 | a0006c0120t0003g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3249+960_3249+961i others(22): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210312 | |||||
| chr12:109210312
|
C | T | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+959C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210312 | ||||||
| chr12:109210313
|
A | ATG | 52 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0191others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.3249+960_3249+961i others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210313 | ||||||
| chr12:109210313
|
ACATATC | A | 3 | a0003c0001t0001g0145a0006c0078t0001g0181a0008c0044t0003g0182 | 3 | NA18992.hp2 NA19060.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3249+961_3249+966d others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210313 | ||||||
| chr12:109210314
|
C | T | 61 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0191others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.3249+961C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210314 | ||||||
| chr12:109210315
|
A | ATGTG | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+963_3249+964i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210315 | |||||
| chr12:109210315
|
A | G | 61 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0191others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.3249+962A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210315 | ||||||
| chr12:109210316
|
T | C | 2 | a0006c0120t0003g0043a0021c0068t0001g0202 | 2 | HG01109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3249+963T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210316 | ||||||
| chr12:109210317
|
A | G | 59 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(56): Show | 59 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.3249+964A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210317 | ||||||
| chr12:109210318
|
T | C | 1 | a0006c0120t0003g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3249+965T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210318 | ||||||
| chr12:109210319
|
C | A | 78 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0191others(75): Show | 78 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.3249+966C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210319 | ||||||
| chr12:109210319
|
C | G | 6 | a0001c0002t0001g0079a0001c0002t0001g0091a0001c0010t0001g0188others(3): Show | 6 | HG00280.hp2 HG00741.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.3249+966C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210319 | ||||||
| chr12:109210321
|
G | A | 77 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0191others(74): Show | 77 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.3249+968G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210321 | ||||||
| chr12:109210325
|
A | ATATGTAT others(23): Show |
1 | a0001c0004t0002g0052 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3249+975_3249+976i others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210325 | |||||
| chr12:109210325
|
A | G | 81 | a0001c0002t0001g0114a0001c0002t0021g0243a0001c0003t0002g0102others(78): Show | 82 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.3249+972A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210325 | ||||||
| chr12:109210328
|
T | C | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3249+975T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210328 | ||||||
| chr12:109210331
|
G | GTGTA | 4 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(1): Show | 4 | HG00280.hp2 HG02723.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.3249+979_3249+980i others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210331 | |||||
| chr12:109210337
|
ACACG | A | 57 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.3249+988_3249+991d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210337 | |||||
| chr12:109210338
|
C | T | 42 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(39): Show | 42 | HG00323.hp1 HG00642.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.3249+985C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210338 | ||||||
| chr12:109210339
|
ACG | A | 18 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(15): Show | 18 | HG00642.hp1 HG00673.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.3249+988_3249+989d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210339 | |||||
| chr12:109210341
|
G | A | 28 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(25): Show | 28 | HG00280.hp2 HG00323.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.3249+988G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210341 | ||||||
| chr12:109210342
|
C | CACATGTG others(23): Show |
3 | a0004c0112t0001g0119a0011c0027t0004g0150a0029c0085t0003g0238 | 3 | HG01261.hp2 HG02056.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.3249+992_3249+993i others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210342 | |||||
| chr12:109210342
|
C | CATGTGTA others(53): Show |
3 | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256 | 3 | HG00280.hp2 HG02723.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3249+990_3249+991i others(62): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210342 | |||||
| chr12:109210342
|
C | CATGTGTA others(53): Show |
1 | a0002c0061t0003g0062 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3249+990_3249+991i others(62): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210342 | |||||
| chr12:109210342
|
C | T | 57 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.3249+989C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210342 | ||||||
| chr12:109210344
|
C | CATGTGTG others(21): Show |
1 | a0019c0093t0001g0159 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3249+992_3249+993i others(30): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210344 | |||||
| chr12:109210346
|
C | T | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+993C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210346 | ||||||
| chr12:109210347
|
A | G | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+994A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210347 | ||||||
| chr12:109210348
|
C | T | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+995C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210348 | ||||||
| chr12:109210349
|
A | G | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+996A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210349 | ||||||
| chr12:109210349
|
ATATC | A | 6 | a0003c0001t0001g0149a0009c0025t0001g0105a0009c0025t0001g0269others(3): Show | 6 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.3249+998_3249+1001 others(7): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210349 | |||||
| chr12:109210351
|
A | G | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+998A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210351 | ||||||
| chr12:109210353
|
C | A | 21 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(18): Show | 21 | HG00323.hp1 HG01891.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.3249+1000C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210353 | ||||||
| chr12:109210353
|
C | CTGTGTAT others(23): Show |
3 | a0001c0046t0002g0067a0001c0046t0002g0190a0002c0024t0003g0093 | 3 | HG02523.hp2 NA18959.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.3249+1057_3249+108 others(34): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210353 | |||||
| chr12:109210355
|
G | A | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+1002G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210355 | ||||||
| chr12:109210355
|
G | GTGTATAT others(1): Show |
63 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(60): Show | 63 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.3249+1011_3249+101 others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210355 | |||||
| chr12:109210359
|
A | G | 29 | a0001c0004t0002g0052a0001c0004t0007g0001a0001c0004t0007g0011others(26): Show | 30 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.3249+1006A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210359 | ||||||
| chr12:109210362
|
T | C | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3249+1009T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210362 | ||||||
| chr12:109210372
|
C | T | 2 | a0033c0063t0010g0117a0035c0076t0010g0267 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3249+1019C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210372 | ||||||
| chr12:109210375
|
G | A | 22 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(19): Show | 22 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.3249+1022G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210375 | ||||||
| chr12:109210380
|
C | CACATGTG others(23): Show |
3 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3249+1056_3249+105 others(34): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210380 | |||||
| chr12:109210380
|
C | T | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+1027C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210380 | ||||||
| chr12:109210382
|
C | T | 22 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(19): Show | 22 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.3249+1029C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210382 | ||||||
| chr12:109210383
|
A | ATATC | 3 | a0002c0006t0003g0092a0002c0017t0003g0025a0006c0120t0003g0043 | 3 | HG00642.hp1 HG01109.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.3249+1031_3249+103 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210383 | |||||
| chr12:109210383
|
A | ATC | 5 | a0003c0001t0001g0145a0006c0078t0001g0181a0008c0044t0003g0182others(2): Show | 5 | HG03098.hp2 HG03225.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.3249+1031_3249+103 others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210383 | |||||
| chr12:109210383
|
A | C | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+1030A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210383 | ||||||
| chr12:109210389
|
A | G | 3 | a0003c0001t0001g0145a0006c0078t0001g0181a0008c0044t0003g0182 | 3 | NA18992.hp2 NA19060.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3249+1036A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210389 | ||||||
| chr12:109210392
|
T | C | 2 | a0021c0068t0001g0202a0039c0080t0010g0071 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3249+1039T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210392 | ||||||
| chr12:109210410
|
C | T | 21 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0009g0186others(18): Show | 21 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.3249+1057C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210410 | ||||||
| chr12:109210422
|
T | C | 8 | a0001c0016t0011g0274a0007c0037t0004g0200a0007c0057t0004g0207others(5): Show | 8 | HG02145.hp2 HG02965.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3249+1069T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210422 | ||||||
| chr12:109210440
|
T | C | 34 | a0001c0003t0002g0104a0001c0034t0001g0211a0001c0034t0001g0212others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.3249+1087T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210440 | ||||||
| chr12:109210447
|
GTA | G | 64 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(61): Show | 64 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.3249+1100_3249+110 others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210447 | |||||
| chr12:109210451
|
A | G | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+1098A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210451 | ||||||
| chr12:109210452
|
T | C | 2 | a0033c0063t0010g0117a0035c0076t0010g0267 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3249+1099T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210452 | ||||||
| chr12:109210453
|
A | G | 3 | a0002c0028t0003g0179a0025c0090t0003g0130a0036c0094t0004g0072 | 3 | HG02132.hp1 HG02922.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.3249+1100A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210453 | ||||||
| chr12:109210458
|
T | C | 5 | a0007c0037t0004g0200a0007c0057t0004g0207a0033c0063t0010g0117others(2): Show | 5 | HG02145.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3249+1105T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210458 | ||||||
| chr12:109210462
|
T | C | 17 | a0001c0002t0001g0098a0001c0003t0002g0104a0001c0048t0002g0281others(14): Show | 17 | HG00642.hp1 HG01081.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.3249+1109T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210462 | ||||||
| chr12:109210463
|
A | G | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+1110A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210463 | ||||||
| chr12:109210483
|
G | A | 1 | a0003c0005t0002g0264 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3249+1130G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210483 | ||||||
| chr12:109210484
|
T | C | 1 | a0001c0003t0004g0300 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3249+1131T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210484 | ||||||
| chr12:109210492
|
T | C | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+1139T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210492 | ||||||
| chr12:109210495
|
A | G | 1 | a0005c0009t0006g0177 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3249+1142A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210495 | ||||||
| chr12:109210497
|
G | A | 2 | a0001c0002t0001g0241a0001c0002t0001g0242 | 2 | NA18955.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.3249+1144G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210497 | ||||||
| chr12:109210516
|
T | C | 1 | a0001c0074t0004g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3249+1163T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210516 | ||||||
| chr12:109210532
|
T | A | 2 | a0013c0033t0002g0185a0013c0033t0002g0189 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3249+1179T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210532 | ||||||
| chr12:109210539
|
A | G | 2 | a0006c0026t0002g0155a0006c0026t0002g0156 | 2 | HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3249+1186A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210539 | ||||||
| chr12:109210541
|
G | A | 115 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(112): Show | 115 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.3249+1188G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210541 | ||||||
| chr12:109210554
|
T | C | 64 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(61): Show | 64 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.3249+1201T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210554 | ||||||
| chr12:109210564
|
C | T | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+1211C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210564 | ||||||
| chr12:109210601
|
A | G | 11 | a0001c0002t0008g0306a0001c0045t0002g0234a0002c0020t0003g0232others(8): Show | 11 | NA18612.hp1 NA18952.hp1 NA18970.hp1 others(8): Show |
intron_variant | MODIFIER | c.3249+1248A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210601 | ||||||
| chr12:109210653
|
G | A | 64 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(61): Show | 64 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.3249+1300G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210653 | ||||||
| chr12:109210752
|
TA | T | 13 | a0001c0016t0011g0274a0005c0009t0006g0257a0007c0037t0004g0200others(10): Show | 13 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.3249+1411delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210752 | |||||
| chr12:109210800
|
A | G | 3 | a0001c0069t0002g0204a0001c0124t0012g0197a0002c0092t0010g0192 | 3 | HG03579.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3249+1447A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210800 | ||||||
| chr12:109210847
|
G | A | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+1494G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109210847 | ||||||
| chr12:109210948
|
T | TA | 6 | a0001c0003t0004g0074a0001c0013t0001g0256a0006c0113t0004g0031others(3): Show | 6 | HG00280.hp2 HG01081.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.3249+1608dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109210948 | |||||
| chr12:109211014
|
G | T | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3249+1661G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109211014 | ||||||
| chr12:109211020
|
CGTT | C | 5 | a0007c0037t0004g0200a0007c0057t0004g0207a0033c0063t0010g0117others(2): Show | 5 | HG02145.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3249+1671_3249+167 others(7): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109211020 | |||||
| chr12:109211207
|
G | A | 64 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(61): Show | 64 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.3250-1629G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109211207 | ||||||
| chr12:109211223
|
G | A | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3250-1613G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109211223 | ||||||
| chr12:109211335
|
GATTCCTC others(20): Show |
G | 1 | a0002c0020t0003g0273 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3250-1500_3250-147 others(31): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109211335 | ||||||
| chr12:109211342
|
C | CT | 14 | a0001c0003t0002g0244a0001c0004t0002g0052a0001c0022t0004g0007others(11): Show | 14 | HG00597.hp1 HG02027.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.3250-1472dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109211342 | |||||
| chr12:109211342
|
CT | C | 86 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(83): Show | 86 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.3250-1472delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109211342 | |||||
| chr12:109211342
|
CTT | C | 8 | a0001c0002t0001g0191a0001c0011t0001g0008a0001c0016t0011g0274others(5): Show | 8 | HG00323.hp2 HG00597.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.3250-1473_3250-147 others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109211342 | |||||
| chr12:109211437
|
A | G | 115 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(112): Show | 115 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.3250-1399A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109211437 | ||||||
| chr12:109211505
|
G | A | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3250-1331G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109211505 | ||||||
| chr12:109211512
|
C | T | 1 | a0011c0027t0013g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3250-1324C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109211512 | ||||||
| chr12:109211557
|
G | C | 1 | a0002c0017t0003g0042 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3250-1279G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109211557 | ||||||
| chr12:109211605
|
G | A | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3250-1231G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109211605 | ||||||
| chr12:109211669
|
T | C | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3250-1167T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109211669 | ||||||
| chr12:109211692
|
C | T | 57 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.3250-1144C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109211692 | ||||||
| chr12:109211901
|
GT | G | 11 | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(8): Show | 11 | HG00673.hp1 HG02040.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.3250-926delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | 109211901 | |||||
| chr12:109211945
|
C | T | 1 | a0001c0012t0002g0262 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3250-891C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109211945 | ||||||
| chr12:109212045
|
T | C | 1 | a0003c0001t0001g0141 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3250-791T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109212045 | ||||||
| chr12:109212245
|
G | T | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3250-591G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109212245 | ||||||
| chr12:109212360
|
C | T | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3250-476C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109212360 | ||||||
| chr12:109212549
|
C | T | 1 | a0001c0003t0004g0074 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3250-287C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109212549 | ||||||
| chr12:109212557
|
C | T | 1 | a0003c0001t0001g0138 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3250-279C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109212557 | ||||||
| chr12:109212599
|
C | T | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3250-237C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109212599 | ||||||
| chr12:109212667
|
A | G | 1 | a0006c0120t0003g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3250-169A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109212667 | ||||||
| chr12:109212668
|
T | C | 1 | a0001c0048t0004g0307 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3250-168T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109212668 | ||||||
| chr12:109212741
|
T | C | 74 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(71): Show | 74 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.3250-95T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | 109212741 | ||||||
| chr12:109213025
|
G | A | 2 | a0003c0001t0001g0158a0003c0001t0001g0265 | 2 | HG02040.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.3350+89G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109213025 | ||||||
| chr12:109213070
|
A | G | 9 | a0001c0003t0004g0074a0001c0064t0009g0184a0002c0017t0003g0042others(6): Show | 9 | HG01081.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.3350+134A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109213070 | ||||||
| chr12:109213117
|
T | G | 1 | a0006c0026t0002g0156 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3350+181T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109213117 | ||||||
| chr12:109213189
|
G | T | 1 | a0001c0023t0001g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3350+253G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109213189 | ||||||
| chr12:109213366
|
T | C | 6 | a0001c0003t0004g0074a0002c0017t0003g0042a0006c0113t0004g0031others(3): Show | 6 | HG01081.hp1 HG01884.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3350+430T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109213366 | ||||||
| chr12:109213419
|
C | T | 14 | a0001c0002t0001g0085a0001c0002t0001g0098a0001c0023t0001g0100others(11): Show | 14 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.3350+483C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109213419 | ||||||
| chr12:109213494
|
G | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3350+558G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109213494 | ||||||
| chr12:109213732
|
G | C | 3 | a0002c0021t0003g0253a0002c0024t0003g0034a0002c0024t0003g0036 | 3 | NA18612.hp1 NA19009.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.3350+796G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109213732 | ||||||
| chr12:109213923
|
T | C | 1 | a0001c0010t0002g0261 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3350+987T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109213923 | ||||||
| chr12:109214091
|
C | CA | 73 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(70): Show | 73 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.3350+1165dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | INFO_REALIGN_3_PRIME | chr12 | 109214091 | |||||
| chr12:109214102
|
G | GA | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3350+1176dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | INFO_REALIGN_3_PRIME | chr12 | 109214102 | |||||
| chr12:109214219
|
G | A | 1 | a0001c0046t0002g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3350+1283G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109214219 | ||||||
| chr12:109214348
|
G | A | 1 | a0005c0019t0003g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3350+1412G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109214348 | ||||||
| chr12:109214510
|
C | T | 64 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(61): Show | 64 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.3350+1574C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109214510 | ||||||
| chr12:109214544
|
A | G | 5 | a0001c0002t0001g0081a0002c0006t0003g0092a0002c0006t0003g0095others(2): Show | 5 | HG00639.hp2 HG00642.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.3350+1608A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109214544 | ||||||
| chr12:109214576
|
A | G | 1 | a0001c0011t0001g0008 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3350+1640A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109214576 | ||||||
| chr12:109214595
|
C | A | 115 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(112): Show | 115 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.3350+1659C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109214595 | ||||||
| chr12:109214617
|
C | T | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3350+1681C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109214617 | ||||||
| chr12:109214726
|
C | CA | 5 | a0007c0037t0004g0200a0007c0057t0004g0207a0033c0063t0010g0117others(2): Show | 5 | HG02145.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3350+1792dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | INFO_REALIGN_3_PRIME | chr12 | 109214726 | |||||
| chr12:109214835
|
C | T | 1 | a0003c0001t0001g0064 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3351-1783C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109214835 | ||||||
| chr12:109214871
|
A | G | 106 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(103): Show | 106 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.3351-1747A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109214871 | ||||||
| chr12:109215104
|
GA | G | 10 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0009g0186others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.3351-1503delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | INFO_REALIGN_3_PRIME | chr12 | 109215104 | |||||
| chr12:109215266
|
G | A | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3351-1352G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109215266 | ||||||
| chr12:109215335
|
G | A | 2 | a0001c0074t0004g0229a0002c0070t0005g0199 | 2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3351-1283G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109215335 | ||||||
| chr12:109215442
|
A | C | 2 | a0001c0010t0009g0186a0001c0016t0009g0290 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3351-1176A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109215442 | ||||||
| chr12:109215477
|
T | A | 13 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0009g0186others(10): Show | 13 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3351-1141T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109215477 | ||||||
| chr12:109215538
|
C | T | 1 | a0001c0018t0011g0047 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3351-1080C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109215538 | ||||||
| chr12:109215644
|
A | G | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3351-974A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109215644 | ||||||
| chr12:109215652
|
C | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3351-966C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109215652 | ||||||
| chr12:109215682
|
G | A | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3351-936G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109215682 | ||||||
| chr12:109215697
|
G | A | 24 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0009g0186others(21): Show | 24 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.3351-921G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109215697 | ||||||
| chr12:109215765
|
C | CA | 10 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0009g0186others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.3351-842dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | INFO_REALIGN_3_PRIME | chr12 | 109215765 | |||||
| chr12:109215987
|
C | G | 1 | a0002c0024t0003g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3351-631C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109215987 | ||||||
| chr12:109216011
|
C | T | 86 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(83): Show | 86 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.3351-607C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109216011 | ||||||
| chr12:109216219
|
C | CT | 8 | a0001c0010t0001g0188a0001c0016t0011g0274a0001c0087t0001g0236others(5): Show | 8 | HG00438.hp2 HG01069.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.3351-379dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | INFO_REALIGN_3_PRIME | chr12 | 109216219 | |||||
| chr12:109216219
|
C | CTT | 10 | a0002c0061t0003g0062a0002c0086t0003g0260a0011c0027t0004g0150others(7): Show | 10 | HG01168.hp2 HG01261.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.3351-380_3351-379d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | INFO_REALIGN_3_PRIME | chr12 | 109216219 | |||||
| chr12:109216219
|
CT | C | 7 | a0001c0003t0004g0074a0001c0018t0002g0048a0001c0046t0002g0190others(4): Show | 7 | HG00323.hp1 HG01070.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.3351-379delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | INFO_REALIGN_3_PRIME | chr12 | 109216219 | |||||
| chr12:109216221
|
T | C | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3351-397T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109216221 | ||||||
| chr12:109216222
|
T | C | 1 | a0006c0026t0016g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3351-396T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109216222 | ||||||
| chr12:109216352
|
G | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3351-266G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109216352 | ||||||
| chr12:109216408
|
G | A | 85 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(82): Show | 85 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.3351-210G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109216408 | ||||||
| chr12:109216481
|
A | G | 11 | a0001c0003t0004g0300a0002c0006t0005g0284a0002c0006t0005g0294others(8): Show | 11 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.3351-137A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | chr12 | 109216481 | ||||||
| chr12:109216566
|
AG | A | 3 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3351-50delG | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | INFO_REALIGN_3_PRIME | chr12 | 109216566 | |||||
| chr12:109217078
|
T | G | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3564+158T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109217078 | ||||||
| chr12:109217301
|
A | C | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3564+381A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109217301 | ||||||
| chr12:109217349
|
T | G | 61 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(58): Show | 61 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.3564+429T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109217349 | ||||||
| chr12:109217446
|
C | T | 4 | a0001c0124t0012g0197a0002c0092t0010g0192a0007c0037t0004g0200others(1): Show | 4 | HG02145.hp2 HG03540.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3564+526C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109217446 | ||||||
| chr12:109217601
|
C | T | 2 | a0001c0016t0011g0274a0021c0068t0001g0202 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3564+681C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109217601 | ||||||
| chr12:109217616
|
T | C | 3 | a0033c0063t0010g0117a0035c0076t0010g0267a0039c0080t0010g0071 | 3 | HG03098.hp2 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3564+696T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109217616 | ||||||
| chr12:109217710
|
GGATT | G | 27 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(24): Show | 27 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.3564+792_3564+795d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109217710 | |||||
| chr12:109217715
|
G | C | 27 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(24): Show | 27 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.3564+795G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109217715 | ||||||
| chr12:109217936
|
A | C | 1 | a0001c0010t0002g0021 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3564+1016A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109217936 | ||||||
| chr12:109218103
|
G | A | 26 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(23): Show | 26 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.3564+1183G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109218103 | ||||||
| chr12:109218236
|
C | G | 3 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3564+1316C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109218236 | ||||||
| chr12:109218262
|
T | C | 119 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(116): Show | 119 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.3564+1342T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109218262 | ||||||
| chr12:109218263
|
G | A | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3564+1343G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109218263 | ||||||
| chr12:109218331
|
A | G | 13 | a0001c0003t0004g0074a0002c0017t0003g0042a0002c0043t0003g0012others(10): Show | 13 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.3564+1411A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109218331 | ||||||
| chr12:109218367
|
A | AGTTT | 22 | a0001c0002t0001g0126a0001c0002t0008g0306a0001c0003t0002g0097others(19): Show | 22 | HG00438.hp1 HG00558.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.3564+1480_3564+148 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109218367 | |||||
| chr12:109218367
|
AGTTT | A | 14 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0074t0004g0229others(11): Show | 14 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.3564+1480_3564+148 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109218367 | |||||
| chr12:109218367
|
AGTTTGTT others(1): Show |
A | 61 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(58): Show | 61 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.3564+1476_3564+148 others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109218367 | |||||
| chr12:109218636
|
A | G | 1 | a0004c0008t0008g0219 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3564+1716A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109218636 | ||||||
| chr12:109218652
|
A | AT | 10 | a0001c0003t0002g0244a0001c0010t0002g0016a0001c0011t0001g0013others(7): Show | 10 | HG00621.hp1 HG00621.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.3564+1751dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109218652 | |||||
| chr12:109218652
|
AT | A | 8 | a0001c0002t0008g0306a0001c0003t0002g0104a0001c0003t0002g0193others(5): Show | 8 | HG01175.hp2 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.3564+1751delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109218652 | |||||
| chr12:109218693
|
G | A | 10 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0009g0186others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.3564+1773G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109218693 | ||||||
| chr12:109218716
|
T | C | 116 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(113): Show | 116 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.3564+1796T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109218716 | ||||||
| chr12:109218723
|
G | C | 1 | a0011c0027t0004g0150 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3564+1803G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109218723 | ||||||
| chr12:109218739
|
C | T | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3564+1819C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109218739 | ||||||
| chr12:109218740
|
G | A | 24 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(21): Show | 24 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.3564+1820G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109218740 | ||||||
| chr12:109218771
|
C | CT | 66 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.3564+1866dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109218771 | |||||
| chr12:109218771
|
CT | C | 6 | a0001c0046t0002g0190a0005c0009t0003g0164a0005c0009t0006g0148others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.3564+1866delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109218771 | |||||
| chr12:109218828
|
G | T | 1 | a0006c0120t0003g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3564+1908G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109218828 | ||||||
| chr12:109218859
|
C | T | 27 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(24): Show | 27 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.3564+1939C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109218859 | ||||||
| chr12:109219005
|
G | A | 61 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(58): Show | 61 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.3564+2085G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109219005 | ||||||
| chr12:109219019
|
G | A | 3 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3564+2099G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109219019 | ||||||
| chr12:109219062
|
C | T | 4 | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0055t0001g0226others(1): Show | 4 | HG01433.hp1 HG02630.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3564+2142C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109219062 | ||||||
| chr12:109219393
|
T | G | 1 | a0018c0051t0023g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3564+2473T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109219393 | ||||||
| chr12:109219416
|
A | T | 2 | a0001c0016t0011g0274a0021c0068t0001g0202 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3564+2496A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109219416 | ||||||
| chr12:109219436
|
C | G | 1 | a0002c0088t0006g0247 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3564+2516C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109219436 | ||||||
| chr12:109219669
|
G | A | 1 | a0003c0001t0001g0138 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3564+2749G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109219669 | ||||||
| chr12:109219678
|
T | C | 7 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3564+2758T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109219678 | ||||||
| chr12:109219759
|
A | G | 1 | a0009c0103t0004g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3565-2748A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109219759 | ||||||
| chr12:109219760
|
C | T | 1 | a0002c0024t0003g0034 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3565-2747C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109219760 | ||||||
| chr12:109219996
|
G | A | 27 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(24): Show | 27 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.3565-2511G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109219996 | ||||||
| chr12:109220017
|
G | C | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3565-2490G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109220017 | ||||||
| chr12:109220036
|
T | A | 1 | a0012c0035t0004g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3565-2471T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109220036 | ||||||
| chr12:109220265
|
G | A | 61 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(58): Show | 61 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.3565-2242G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109220265 | ||||||
| chr12:109220386
|
G | A | 3 | a0001c0003t0002g0101a0001c0003t0002g0193a0002c0117t0003g0125 | 3 | HG01175.hp2 HG02698.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3565-2121G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109220386 | ||||||
| chr12:109220427
|
G | C | 1 | a0003c0081t0002g0230 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3565-2080G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109220427 | ||||||
| chr12:109220449
|
A | C | 1 | a0006c0113t0004g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3565-2058A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109220449 | ||||||
| chr12:109220453
|
C | T | 1 | a0001c0060t0002g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3565-2054C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109220453 | ||||||
| chr12:109220575
|
A | G | 24 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(21): Show | 24 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.3565-1932A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109220575 | ||||||
| chr12:109220738
|
G | A | 1 | a0002c0092t0010g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3565-1769G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109220738 | ||||||
| chr12:109221000
|
C | T | 1 | a0001c0038t0001g0029 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3565-1507C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221000 | ||||||
| chr12:109221138
|
C | A | 1 | a0032c0059t0002g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3565-1369C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221138 | ||||||
| chr12:109221193
|
T | C | 3 | a0033c0063t0010g0117a0035c0076t0010g0267a0039c0080t0010g0071 | 3 | HG03098.hp2 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3565-1314T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221193 | ||||||
| chr12:109221345
|
G | T | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3565-1162G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221345 | ||||||
| chr12:109221372
|
A | G | 49 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(46): Show | 49 | HG00323.hp1 HG01081.hp1 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.3565-1135A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221372 | ||||||
| chr12:109221645
|
G | A | 4 | a0006c0113t0004g0031a0033c0063t0010g0117a0035c0076t0010g0267others(1): Show | 4 | HG03098.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3565-862G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221645 | ||||||
| chr12:109221694
|
T | G | 7 | a0002c0043t0003g0012a0002c0061t0003g0062a0002c0086t0003g0260others(4): Show | 7 | HG01168.hp2 HG01261.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.3565-813T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221694 | ||||||
| chr12:109221879
|
C | CT | 14 | a0001c0002t0001g0079a0001c0002t0001g0091a0001c0002t0021g0243others(11): Show | 14 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.3565-613dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109221879 | |||||
| chr12:109221889
|
T | C | 1 | a0032c0059t0002g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3565-618T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221889 | ||||||
| chr12:109221893
|
T | G | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3565-614T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221893 | ||||||
| chr12:109221894
|
T | G | 9 | a0001c0046t0002g0067a0001c0046t0002g0190a0003c0001t0001g0143others(6): Show | 9 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.3565-613T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221894 | ||||||
| chr12:109221894
|
T | TTGG | 40 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(37): Show | 40 | HG00323.hp1 HG01081.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.3565-613_3565-612i others(5): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221894 | ||||||
| chr12:109221895
|
G | C | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3565-612G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221895 | ||||||
| chr12:109221899
|
G | C | 7 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3565-608G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221899 | ||||||
| chr12:109221936
|
A | G | 49 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(46): Show | 49 | HG00323.hp1 HG01081.hp1 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.3565-571A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221936 | ||||||
| chr12:109221978
|
G | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3565-529G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | chr12 | 109221978 | ||||||
| chr12:109222294
|
C | CGAGT | 13 | a0001c0011t0001g0008a0001c0039t0004g0039a0001c0039t0004g0116others(10): Show | 13 | HG00323.hp1 HG00323.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3565-194_3565-191d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109222294 | |||||
| chr12:109222294
|
C | CGAGTGAG others(5): Show |
17 | a0001c0003t0004g0074a0001c0016t0011g0274a0001c0069t0002g0204others(14): Show | 17 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.3565-202_3565-191d others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109222294 | |||||
| chr12:109222294
|
C | CGAGTGAG others(9): Show |
14 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0009g0186others(11): Show | 14 | HG01081.hp1 HG01106.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.3565-206_3565-191d others(18): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109222294 | |||||
| chr12:109222294
|
C | CGAGTGAG others(13): Show |
64 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(61): Show | 64 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.3565-210_3565-191d others(22): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109222294 | |||||
| chr12:109222294
|
C | CGAGTGAG others(17): Show |
5 | a0001c0010t0002g0261a0001c0013t0001g0153a0003c0001t0001g0064others(2): Show | 5 | HG01069.hp2 NA18951.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.3565-191_3565-190i others(26): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109222294 | |||||
| chr12:109222294
|
C | CGAGTGAG others(21): Show |
1 | a0001c0034t0001g0212 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3565-191_3565-190i others(30): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109222294 | |||||
| chr12:109222294
|
C | CGAGTGAG others(25): Show |
1 | a0001c0034t0001g0211 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3565-191_3565-190i others(34): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | 109222294 | |||||
| chr12:109222667
|
C | T | 3 | a0001c0004t0002g0054a0002c0007t0003g0055a0014c0077t0004g0118 | 3 | HG01884.hp2 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3678+47C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 25/52 | chr12 | 109222667 | ||||||
| chr12:109222685
|
C | T | 10 | a0002c0006t0005g0284a0002c0006t0005g0294a0002c0017t0024g0044others(7): Show | 10 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3678+65C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 25/52 | chr12 | 109222685 | ||||||
| chr12:109222724
|
C | T | 3 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3679-75C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 25/52 | chr12 | 109222724 | ||||||
| chr12:109222730
|
G | C | 1 | a0001c0023t0004g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3679-69G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 25/52 | chr12 | 109222730 | ||||||
| chr12:109222770
|
C | T | 1 | a0001c0003t0004g0074 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3679-29C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 25/52 | chr12 | 109222770 | ||||||
| chr12:109222773
|
C | T | 3 | a0001c0023t0001g0100a0001c0023t0001g0122a0002c0097t0003g0124 | 3 | HG01258.hp1 HG01515.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3679-26C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 25/52 | chr12 | 109222773 | ||||||
| chr12:109222793
|
C | T | 3 | a0002c0024t0003g0302a0003c0001t0001g0143a0004c0008t0001g0221 | 3 | HG00642.hp2 HG00741.hp2 HG01255.hp1 |
splice_region_variant&intron_variant | LOW | c.3679-6C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 25/52 | chr12 | 109222793 | ||||||
| chr12:109223130
|
G | A | 1 | a0001c0003t0002g0099 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3792+218G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 26/52 | chr12 | 109223130 | ||||||
| chr12:109223183
|
A | G | 1 | a0002c0017t0003g0042 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3792+271A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 26/52 | chr12 | 109223183 | ||||||
| chr12:109223514
|
C | T | 1 | a0007c0030t0004g0285 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3793-301C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 26/52 | chr12 | 109223514 | ||||||
| chr12:109223535
|
T | C | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3793-280T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 26/52 | chr12 | 109223535 | ||||||
| chr12:109223574
|
T | C | 1 | a0011c0027t0004g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3793-241T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 26/52 | chr12 | 109223574 | ||||||
| chr12:109223631
|
C | T | 1 | a0002c0110t0003g0268 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3793-184C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 26/52 | chr12 | 109223631 | ||||||
| chr12:109224174
|
T | C | 111 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(108): Show | 111 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.3882+270T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109224174 | ||||||
| chr12:109224189
|
A | G | 1 | a0003c0005t0002g0299 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3882+285A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109224189 | ||||||
| chr12:109224318
|
C | G | 1 | a0007c0057t0004g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3882+414C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109224318 | ||||||
| chr12:109224370
|
C | T | 13 | a0001c0003t0004g0074a0002c0017t0003g0042a0002c0043t0003g0012others(10): Show | 13 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.3882+466C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109224370 | ||||||
| chr12:109224447
|
G | A | 3 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3882+543G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109224447 | ||||||
| chr12:109224532
|
T | TTTA | 39 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0091others(36): Show | 39 | HG00642.hp2 HG00741.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.3882+649_3882+651d others(5): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | INFO_REALIGN_3_PRIME | chr12 | 109224532 | |||||
| chr12:109224532
|
T | TTTATTA | 25 | a0001c0016t0011g0274a0001c0039t0004g0039a0001c0064t0009g0184others(22): Show | 25 | HG00323.hp1 HG01891.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.3882+646_3882+651d others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | INFO_REALIGN_3_PRIME | chr12 | 109224532 | |||||
| chr12:109224652
|
C | T | 26 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0064t0009g0184others(23): Show | 26 | HG00323.hp1 HG01891.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.3882+748C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109224652 | ||||||
| chr12:109224660
|
T | C | 27 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(24): Show | 27 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.3882+756T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109224660 | ||||||
| chr12:109224714
|
T | C | 111 | a0001c0002t0001g0081a0001c0002t0001g0109a0001c0002t0001g0114others(108): Show | 111 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3882+810T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109224714 | ||||||
| chr12:109224831
|
A | ATGAGATG others(8): Show |
55 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(52): Show | 55 | HG00323.hp1 HG01069.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.3882+929_3882+930i others(17): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | INFO_REALIGN_3_PRIME | chr12 | 109224831 | |||||
| chr12:109224844
|
G | A | 23 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(20): Show | 23 | HG00323.hp1 HG01891.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.3882+940G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109224844 | ||||||
| chr12:109224926
|
T | C | 31 | a0001c0016t0011g0274a0001c0039t0004g0039a0001c0039t0004g0116others(28): Show | 31 | HG00323.hp1 HG01069.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.3882+1022T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109224926 | ||||||
| chr12:109225134
|
A | G | 2 | a0001c0002t0001g0035a0028c0100t0001g0070 | 2 | NA18980.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.3882+1230A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109225134 | ||||||
| chr12:109225183
|
A | G | 49 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(46): Show | 49 | HG00323.hp1 HG01081.hp1 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.3882+1279A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109225183 | ||||||
| chr12:109225287
|
T | TTGACTTA others(817): Show |
1 | a0006c0031t0013g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3882+1390_3882+139 others(828): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | INFO_REALIGN_3_PRIME | chr12 | 109225287 | |||||
| chr12:109225295
|
C | T | 115 | a0001c0002t0001g0035a0001c0002t0001g0126a0001c0002t0001g0191others(112): Show | 115 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.3882+1391C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109225295 | ||||||
| chr12:109225389
|
C | T | 4 | a0009c0096t0009g0295a0033c0063t0010g0117a0035c0076t0010g0267others(1): Show | 4 | HG03098.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3882+1485C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109225389 | ||||||
| chr12:109225513
|
G | A | 28 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(25): Show | 28 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.3882+1609G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109225513 | ||||||
| chr12:109225662
|
C | T | 2 | a0002c0014t0003g0113a0002c0014t0003g0303 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3883-1709C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109225662 | ||||||
| chr12:109225740
|
C | T | 5 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(2): Show | 5 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.3883-1631C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109225740 | ||||||
| chr12:109225741
|
G | A | 1 | a0006c0120t0003g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3883-1630G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109225741 | ||||||
| chr12:109225776
|
A | G | 117 | a0001c0002t0001g0035a0001c0002t0001g0126a0001c0002t0001g0191others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.3883-1595A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109225776 | ||||||
| chr12:109225808
|
A | T | 10 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0009g0186others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.3883-1563A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109225808 | ||||||
| chr12:109226384
|
C | T | 1 | a0027c0065t0005g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3883-987C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109226384 | ||||||
| chr12:109226466
|
A | G | 23 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(20): Show | 23 | HG00323.hp1 HG01891.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.3883-905A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109226466 | ||||||
| chr12:109226470
|
C | T | 1 | a0003c0005t0002g0264 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3883-901C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109226470 | ||||||
| chr12:109226614
|
G | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3883-757G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109226614 | ||||||
| chr12:109226699
|
C | CA | 110 | a0001c0002t0001g0035a0001c0002t0001g0126a0001c0002t0001g0191others(107): Show | 110 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.3883-652dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | INFO_REALIGN_3_PRIME | chr12 | 109226699 | |||||
| chr12:109226907
|
C | T | 38 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(35): Show | 38 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.3883-464C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109226907 | ||||||
| chr12:109226951
|
CT | C | 11 | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0022t0004g0004others(8): Show | 11 | HG01069.hp1 HG01433.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.3883-407delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | INFO_REALIGN_3_PRIME | chr12 | 109226951 | |||||
| chr12:109227015
|
A | G | 1 | a0004c0008t0008g0216 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3883-356A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109227015 | ||||||
| chr12:109227055
|
A | G | 28 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0074others(25): Show | 28 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.3883-316A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109227055 | ||||||
| chr12:109227062
|
C | T | 6 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(3): Show | 6 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.3883-309C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109227062 | ||||||
| chr12:109227314
|
T | C | 2 | a0007c0104t0004g0183a0015c0114t0004g0009 | 2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3883-57T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | chr12 | 109227314 | ||||||
| chr12:109227501
|
G | A | 1 | a0036c0094t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4001+12G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109227501 | ||||||
| chr12:109227644
|
C | T | 1 | a0001c0018t0011g0047 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4001+155C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109227644 | ||||||
| chr12:109227758
|
C | T | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4001+269C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109227758 | ||||||
| chr12:109227761
|
G | A | 3 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4001+272G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109227761 | ||||||
| chr12:109227794
|
G | A | 37 | a0001c0003t0004g0074a0001c0010t0009g0186a0001c0016t0009g0287others(34): Show | 37 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.4001+305G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109227794 | ||||||
| chr12:109227893
|
C | T | 4 | a0001c0002t0001g0085a0001c0011t0001g0008a0001c0050t0001g0277others(1): Show | 4 | HG00099.hp2 HG00323.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.4001+404C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109227893 | ||||||
| chr12:109227919
|
G | T | 17 | a0001c0003t0004g0074a0001c0064t0009g0184a0001c0069t0002g0204others(14): Show | 17 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.4001+430G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109227919 | ||||||
| chr12:109227974
|
C | T | 1 | a0023c0099t0001g0084 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.4001+485C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109227974 | ||||||
| chr12:109228003
|
C | T | 1 | a0001c0106t0001g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4001+514C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109228003 | ||||||
| chr12:109228033
|
C | CA | 9 | a0001c0002t0008g0306a0001c0004t0007g0020a0001c0016t0011g0274others(6): Show | 9 | HG02965.hp1 NA18952.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.4001+561dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | INFO_REALIGN_3_PRIME | chr12 | 109228033 | |||||
| chr12:109228033
|
C | CAA | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0074t0004g0229others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.4001+560_4001+561d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | INFO_REALIGN_3_PRIME | chr12 | 109228033 | |||||
| chr12:109228033
|
CA | C | 17 | a0001c0004t0020g0023a0001c0011t0001g0056a0001c0011t0001g0157others(14): Show | 17 | HG01109.hp2 HG01433.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.4001+561delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | INFO_REALIGN_3_PRIME | chr12 | 109228033 | |||||
| chr12:109228231
|
C | T | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4001+742C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109228231 | ||||||
| chr12:109228260
|
C | T | 2 | a0001c0124t0012g0197a0002c0092t0010g0192 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4001+771C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109228260 | ||||||
| chr12:109228578
|
A | G | 8 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.4001+1089A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109228578 | ||||||
| chr12:109228658
|
C | CA | 37 | a0001c0003t0004g0074a0001c0004t0002g0052a0001c0012t0002g0262others(34): Show | 37 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.4001+1189dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | INFO_REALIGN_3_PRIME | chr12 | 109228658 | |||||
| chr12:109228658
|
CA | C | 11 | a0001c0010t0002g0261a0001c0010t0009g0186a0001c0016t0009g0287others(8): Show | 11 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.4001+1189delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | INFO_REALIGN_3_PRIME | chr12 | 109228658 | |||||
| chr12:109228700
|
G | T | 8 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.4001+1211G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109228700 | ||||||
| chr12:109228964
|
A | AT | 4 | a0009c0096t0009g0295a0033c0063t0010g0117a0035c0076t0010g0267others(1): Show | 4 | HG03098.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4001+1478dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | INFO_REALIGN_3_PRIME | chr12 | 109228964 | |||||
| chr12:109228968
|
A | T | 4 | a0009c0096t0009g0295a0033c0063t0010g0117a0035c0076t0010g0267others(1): Show | 4 | HG03098.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4001+1479A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109228968 | ||||||
| chr12:109229003
|
G | A | 8 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.4001+1514G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229003 | ||||||
| chr12:109229088
|
G | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4001+1599G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229088 | ||||||
| chr12:109229194
|
T | C | 45 | a0001c0003t0004g0074a0001c0010t0009g0186a0001c0016t0009g0287others(42): Show | 45 | HG00323.hp1 HG01081.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.4001+1705T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229194 | ||||||
| chr12:109229277
|
C | A | 2 | a0001c0003t0002g0244a0003c0005t0002g0134 | 2 | HG02080.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.4001+1788C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229277 | ||||||
| chr12:109229326
|
C | G | 20 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0074t0004g0229others(17): Show | 20 | HG00323.hp1 HG01891.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.4001+1837C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229326 | ||||||
| chr12:109229358
|
C | T | 8 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.4001+1869C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229358 | ||||||
| chr12:109229359
|
G | A | 5 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(2): Show | 5 | HG02976.hp1 HG03139.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.4001+1870G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229359 | ||||||
| chr12:109229492
|
A | G | 3 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4001+2003A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229492 | ||||||
| chr12:109229523
|
G | C | 8 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.4001+2034G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229523 | ||||||
| chr12:109229591
|
G | A | 3 | a0001c0023t0001g0100a0001c0023t0001g0122a0002c0097t0003g0124 | 3 | HG01258.hp1 HG01515.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.4001+2102G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229591 | ||||||
| chr12:109229695
|
A | C | 16 | a0001c0003t0004g0074a0001c0064t0009g0184a0001c0069t0002g0204others(13): Show | 16 | HG01168.hp2 HG01261.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.4001+2206A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229695 | ||||||
| chr12:109229695
|
A | T | 1 | a0027c0065t0005g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4001+2206A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229695 | ||||||
| chr12:109229714
|
G | A | 7 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4001+2225G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229714 | ||||||
| chr12:109229942
|
T | G | 7 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4001+2453T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229942 | ||||||
| chr12:109229959
|
T | C | 2 | a0003c0083t0001g0151a0005c0019t0003g0152 | 2 | HG00735.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.4001+2470T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109229959 | ||||||
| chr12:109230115
|
C | A | 2 | a0004c0008t0008g0263a0008c0044t0003g0182 | 2 | NA18992.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.4002-2554C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230115 | ||||||
| chr12:109230234
|
C | G | 28 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(25): Show | 28 | HG00323.hp1 HG01891.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.4002-2435C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230234 | ||||||
| chr12:109230291
|
T | C | 17 | a0001c0003t0004g0074a0001c0064t0009g0184a0001c0069t0002g0204others(14): Show | 17 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.4002-2378T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230291 | ||||||
| chr12:109230372
|
T | C | 10 | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0022t0004g0004others(7): Show | 10 | HG01109.hp2 HG01433.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.4002-2297T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230372 | ||||||
| chr12:109230411
|
A | AATTCTTT others(1): Show |
129 | a0001c0002t0001g0035a0001c0002t0001g0126a0001c0002t0001g0191others(126): Show | 129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.4002-2258_4002-225 others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230411 | ||||||
| chr12:109230549
|
T | G | 1 | a0001c0003t0002g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4002-2120T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230549 | ||||||
| chr12:109230622
|
G | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4002-2047G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230622 | ||||||
| chr12:109230710
|
G | A | 1 | a0002c0021t0003g0252 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.4002-1959G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230710 | ||||||
| chr12:109230711
|
C | T | 17 | a0001c0003t0004g0074a0001c0064t0009g0184a0001c0069t0002g0204others(14): Show | 17 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.4002-1958C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230711 | ||||||
| chr12:109230777
|
G | T | 6 | a0001c0016t0009g0287a0001c0016t0009g0290a0001c0016t0009g0305others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.4002-1892G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230777 | ||||||
| chr12:109230799
|
T | C | 29 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(26): Show | 29 | HG00323.hp1 HG01891.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.4002-1870T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230799 | ||||||
| chr12:109230851
|
T | C | 1 | a0001c0069t0002g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4002-1818T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230851 | ||||||
| chr12:109230854
|
A | G | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4002-1815A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230854 | ||||||
| chr12:109230857
|
A | G | 1 | a0002c0061t0003g0062 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4002-1812A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230857 | ||||||
| chr12:109230964
|
G | A | 1 | a0005c0019t0003g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4002-1705G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230964 | ||||||
| chr12:109230987
|
G | A | 1 | a0001c0069t0002g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4002-1682G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109230987 | ||||||
| chr12:109231056
|
A | G | 1 | a0002c0017t0003g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4002-1613A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109231056 | ||||||
| chr12:109231079
|
C | T | 1 | a0004c0008t0008g0219 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.4002-1590C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109231079 | ||||||
| chr12:109231136
|
T | A | 10 | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0022t0004g0004others(7): Show | 10 | HG01109.hp2 HG01433.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.4002-1533T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109231136 | ||||||
| chr12:109231331
|
T | G | 13 | a0001c0003t0004g0074a0002c0017t0003g0042a0002c0043t0003g0012others(10): Show | 13 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.4002-1338T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109231331 | ||||||
| chr12:109231428
|
G | T | 1 | a0002c0020t0003g0120 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4002-1241G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109231428 | ||||||
| chr12:109231429
|
C | T | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4002-1240C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109231429 | ||||||
| chr12:109231506
|
G | A | 7 | a0001c0089t0002g0162a0002c0028t0003g0160a0002c0028t0003g0179others(4): Show | 7 | HG00609.hp1 HG02015.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.4002-1163G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109231506 | ||||||
| chr12:109231595
|
C | T | 6 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(3): Show | 6 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.4002-1074C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109231595 | ||||||
| chr12:109231625
|
C | T | 64 | a0001c0002t0001g0035a0001c0002t0001g0126a0001c0002t0001g0191others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.4002-1044C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109231625 | ||||||
| chr12:109231865
|
T | C | 126 | a0001c0002t0001g0035a0001c0002t0001g0126a0001c0002t0001g0191others(123): Show | 126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.4002-804T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109231865 | ||||||
| chr12:109231998
|
A | G | 3 | a0001c0003t0004g0074a0006c0113t0004g0031a0036c0094t0004g0072 | 3 | HG02922.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4002-671A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109231998 | ||||||
| chr12:109232424
|
C | T | 13 | a0001c0003t0004g0074a0001c0064t0009g0184a0002c0043t0003g0012others(10): Show | 13 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.4002-245C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109232424 | ||||||
| chr12:109232498
|
C | A | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4002-171C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109232498 | ||||||
| chr12:109232615
|
T | C | 1 | a0001c0004t0002g0052 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4002-54T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109232615 | ||||||
| chr12:109232663
|
T | C | 243 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
splice_region_variant&intron_variant | LOW | c.4002-6T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | chr12 | 109232663 | ||||||
| chr12:109232852
|
G | C | 95 | a0001c0002t0001g0081a0001c0002t0001g0085a0001c0002t0001g0109others(92): Show | 95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.4139+46G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 29/52 | chr12 | 109232852 | ||||||
| chr12:109232915
|
C | T | 1 | a0014c0077t0004g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4139+109C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 29/52 | chr12 | 109232915 | ||||||
| chr12:109232932
|
A | G | 1 | a0001c0003t0002g0104 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4139+126A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 29/52 | chr12 | 109232932 | ||||||
| chr12:109233021
|
A | G | 7 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4139+215A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 29/52 | chr12 | 109233021 | ||||||
| chr12:109233211
|
CAT | C | 13 | a0001c0003t0004g0074a0001c0064t0009g0184a0002c0043t0003g0012others(10): Show | 13 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.4139+408_4139+409d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 29/52 | INFO_REALIGN_3_PRIME | chr12 | 109233211 | |||||
| chr12:109233281
|
A | G | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4140-467A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 29/52 | chr12 | 109233281 | ||||||
| chr12:109233376
|
A | G | 6 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(3): Show | 6 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.4140-372A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 29/52 | chr12 | 109233376 | ||||||
| chr12:109233432
|
T | G | 2 | a0001c0003t0004g0074a0006c0113t0004g0031 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4140-316T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 29/52 | chr12 | 109233432 | ||||||
| chr12:109233595
|
A | T | 3 | a0033c0063t0010g0117a0035c0076t0010g0267a0039c0080t0010g0071 | 3 | HG03098.hp2 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4140-153A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 29/52 | chr12 | 109233595 | ||||||
| chr12:109233648
|
T | C | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4140-100T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 29/52 | chr12 | 109233648 | ||||||
| chr12:109233896
|
C | T | 34 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0085others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.4240-42C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 30/52 | chr12 | 109233896 | ||||||
| chr12:109233902
|
G | C | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4240-36G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 30/52 | chr12 | 109233902 | ||||||
| chr12:109233917
|
C | T | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4240-21C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 30/52 | chr12 | 109233917 | ||||||
| chr12:109233933
|
C | A | 34 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0085others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(31): Show |
splice_region_variant&intron_variant | LOW | c.4240-5C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 30/52 | chr12 | 109233933 | ||||||
| chr12:109234244
|
G | A | 33 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0085others(30): Show | 33 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.4347+199G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | chr12 | 109234244 | ||||||
| chr12:109234245
|
C | A | 2 | a0001c0002t0001g0126a0001c0108t0001g0010 | 2 | HG02258.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.4347+200C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | chr12 | 109234245 | ||||||
| chr12:109234250
|
G | A | 1 | a0001c0069t0002g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4347+205G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | chr12 | 109234250 | ||||||
| chr12:109234305
|
C | T | 1 | a0002c0006t0014g0080 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4347+260C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | chr12 | 109234305 | ||||||
| chr12:109234306
|
G | A | 5 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4347+261G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | chr12 | 109234306 | ||||||
| chr12:109234403
|
T | C | 6 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(3): Show | 6 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.4347+358T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | chr12 | 109234403 | ||||||
| chr12:109234518
|
T | C | 2 | a0001c0004t0017g0003a0006c0121t0004g0170 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4347+473T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | chr12 | 109234518 | ||||||
| chr12:109234738
|
G | C | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4348-575G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | chr12 | 109234738 | ||||||
| chr12:109234798
|
C | T | 1 | a0006c0026t0016g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4348-515C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | chr12 | 109234798 | ||||||
| chr12:109234812
|
C | T | 10 | a0002c0006t0005g0284a0002c0006t0005g0294a0002c0017t0024g0044others(7): Show | 10 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.4348-501C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | chr12 | 109234812 | ||||||
| chr12:109234935
|
G | GA | 34 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0085others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.4348-371dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | INFO_REALIGN_3_PRIME | chr12 | 109234935 | |||||
| chr12:109235011
|
A | G | 1 | a0001c0069t0002g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4348-302A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | chr12 | 109235011 | ||||||
| chr12:109235146
|
T | G | 95 | a0001c0002t0001g0081a0001c0002t0001g0109a0001c0002t0001g0114others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.4348-167T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | chr12 | 109235146 | ||||||
| chr12:109235272
|
G | A | 1 | a0006c0026t0016g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4348-41G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | chr12 | 109235272 | ||||||
| chr12:109235500
|
C | T | 1 | a0034c0102t0018g0195 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4405-106C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 32/52 | chr12 | 109235500 | ||||||
| chr12:109235683
|
G | A | 1 | a0039c0080t0010g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4446+36G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 33/52 | chr12 | 109235683 | ||||||
| chr12:109235720
|
G | A | 8 | a0001c0003t0002g0099a0001c0010t0002g0261a0002c0006t0014g0080others(5): Show | 8 | HG00423.hp2 HG02015.hp1 NA18984.hp2 others(5): Show |
intron_variant | MODIFIER | c.4446+73G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 33/52 | chr12 | 109235720 | ||||||
| chr12:109235781
|
T | A | 40 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0085others(37): Show | 40 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.4446+134T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 33/52 | chr12 | 109235781 | ||||||
| chr12:109236069
|
C | T | 5 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4446+422C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 33/52 | chr12 | 109236069 | ||||||
| chr12:109236122
|
G | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4446+475G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 33/52 | chr12 | 109236122 | ||||||
| chr12:109236122
|
G | T | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4446+475G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 33/52 | chr12 | 109236122 | ||||||
| chr12:109236401
|
G | A | 1 | a0001c0012t0002g0259 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.4446+754G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 33/52 | chr12 | 109236401 | ||||||
| chr12:109236744
|
A | AT | 11 | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0022t0004g0004others(8): Show | 11 | HG01109.hp2 HG01433.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.4447-411dupT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 33/52 | INFO_REALIGN_3_PRIME | chr12 | 109236744 | |||||
| chr12:109236792
|
G | C | 34 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0085others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.4447-373G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 33/52 | chr12 | 109236792 | ||||||
| chr12:109237004
|
G | A | 1 | a0006c0113t0004g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4447-161G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 33/52 | chr12 | 109237004 | ||||||
| chr12:109237460
|
G | T | 1 | a0002c0007t0003g0026 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.4662+80G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109237460 | ||||||
| chr12:109237787
|
G | A | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4662+407G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109237787 | ||||||
| chr12:109237880
|
C | T | 1 | a0033c0063t0010g0117 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4662+500C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109237880 | ||||||
| chr12:109237912
|
C | T | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4662+532C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109237912 | ||||||
| chr12:109238011
|
C | CA | 24 | a0001c0002t0001g0191a0001c0002t0001g0235a0001c0011t0008g0018others(21): Show | 24 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.4662+647dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | INFO_REALIGN_3_PRIME | chr12 | 109238011 | |||||
| chr12:109238058
|
A | G | 1 | a0011c0027t0013g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4662+678A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109238058 | ||||||
| chr12:109238242
|
A | G | 2 | a0001c0002t0001g0085a0001c0050t0001g0277 | 2 | HG00099.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.4662+862A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109238242 | ||||||
| chr12:109238342
|
AT | A | 18 | a0001c0003t0002g0068a0001c0013t0001g0237a0002c0014t0003g0015others(15): Show | 18 | HG01074.hp2 HG01106.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.4662+978delT | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | INFO_REALIGN_3_PRIME | chr12 | 109238342 | |||||
| chr12:109238396
|
A | G | 1 | a0003c0001t0001g0154 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.4662+1016A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109238396 | ||||||
| chr12:109238404
|
A | T | 7 | a0006c0122t0004g0167a0009c0025t0001g0105a0009c0025t0001g0269others(4): Show | 7 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.4662+1024A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109238404 | ||||||
| chr12:109238427
|
ATATAT | A | 5 | a0002c0006t0005g0294a0008c0015t0005g0171a0008c0015t0005g0172others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4662+1053_4662+105 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | INFO_REALIGN_3_PRIME | chr12 | 109238427 | |||||
| chr12:109238471
|
AAT | A | 157 | a0001c0002t0001g0035a0001c0002t0001g0081a0001c0002t0001g0109others(154): Show | 157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.4662+1094_4662+109 others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | INFO_REALIGN_3_PRIME | chr12 | 109238471 | |||||
| chr12:109238521
|
T | C | 1 | a0014c0077t0004g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4662+1141T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109238521 | ||||||
| chr12:109238563
|
A | G | 1 | a0002c0014t0003g0015 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4662+1183A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109238563 | ||||||
| chr12:109238570
|
TA | T | 11 | a0001c0010t0002g0021a0001c0012t0002g0045a0001c0012t0002g0250others(8): Show | 11 | HG00673.hp1 HG02040.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.4662+1191delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109238570 | ||||||
| chr12:109238573
|
A | T | 152 | a0001c0002t0001g0035a0001c0002t0001g0081a0001c0002t0001g0109others(149): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.4662+1193A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109238573 | ||||||
| chr12:109238621
|
A | G | 12 | a0001c0003t0004g0300a0001c0060t0002g0272a0002c0006t0005g0284others(9): Show | 12 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.4663-1209A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109238621 | ||||||
| chr12:109238697
|
C | T | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4663-1133C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109238697 | ||||||
| chr12:109238781
|
T | G | 5 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4663-1049T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109238781 | ||||||
| chr12:109238792
|
C | T | 1 | a0014c0077t0004g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4663-1038C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109238792 | ||||||
| chr12:109239019
|
C | G | 3 | a0033c0063t0010g0117a0035c0076t0010g0267a0039c0080t0010g0071 | 3 | HG03098.hp2 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4663-811C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109239019 | ||||||
| chr12:109239362
|
G | A | 3 | a0033c0063t0010g0117a0035c0076t0010g0267a0039c0080t0010g0071 | 3 | HG03098.hp2 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4663-468G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109239362 | ||||||
| chr12:109239538
|
C | T | 12 | a0001c0003t0004g0074a0002c0043t0003g0012a0002c0061t0003g0062others(9): Show | 12 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.4663-292C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | 109239538 | ||||||
| chr12:109240432
|
A | G | 12 | a0001c0003t0004g0074a0002c0043t0003g0012a0002c0061t0003g0062others(9): Show | 12 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.4818+447A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 35/52 | chr12 | 109240432 | ||||||
| chr12:109240465
|
T | C | 7 | a0006c0122t0004g0167a0009c0025t0001g0105a0009c0025t0001g0269others(4): Show | 7 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.4818+480T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 35/52 | chr12 | 109240465 | ||||||
| chr12:109240671
|
C | T | 1 | a0001c0023t0004g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4819-407C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 35/52 | chr12 | 109240671 | ||||||
| chr12:109240684
|
G | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4819-394G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 35/52 | chr12 | 109240684 | ||||||
| chr12:109240821
|
TCA | T | 11 | a0001c0003t0004g0074a0002c0043t0003g0012a0002c0061t0003g0062others(8): Show | 11 | HG01168.hp2 HG01261.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.4819-256_4819-255d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 35/52 | chr12 | 109240821 | ||||||
| chr12:109240858
|
T | C | 1 | a0004c0040t0002g0213 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4819-220T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 35/52 | chr12 | 109240858 | ||||||
| chr12:109240873
|
A | G | 1 | a0027c0065t0005g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4819-205A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 35/52 | chr12 | 109240873 | ||||||
| chr12:109240879
|
G | A | 2 | a0001c0011t0001g0008a0009c0096t0009g0295 | 2 | HG00323.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4819-199G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 35/52 | chr12 | 109240879 | ||||||
| chr12:109240921
|
G | A | 1 | a0006c0026t0002g0155 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4819-157G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 35/52 | chr12 | 109240921 | ||||||
| chr12:109240941
|
A | G | 1 | a0014c0077t0004g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4819-137A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 35/52 | chr12 | 109240941 | ||||||
| chr12:109241296
|
C | T | 1 | a0002c0006t0003g0095 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5022+15C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/52 | chr12 | 109241296 | ||||||
| chr12:109241331
|
G | T | 12 | a0001c0003t0004g0074a0002c0043t0003g0012a0002c0061t0003g0062others(9): Show | 12 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.5022+50G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/52 | chr12 | 109241331 | ||||||
| chr12:109241568
|
G | A | 1 | a0007c0030t0004g0280 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5022+287G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/52 | chr12 | 109241568 | ||||||
| chr12:109241627
|
G | A | 1 | a0001c0048t0002g0281 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5022+346G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/52 | chr12 | 109241627 | ||||||
| chr12:109241741
|
G | C | 1 | a0008c0015t0005g0173 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5022+460G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/52 | chr12 | 109241741 | ||||||
| chr12:109241836
|
G | A | 1 | a0002c0024t0003g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.5022+555G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/52 | chr12 | 109241836 | ||||||
| chr12:109241838
|
C | A | 12 | a0001c0111t0001g0275a0002c0014t0003g0106a0002c0021t0003g0252others(9): Show | 12 | HG00735.hp1 HG01109.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.5022+557C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/52 | chr12 | 109241838 | ||||||
| chr12:109241842
|
T | C | 5 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.5022+561T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/52 | chr12 | 109241842 | ||||||
| chr12:109242198
|
T | A | 179 | a0001c0002t0001g0035a0001c0002t0001g0081a0001c0002t0001g0109others(176): Show | 179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.5023-239T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/52 | chr12 | 109242198 | ||||||
| chr12:109242282
|
A | G | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5023-155A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/52 | chr12 | 109242282 | ||||||
| chr12:109242295
|
G | A | 8 | a0001c0004t0002g0052a0001c0004t0007g0001a0001c0004t0007g0011others(5): Show | 9 | HG00597.hp1 HG02083.hp1 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.5023-142G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/52 | chr12 | 109242295 | ||||||
| chr12:109242330
|
A | G | 1 | a0032c0059t0002g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5023-107A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/52 | chr12 | 109242330 | ||||||
| chr12:109242422
|
T | C | 3 | a0033c0063t0010g0117a0035c0076t0010g0267a0039c0080t0010g0071 | 3 | HG03098.hp2 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5023-15T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 36/52 | chr12 | 109242422 | ||||||
| chr12:109242761
|
G | C | 2 | a0017c0123t0015g0058a0026c0066t0015g0115 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.5178+169G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109242761 | ||||||
| chr12:109243076
|
T | C | 8 | a0001c0045t0002g0146a0001c0087t0001g0236a0002c0007t0006g0017others(5): Show | 8 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.5178+484T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109243076 | ||||||
| chr12:109243444
|
C | T | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5178+852C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109243444 | ||||||
| chr12:109243726
|
A | G | 1 | a0019c0093t0001g0159 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.5178+1134A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109243726 | ||||||
| chr12:109243855
|
C | A | 2 | a0001c0124t0012g0197a0002c0092t0010g0192 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5178+1263C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109243855 | ||||||
| chr12:109243877
|
T | TTATATAT others(21): Show |
1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5178+1304_5178+130 others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | INFO_REALIGN_3_PRIME | chr12 | 109243877 | |||||
| chr12:109243879
|
A | G | 7 | a0006c0122t0004g0167a0009c0025t0001g0105a0009c0025t0001g0269others(4): Show | 7 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.5178+1287A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109243879 | ||||||
| chr12:109243889
|
A | ATATT | 6 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.5178+1300_5178+130 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | INFO_REALIGN_3_PRIME | chr12 | 109243889 | |||||
| chr12:109243893
|
A | ATT | 87 | a0001c0002t0001g0081a0001c0002t0001g0109a0001c0002t0001g0114others(84): Show | 87 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.5178+1302_5178+130 others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | INFO_REALIGN_3_PRIME | chr12 | 109243893 | |||||
| chr12:109243893
|
A | T | 136 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.5178+1301A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109243893 | ||||||
| chr12:109243897
|
T | A | 2 | a0001c0064t0009g0184a0009c0096t0009g0295 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.5178+1305T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109243897 | ||||||
| chr12:109244363
|
T | C | 5 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.5179-1263T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109244363 | ||||||
| chr12:109244373
|
TCA | T | 7 | a0001c0089t0002g0162a0002c0028t0003g0160a0002c0028t0003g0179others(4): Show | 7 | HG00609.hp1 HG02015.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.5179-1252_5179-125 others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109244373 | ||||||
| chr12:109244551
|
G | A | 63 | a0001c0002t0001g0035a0001c0002t0001g0126a0001c0002t0001g0191others(60): Show | 63 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.5179-1075G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109244551 | ||||||
| chr12:109244562
|
G | A | 1 | a0002c0014t0003g0106 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5179-1064G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109244562 | ||||||
| chr12:109244630
|
T | G | 1 | a0001c0004t0002g0052 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.5179-996T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109244630 | ||||||
| chr12:109244673
|
G | T | 1 | a0021c0068t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5179-953G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109244673 | ||||||
| chr12:109244685
|
C | T | 5 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.5179-941C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109244685 | ||||||
| chr12:109244755
|
GCTGT | G | 9 | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0022t0004g0004others(6): Show | 9 | HG01433.hp1 HG02630.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.5179-855_5179-852d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | INFO_REALIGN_3_PRIME | chr12 | 109244755 | |||||
| chr12:109244820
|
A | C | 2 | a0001c0124t0012g0197a0002c0092t0010g0192 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5179-806A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109244820 | ||||||
| chr12:109244921
|
C | T | 1 | a0003c0001t0001g0147 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.5179-705C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109244921 | ||||||
| chr12:109245125
|
G | A | 158 | a0001c0002t0001g0035a0001c0002t0001g0081a0001c0002t0001g0109others(155): Show | 158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.5179-501G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109245125 | ||||||
| chr12:109245250
|
G | A | 1 | a0001c0003t0002g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5179-376G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109245250 | ||||||
| chr12:109245254
|
T | C | 227 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(224): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.5179-372T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109245254 | ||||||
| chr12:109245303
|
A | G | 1 | a0018c0051t0023g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5179-323A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109245303 | ||||||
| chr12:109245392
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.5179-234C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109245392 | ||||||
| chr12:109245397
|
C | A | 1 | a0001c0108t0001g0010 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5179-229C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109245397 | ||||||
| chr12:109245516
|
G | A | 8 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.5179-110G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | 109245516 | ||||||
| chr12:109245770
|
A | G | 186 | a0001c0002t0001g0035a0001c0002t0001g0081a0001c0002t0001g0109others(183): Show | 186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.5301+22A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 38/52 | chr12 | 109245770 | ||||||
| chr12:109245791
|
C | T | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5301+43C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 38/52 | chr12 | 109245791 | ||||||
| chr12:109245822
|
C | T | 1 | a0001c0048t0002g0281 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5301+74C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 38/52 | chr12 | 109245822 | ||||||
| chr12:109245890
|
A | G | 118 | a0001c0002t0001g0109a0001c0002t0001g0114a0001c0002t0001g0241others(115): Show | 118 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.5301+142A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 38/52 | chr12 | 109245890 | ||||||
| chr12:109246066
|
C | T | 4 | a0009c0025t0001g0105a0009c0025t0001g0269a0009c0025t0001g0270others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.5302-113C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 38/52 | chr12 | 109246066 | ||||||
| chr12:109246134
|
C | G | 1 | a0001c0060t0002g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5302-45C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 38/52 | chr12 | 109246134 | ||||||
| chr12:109246160
|
G | A | 10 | a0001c0011t0001g0056a0001c0022t0004g0004a0001c0022t0004g0005others(7): Show | 10 | HG01109.hp2 HG01433.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.5302-19G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 38/52 | chr12 | 109246160 | ||||||
| chr12:109246452
|
C | T | 2 | a0001c0124t0012g0197a0006c0031t0013g0205 | 2 | HG03453.hp2 NA20300.hp2 |
splice_region_variant&intron_variant | LOW | c.5571+4C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | chr12 | 109246452 | ||||||
| chr12:109246727
|
G | A | 8 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(5): Show | 8 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.5571+279G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | chr12 | 109246727 | ||||||
| chr12:109246793
|
A | G | 1 | a0002c0017t0003g0042 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5571+345A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | chr12 | 109246793 | ||||||
| chr12:109246906
|
G | A | 1 | a0001c0002t0001g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5571+458G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | chr12 | 109246906 | ||||||
| chr12:109246929
|
G | A | 4 | a0007c0030t0002g0110a0007c0101t0002g0086a0018c0051t0023g0279others(1): Show | 4 | HG02145.hp1 HG03654.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.5571+481G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | chr12 | 109246929 | ||||||
| chr12:109246955
|
T | C | 1 | a0017c0123t0015g0058 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5571+507T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | chr12 | 109246955 | ||||||
| chr12:109246995
|
T | C | 2 | a0001c0012t0002g0259a0004c0041t0002g0224 | 2 | NA18988.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.5571+547T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | chr12 | 109246995 | ||||||
| chr12:109247162
|
G | A | 1 | a0002c0006t0003g0095 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5572-444G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | chr12 | 109247162 | ||||||
| chr12:109247288
|
G | T | 223 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.5572-318G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | chr12 | 109247288 | ||||||
| chr12:109247311
|
A | G | 112 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0003t0002g0077others(109): Show | 113 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.5572-295A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | chr12 | 109247311 | ||||||
| chr12:109247525
|
G | A | 76 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0003t0002g0077others(73): Show | 77 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.5572-81G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | chr12 | 109247525 | ||||||
| chr12:109247533
|
C | T | 9 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.5572-73C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | chr12 | 109247533 | ||||||
| chr12:109247539
|
GA | G | 15 | a0001c0003t0004g0074a0001c0003t0004g0300a0001c0004t0017g0003others(12): Show | 15 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.5572-57delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | INFO_REALIGN_3_PRIME | chr12 | 109247539 | |||||
| chr12:109247740
|
A | G | 224 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.5669+37A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109247740 | ||||||
| chr12:109248104
|
T | C | 12 | a0002c0006t0005g0123a0002c0006t0005g0284a0002c0006t0005g0294others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.5669+401T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109248104 | ||||||
| chr12:109248108
|
T | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5669+405T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109248108 | ||||||
| chr12:109248160
|
T | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5669+457T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109248160 | ||||||
| chr12:109248501
|
CCTGGCAA others(4): Show |
C | 78 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0003t0002g0077others(75): Show | 79 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.5669+804_5669+814d others(13): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | INFO_REALIGN_3_PRIME | chr12 | 109248501 | |||||
| chr12:109248572
|
G | A | 1 | a0001c0109t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5669+869G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109248572 | ||||||
| chr12:109248605
|
G | A | 78 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0003t0002g0077others(75): Show | 79 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.5669+902G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109248605 | ||||||
| chr12:109248627
|
C | T | 4 | a0002c0092t0010g0192a0033c0063t0010g0117a0035c0076t0010g0267others(1): Show | 4 | HG03098.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.5669+924C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109248627 | ||||||
| chr12:109248916
|
T | C | 219 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.5670-1068T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109248916 | ||||||
| chr12:109248977
|
G | C | 90 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.5670-1007G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109248977 | ||||||
| chr12:109249108
|
A | G | 4 | a0002c0092t0010g0192a0033c0063t0010g0117a0035c0076t0010g0267others(1): Show | 4 | HG03098.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.5670-876A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109249108 | ||||||
| chr12:109249127
|
G | A | 1 | a0001c0029t0002g0108 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5670-857G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109249127 | ||||||
| chr12:109249140
|
A | G | 219 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.5670-844A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109249140 | ||||||
| chr12:109249281
|
G | C | 6 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.5670-703G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109249281 | ||||||
| chr12:109249369
|
C | G | 1 | a0001c0050t0001g0278 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5670-615C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109249369 | ||||||
| chr12:109249522
|
C | T | 2 | a0001c0003t0002g0112a0004c0040t0002g0213 | 2 | HG03490.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.5670-462C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109249522 | ||||||
| chr12:109249587
|
G | A | 1 | a0001c0062t0019g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5670-397G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109249587 | ||||||
| chr12:109249679
|
A | G | 1 | a0001c0109t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5670-305A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109249679 | ||||||
| chr12:109249882
|
A | G | 1 | a0010c0073t0014g0208 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.5670-102A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 40/52 | chr12 | 109249882 | ||||||
| chr12:109250241
|
A | G | 1 | a0001c0108t0001g0010 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5790+137A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109250241 | ||||||
| chr12:109250332
|
C | T | 3 | a0007c0030t0002g0110a0007c0101t0002g0086a0038c0082t0002g0127 | 3 | HG02145.hp1 HG03654.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.5790+228C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109250332 | ||||||
| chr12:109250379
|
G | A | 1 | a0001c0003t0002g0097 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5790+275G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109250379 | ||||||
| chr12:109250784
|
C | T | 237 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.5790+680C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109250784 | ||||||
| chr12:109250831
|
A | G | 1 | a0039c0080t0010g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5790+727A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109250831 | ||||||
| chr12:109250919
|
C | T | 1 | a0006c0120t0003g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5790+815C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109250919 | ||||||
| chr12:109251077
|
G | A | 4 | a0002c0092t0010g0192a0033c0063t0010g0117a0035c0076t0010g0267others(1): Show | 4 | HG03098.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.5791-969G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109251077 | ||||||
| chr12:109251241
|
C | G | 69 | a0001c0003t0002g0068a0001c0003t0002g0077a0001c0003t0002g0078others(66): Show | 69 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.5791-805C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109251241 | ||||||
| chr12:109251538
|
G | A | 2 | a0003c0005t0002g0129a0024c0091t0002g0174 | 2 | HG00408.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.5791-508G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109251538 | ||||||
| chr12:109251587
|
T | TC | 7 | a0001c0004t0007g0001a0001c0004t0007g0011a0001c0004t0007g0019others(4): Show | 8 | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.5791-455dupC | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | INFO_REALIGN_3_PRIME | chr12 | 109251587 | |||||
| chr12:109251588
|
C | T | 95 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.5791-458C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109251588 | ||||||
| chr12:109251609
|
C | T | 1 | a0001c0074t0004g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5791-437C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109251609 | ||||||
| chr12:109251622
|
C | T | 1 | a0001c0029t0011g0090 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.5791-424C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109251622 | ||||||
| chr12:109251775
|
C | A | 1 | a0004c0112t0001g0119 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.5791-271C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109251775 | ||||||
| chr12:109251923
|
C | T | 3 | a0001c0004t0002g0054a0001c0060t0002g0272a0001c0107t0012g0196 | 3 | HG02109.hp1 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5791-123C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | chr12 | 109251923 | ||||||
| chr12:109252192
|
G | A | 12 | a0001c0003t0004g0074a0001c0003t0004g0300a0001c0004t0017g0003others(9): Show | 12 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.5901+36G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 42/52 | chr12 | 109252192 | ||||||
| chr12:109252215
|
T | G | 1 | a0001c0050t0001g0277 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.5901+59T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 42/52 | chr12 | 109252215 | ||||||
| chr12:109252322
|
G | GA | 7 | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0055t0001g0226others(4): Show | 7 | HG02630.hp1 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.5901+176dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 42/52 | INFO_REALIGN_3_PRIME | chr12 | 109252322 | |||||
| chr12:109252355
|
G | A | 1 | a0003c0001t0001g0154 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.5901+199G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 42/52 | chr12 | 109252355 | ||||||
| chr12:109252440
|
CA | C | 84 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.5901+290delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 42/52 | INFO_REALIGN_3_PRIME | chr12 | 109252440 | |||||
| chr12:109252509
|
A | T | 70 | a0001c0003t0002g0068a0001c0003t0002g0077a0001c0003t0002g0078others(67): Show | 70 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.5901+353A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 42/52 | chr12 | 109252509 | ||||||
| chr12:109252593
|
T | C | 1 | a0001c0087t0001g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5902-422T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 42/52 | chr12 | 109252593 | ||||||
| chr12:109252620
|
C | T | 4 | a0002c0092t0010g0192a0033c0063t0010g0117a0035c0076t0010g0267others(1): Show | 4 | HG03098.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902-395C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 42/52 | chr12 | 109252620 | ||||||
| chr12:109252782
|
T | C | 1 | a0003c0001t0001g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.5902-233T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 42/52 | chr12 | 109252782 | ||||||
| chr12:109253193
|
G | A | 4 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(1): Show | 4 | HG02109.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.6045+35G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 43/52 | chr12 | 109253193 | ||||||
| chr12:109253209
|
A | G | 1 | a0003c0001t0001g0145 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.6045+51A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 43/52 | chr12 | 109253209 | ||||||
| chr12:109253633
|
G | A | 3 | a0001c0023t0004g0121a0001c0034t0001g0211a0001c0034t0001g0212 | 3 | HG00099.hp1 HG00280.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.6045+475G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 43/52 | chr12 | 109253633 | ||||||
| chr12:109253797
|
C | A | 2 | a0017c0123t0015g0058a0026c0066t0015g0115 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.6046-417C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 43/52 | chr12 | 109253797 | ||||||
| chr12:109253867
|
T | C | 114 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.6046-347T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 43/52 | chr12 | 109253867 | ||||||
| chr12:109254186
|
A | G | 214 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.6046-28A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 43/52 | chr12 | 109254186 | ||||||
| chr12:109254385
|
G | GGCTTGAG others(24): Show |
16 | a0002c0006t0005g0123a0002c0006t0005g0284a0002c0006t0005g0294others(13): Show | 16 | HG01081.hp1 HG01167.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.6166+66_6166+96dup others(31): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | INFO_REALIGN_3_PRIME | chr12 | 109254385 | |||||
| chr12:109254438
|
T | C | 2 | a0002c0007t0022g0032a0010c0042t0003g0220 | 2 | HG01167.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.6166+104T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109254438 | ||||||
| chr12:109254444
|
C | A | 1 | a0002c0024t0003g0302 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.6166+110C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109254444 | ||||||
| chr12:109254726
|
C | G | 8 | a0001c0029t0011g0090a0003c0005t0002g0129a0003c0005t0002g0240others(5): Show | 8 | HG00408.hp1 HG02132.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.6166+392C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109254726 | ||||||
| chr12:109254837
|
C | T | 6 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(3): Show | 6 | HG02976.hp1 HG03139.hp1 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.6166+503C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109254837 | ||||||
| chr12:109254865
|
C | T | 3 | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0055t0001g0226 | 3 | HG02630.hp1 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.6166+531C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109254865 | ||||||
| chr12:109254963
|
C | T | 1 | a0001c0062t0019g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6166+629C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109254963 | ||||||
| chr12:109255001
|
A | G | 221 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.6166+667A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109255001 | ||||||
| chr12:109255095
|
T | TAC | 5 | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0048t0004g0307others(2): Show | 5 | HG02630.hp1 HG02922.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.6166+782_6166+783d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | INFO_REALIGN_3_PRIME | chr12 | 109255095 | |||||
| chr12:109255095
|
T | TACAC | 3 | a0033c0063t0010g0117a0035c0076t0010g0267a0039c0080t0010g0071 | 3 | HG03098.hp2 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.6166+780_6166+783d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | INFO_REALIGN_3_PRIME | chr12 | 109255095 | |||||
| chr12:109255129
|
C | T | 15 | a0001c0003t0004g0074a0001c0003t0004g0300a0001c0004t0017g0003others(12): Show | 15 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.6166+795C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109255129 | ||||||
| chr12:109255173
|
T | G | 1 | a0001c0064t0009g0184 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6166+839T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109255173 | ||||||
| chr12:109255231
|
A | C | 13 | a0002c0006t0005g0123a0002c0006t0005g0284a0002c0006t0005g0294others(10): Show | 13 | HG01081.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.6166+897A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109255231 | ||||||
| chr12:109255353
|
G | A | 1 | a0001c0048t0004g0307 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6167-787G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109255353 | ||||||
| chr12:109255503
|
C | T | 2 | a0011c0027t0004g0150a0011c0027t0013g0065 | 2 | HG01168.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.6167-637C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109255503 | ||||||
| chr12:109255540
|
G | T | 1 | a0025c0090t0003g0130 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.6167-600G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109255540 | ||||||
| chr12:109255543
|
G | A | 7 | a0001c0010t0001g0188a0003c0083t0001g0151a0009c0025t0001g0105others(4): Show | 7 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.6167-597G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109255543 | ||||||
| chr12:109255552
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6167-588A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109255552 | ||||||
| chr12:109255561
|
A | T | 1 | a0002c0006t0005g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.6167-579A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109255561 | ||||||
| chr12:109255604
|
C | T | 1 | a0003c0001t0001g0265 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6167-536C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109255604 | ||||||
| chr12:109255610
|
C | T | 2 | a0001c0064t0009g0184a0009c0096t0009g0295 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.6167-530C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109255610 | ||||||
| chr12:109256076
|
G | A | 1 | a0002c0007t0003g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6167-64G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | chr12 | 109256076 | ||||||
| chr12:109256425
|
T | G | 65 | a0001c0003t0002g0068a0001c0003t0002g0077a0001c0003t0002g0078others(62): Show | 65 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.6263+189T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109256425 | ||||||
| chr12:109256515
|
C | A | 70 | a0001c0003t0002g0068a0001c0003t0002g0077a0001c0003t0002g0078others(67): Show | 70 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.6263+279C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109256515 | ||||||
| chr12:109256521
|
A | G | 6 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.6263+285A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109256521 | ||||||
| chr12:109256757
|
T | C | 1 | a0001c0045t0002g0146 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.6263+521T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109256757 | ||||||
| chr12:109256797
|
C | T | 2 | a0001c0087t0001g0236a0003c0001t0001g0087 | 2 | HG00438.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.6263+561C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109256797 | ||||||
| chr12:109256961
|
T | C | 6 | a0001c0010t0001g0188a0003c0083t0001g0151a0009c0025t0001g0105others(3): Show | 6 | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.6263+725T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109256961 | ||||||
| chr12:109257187
|
T | A | 1 | a0001c0002t0001g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.6263+951T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109257187 | ||||||
| chr12:109257261
|
G | A | 22 | a0001c0022t0004g0004a0001c0022t0004g0005a0001c0022t0004g0006others(19): Show | 22 | HG01168.hp2 HG01261.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.6264-1007G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109257261 | ||||||
| chr12:109257289
|
A | G | 4 | a0002c0092t0010g0192a0033c0063t0010g0117a0035c0076t0010g0267others(1): Show | 4 | HG03098.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.6264-979A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109257289 | ||||||
| chr12:109257319
|
TA | T | 12 | a0001c0003t0002g0078a0001c0010t0009g0186a0001c0016t0009g0287others(9): Show | 12 | HG02080.hp2 HG02109.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.6264-936delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | INFO_REALIGN_3_PRIME | chr12 | 109257319 | |||||
| chr12:109257324
|
A | T | 1 | a0002c0088t0006g0247 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.6264-944A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109257324 | ||||||
| chr12:109257523
|
C | T | 2 | a0017c0123t0015g0058a0026c0066t0015g0115 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.6264-745C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109257523 | ||||||
| chr12:109257786
|
G | A | 1 | a0002c0117t0003g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6264-482G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109257786 | ||||||
| chr12:109257796
|
C | G | 2 | a0002c0014t0003g0106a0010c0042t0003g0209 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.6264-472C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109257796 | ||||||
| chr12:109258016
|
G | T | 1 | a0007c0030t0004g0280 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6264-252G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109258016 | ||||||
| chr12:109258086
|
A | G | 57 | a0001c0003t0002g0068a0001c0003t0002g0078a0001c0003t0002g0094others(54): Show | 57 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.6264-182A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109258086 | ||||||
| chr12:109258200
|
C | A | 1 | a0006c0113t0004g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6264-68C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | chr12 | 109258200 | ||||||
| chr12:109258384
|
T | A | 1 | a0001c0029t0002g0108 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6360+20T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 46/52 | chr12 | 109258384 | ||||||
| chr12:109258429
|
C | T | 2 | a0017c0123t0015g0058a0026c0066t0015g0115 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.6360+65C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 46/52 | chr12 | 109258429 | ||||||
| chr12:109258430
|
G | A | 7 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.6360+66G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 46/52 | chr12 | 109258430 | ||||||
| chr12:109258618
|
C | T | 1 | a0003c0005t0002g0134 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.6360+254C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 46/52 | chr12 | 109258618 | ||||||
| chr12:109258956
|
G | A | 2 | a0001c0038t0001g0029a0020c0052t0001g0210 | 2 | HG03492.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.6361-17G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 46/52 | chr12 | 109258956 | ||||||
| chr12:109259178
|
G | C | 1 | a0032c0059t0002g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.6496+70G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109259178 | ||||||
| chr12:109259180
|
G | A | 1 | a0032c0059t0002g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.6496+72G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109259180 | ||||||
| chr12:109259181
|
A | ATGTCCTA others(13): Show |
1 | a0032c0059t0002g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.6496+75_6496+76ins others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | INFO_REALIGN_3_PRIME | chr12 | 109259181 | |||||
| chr12:109259213
|
C | G | 6 | a0002c0028t0003g0160a0002c0028t0003g0179a0002c0028t0003g0228others(3): Show | 6 | HG00609.hp1 HG02015.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.6496+105C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109259213 | ||||||
| chr12:109259231
|
C | G | 1 | a0001c0003t0004g0074 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6496+123C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109259231 | ||||||
| chr12:109259380
|
C | T | 1 | a0002c0036t0006g0223 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.6496+272C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109259380 | ||||||
| chr12:109259390
|
A | G | 2 | a0001c0069t0002g0204a0001c0124t0012g0197 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.6496+282A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109259390 | ||||||
| chr12:109259563
|
C | CA | 22 | a0001c0003t0002g0094a0001c0004t0007g0019a0001c0010t0002g0261others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.6496+466dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | INFO_REALIGN_3_PRIME | chr12 | 109259563 | |||||
| chr12:109259577
|
AAAAAAC | A | 7 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.6496+475_6496+480d others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | INFO_REALIGN_3_PRIME | chr12 | 109259577 | |||||
| chr12:109259583
|
C | A | 2 | a0003c0001t0004g0266a0006c0113t0004g0031 | 2 | NA18983.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.6496+475C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109259583 | ||||||
| chr12:109259583
|
C | CA | 72 | a0001c0003t0002g0068a0001c0003t0002g0077a0001c0003t0002g0078others(69): Show | 72 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.6496+485dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | INFO_REALIGN_3_PRIME | chr12 | 109259583 | |||||
| chr12:109259593
|
A | T | 14 | a0002c0006t0005g0123a0002c0006t0005g0284a0002c0006t0005g0294others(11): Show | 14 | HG01081.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.6496+485A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109259593 | ||||||
| chr12:109259618
|
C | T | 1 | a0003c0001t0004g0266 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.6496+510C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109259618 | ||||||
| chr12:109259686
|
G | A | 1 | a0008c0015t0005g0057 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.6496+578G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109259686 | ||||||
| chr12:109259743
|
C | T | 7 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.6496+635C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109259743 | ||||||
| chr12:109259840
|
T | C | 1 | a0032c0059t0002g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.6497-640T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109259840 | ||||||
| chr12:109259991
|
A | G | 222 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.6497-489A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109259991 | ||||||
| chr12:109260358
|
C | T | 3 | a0002c0007t0003g0055a0002c0007t0022g0032a0010c0042t0003g0220 | 3 | HG01167.hp1 HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.6497-122C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | chr12 | 109260358 | ||||||
| chr12:109260761
|
T | A | 215 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.6674+104T>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109260761 | ||||||
| chr12:109260835
|
A | C | 2 | a0033c0063t0010g0117a0035c0076t0010g0267 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.6674+178A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109260835 | ||||||
| chr12:109260942
|
A | G | 3 | a0001c0002t0001g0126a0001c0023t0001g0089a0001c0108t0001g0010 | 3 | HG01123.hp2 HG02258.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.6674+285A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109260942 | ||||||
| chr12:109261125
|
T | G | 7 | a0001c0004t0007g0001a0001c0004t0007g0011a0001c0004t0007g0019others(4): Show | 8 | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.6674+468T>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261125 | ||||||
| chr12:109261149
|
A | C | 15 | a0007c0030t0004g0280a0007c0030t0004g0285a0007c0037t0004g0073others(12): Show | 15 | HG01168.hp2 HG01261.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.6674+492A>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261149 | ||||||
| chr12:109261163
|
A | G | 1 | a0001c0039t0004g0116 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6674+506A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261163 | ||||||
| chr12:109261196
|
C | A | 7 | a0001c0004t0007g0001a0001c0004t0007g0011a0001c0004t0007g0019others(4): Show | 8 | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.6674+539C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261196 | ||||||
| chr12:109261608
|
C | G | 1 | a0006c0031t0004g0002 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.6675-749C>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261608 | ||||||
| chr12:109261613
|
G | A | 8 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(5): Show | 8 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.6675-744G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261613 | ||||||
| chr12:109261642
|
G | C | 74 | a0001c0003t0002g0068a0001c0003t0002g0077a0001c0003t0002g0078others(71): Show | 74 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.6675-715G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261642 | ||||||
| chr12:109261658
|
G | A | 5 | a0011c0027t0004g0150a0011c0027t0004g0249a0011c0027t0013g0065others(2): Show | 5 | HG01168.hp2 HG01261.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.6675-699G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261658 | ||||||
| chr12:109261763
|
C | T | 1 | a0007c0057t0004g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6675-594C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261763 | ||||||
| chr12:109261764
|
G | A | 1 | a0001c0016t0011g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.6675-593G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261764 | ||||||
| chr12:109261781
|
G | T | 7 | a0001c0004t0007g0001a0001c0004t0007g0011a0001c0004t0007g0019others(4): Show | 8 | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.6675-576G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261781 | ||||||
| chr12:109261811
|
T | C | 237 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.6675-546T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261811 | ||||||
| chr12:109261869
|
T | TA | 8 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(5): Show | 8 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.6675-478dupA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | INFO_REALIGN_3_PRIME | chr12 | 109261869 | |||||
| chr12:109261880
|
C | A | 2 | a0017c0123t0015g0058a0026c0066t0015g0115 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.6675-477C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261880 | ||||||
| chr12:109261939
|
A | G | 5 | a0011c0027t0004g0150a0011c0027t0004g0249a0011c0027t0013g0065others(2): Show | 5 | HG01168.hp2 HG01261.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.6675-418A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261939 | ||||||
| chr12:109261941
|
A | G | 2 | a0001c0069t0002g0204a0001c0124t0012g0197 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.6675-416A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109261941 | ||||||
| chr12:109262070
|
G | A | 1 | a0001c0039t0004g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6675-287G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109262070 | ||||||
| chr12:109262101
|
G | A | 2 | a0001c0069t0002g0204a0001c0124t0012g0197 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.6675-256G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109262101 | ||||||
| chr12:109262285
|
C | T | 1 | a0008c0044t0003g0182 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.6675-72C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | chr12 | 109262285 | ||||||
| chr12:109262515
|
C | T | 1 | a0001c0060t0002g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6787+46C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109262515 | ||||||
| chr12:109262544
|
G | A | 1 | a0009c0096t0009g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6787+75G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109262544 | ||||||
| chr12:109262619
|
G | T | 1 | a0001c0002t0001g0191 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.6787+150G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109262619 | ||||||
| chr12:109262764
|
C | T | 7 | a0001c0011t0008g0018a0001c0013t0001g0153a0001c0087t0001g0236others(4): Show | 7 | HG00423.hp2 HG00438.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.6787+295C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109262764 | ||||||
| chr12:109262814
|
G | A | 7 | a0001c0004t0007g0001a0001c0004t0007g0011a0001c0004t0007g0019others(4): Show | 8 | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.6787+345G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109262814 | ||||||
| chr12:109262950
|
T | TATATATA others(10): Show |
1 | a0001c0034t0001g0212 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.6787+481_6787+482i others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109262950 | ||||||
| chr12:109262950
|
T | TTA | 5 | a0001c0098t0001g0286a0001c0124t0012g0197a0002c0020t0003g0232others(2): Show | 5 | HG01433.hp1 HG02698.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.6787+513_6787+514d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATA | 13 | a0001c0003t0002g0103a0001c0016t0011g0274a0001c0069t0002g0204others(10): Show | 13 | HG00323.hp1 HG01167.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.6787+511_6787+514d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATA | 10 | a0001c0002t0001g0098a0001c0004t0002g0054a0001c0062t0019g0288others(7): Show | 10 | HG01081.hp1 HG01081.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.6787+509_6787+514d others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATAT others(1): Show |
17 | a0001c0012t0002g0045a0001c0012t0002g0251a0001c0029t0002g0096others(14): Show | 17 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.6787+507_6787+514d others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATAT others(3): Show |
16 | a0001c0002t0001g0109a0001c0012t0002g0250a0001c0016t0009g0305others(13): Show | 16 | HG00642.hp1 HG00735.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.6787+505_6787+514d others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATAT others(5): Show |
19 | a0001c0002t0001g0282a0001c0010t0002g0021a0001c0012t0002g0259others(16): Show | 19 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.6787+503_6787+514d others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATAT others(7): Show |
16 | a0001c0002t0001g0283a0001c0003t0002g0077a0001c0011t0001g0056others(13): Show | 16 | HG00558.hp2 HG01515.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.6787+501_6787+514d others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATAT others(9): Show |
18 | a0001c0002t0001g0235a0001c0010t0009g0186a0001c0013t0001g0163others(15): Show | 18 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.6787+499_6787+514d others(18): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATAT others(11): Show |
19 | a0001c0002t0001g0085a0001c0002t0001g0191a0001c0010t0001g0188others(16): Show | 19 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.6787+497_6787+514d others(20): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATAT others(13): Show |
15 | a0001c0002t0001g0081a0001c0002t0001g0091a0001c0002t0001g0114others(12): Show | 15 | HG01070.hp1 HG01261.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.6787+495_6787+514d others(22): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATAT others(15): Show |
15 | a0001c0002t0001g0079a0001c0011t0001g0008a0001c0013t0001g0153others(12): Show | 15 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.6787+493_6787+514d others(24): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATAT others(17): Show |
3 | a0001c0002t0001g0035a0001c0050t0001g0278a0028c0100t0001g0070 | 3 | NA18980.hp1 NA19003.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.6787+491_6787+514d others(26): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATAT others(19): Show |
3 | a0003c0001t0008g0128a0004c0008t0001g0218a0004c0008t0008g0263 | 3 | NA18981.hp1 NA19011.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.6787+489_6787+514d others(28): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATAT others(21): Show |
6 | a0001c0002t0001g0241a0001c0002t0001g0242a0002c0021t0006g0239others(3): Show | 6 | HG01106.hp2 NA18955.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.6787+487_6787+514d others(30): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATAT others(23): Show |
2 | a0003c0001t0001g0138a0011c0027t0004g0150 | 2 | HG01106.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.6787+485_6787+514d others(32): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTATATAT others(25): Show |
2 | a0013c0033t0002g0185a0013c0033t0002g0189 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.6787+483_6787+514d others(34): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTTATATA others(4): Show |
1 | a0001c0003t0002g0078 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6787+482_6787+483i others(13): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTTTATAT others(1): Show |
13 | a0001c0003t0002g0097a0001c0003t0002g0101a0001c0003t0002g0102others(10): Show | 13 | HG00438.hp1 HG00597.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.6787+482_6787+483i others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTTTATAT others(3): Show |
10 | a0001c0003t0002g0094a0001c0003t0002g0112a0001c0003t0002g0244others(7): Show | 10 | HG00621.hp2 HG01070.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.6787+482_6787+483i others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTTTATAT others(5): Show |
6 | a0001c0012t0002g0262a0001c0018t0011g0046a0001c0018t0011g0047others(3): Show | 6 | HG00408.hp2 HG00423.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.6787+482_6787+483i others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTTTATAT others(7): Show |
5 | a0001c0003t0002g0099a0001c0018t0002g0049a0001c0045t0002g0234others(2): Show | 5 | HG01433.hp2 HG02145.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.6787+482_6787+483i others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTTTATAT others(9): Show |
4 | a0001c0003t0002g0104a0001c0010t0002g0261a0001c0046t0002g0067others(1): Show | 4 | HG03669.hp2 NA18959.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.6787+482_6787+483i others(18): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTTTATAT others(15): Show |
1 | a0003c0005t0002g0059 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.6787+482_6787+483i others(24): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTTTATAT others(19): Show |
1 | a0003c0005t0002g0060 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.6787+482_6787+483i others(28): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
T | TTTTATAT others(21): Show |
1 | a0001c0029t0002g0108 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6787+482_6787+483i others(30): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
TTA | T | 6 | a0001c0002t0008g0306a0007c0030t0004g0280a0007c0030t0004g0285others(3): Show | 6 | HG02145.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.6787+513_6787+514d others(4): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
TTATA | T | 9 | a0001c0002t0001g0126a0001c0022t0004g0004a0001c0022t0004g0005others(6): Show | 9 | HG01123.hp2 HG02258.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.6787+511_6787+514d others(6): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
TTATATAT others(1): Show |
T | 8 | a0001c0003t0002g0068a0001c0004t0007g0001a0001c0004t0007g0011others(5): Show | 9 | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.6787+507_6787+514d others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
TTATATAT others(3): Show |
T | 17 | a0002c0006t0005g0123a0002c0006t0005g0284a0002c0006t0005g0294others(14): Show | 17 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.6787+505_6787+514d others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
TTATATAT others(5): Show |
T | 17 | a0001c0003t0004g0074a0001c0003t0004g0300a0001c0004t0017g0003others(14): Show | 17 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.6787+503_6787+514d others(14): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262950
|
TTATATAT others(9): Show |
T | 2 | a0002c0007t0003g0037a0002c0007t0003g0041 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6787+499_6787+514d others(18): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262950 | |||||
| chr12:109262960
|
A | T | 1 | a0001c0003t0002g0068 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.6787+491A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109262960 | ||||||
| chr12:109262962
|
A | ATATATAT others(10): Show |
1 | a0003c0001t0001g0087 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.6787+494_6787+510d others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109262962 | |||||
| chr12:109262983
|
T | TATATATA others(4): Show |
1 | a0002c0021t0003g0252 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.6787+514_6787+515i others(13): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109262983 | ||||||
| chr12:109263217
|
C | A | 1 | a0006c0031t0004g0002 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.6787+748C>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109263217 | ||||||
| chr12:109263279
|
C | T | 1 | a0005c0056t0003g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6787+810C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109263279 | ||||||
| chr12:109263783
|
A | G | 2 | a0001c0002t0001g0098a0037c0072t0001g0217 | 2 | HG01081.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.6788-449A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109263783 | ||||||
| chr12:109263831
|
C | T | 6 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.6788-401C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109263831 | ||||||
| chr12:109263863
|
A | T | 1 | a0001c0003t0002g0094 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6788-369A>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109263863 | ||||||
| chr12:109264154
|
CA | C | 81 | a0001c0003t0002g0068a0001c0003t0002g0077a0001c0003t0002g0078others(78): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.6788-63delA | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | 109264154 | |||||
| chr12:109264215
|
T | C | 17 | a0001c0003t0004g0074a0001c0003t0004g0300a0001c0004t0017g0003others(14): Show | 17 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.6788-17T>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | chr12 | 109264215 | ||||||
| chr12:109264448
|
G | A | 1 | a0003c0001t0001g0064 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.6942+62G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 50/52 | chr12 | 109264448 | ||||||
| chr12:109264599
|
C | T | 25 | a0001c0003t0004g0074a0001c0003t0004g0300a0001c0004t0007g0001others(22): Show | 26 | HG01891.hp1 HG01891.hp2 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.6942+213C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 50/52 | chr12 | 109264599 | ||||||
| chr12:109264930
|
G | A | 14 | a0002c0006t0005g0123a0002c0006t0005g0284a0002c0006t0005g0294others(11): Show | 14 | HG01081.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.6943-180G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 50/52 | chr12 | 109264930 | ||||||
| chr12:109264967
|
C | T | 1 | a0001c0062t0019g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6943-143C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 50/52 | chr12 | 109264967 | ||||||
| chr12:109265287
|
C | T | 4 | a0007c0037t0004g0073a0007c0104t0004g0183a0015c0114t0004g0009others(1): Show | 4 | HG02559.hp1 HG03486.hp2 HG06807.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.7113+7C>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 51/52 | chr12 | 109265287 | ||||||
| chr12:109265335
|
A | G | 21 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(18): Show | 21 | HG01081.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.7114-54A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 51/52 | chr12 | 109265335 | ||||||
| chr12:109265349
|
G | C | 6 | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.7114-40G>C | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 51/52 | chr12 | 109265349 | ||||||
| chr12:109265622
|
G | A | 4 | a0002c0092t0010g0192a0033c0063t0010g0117a0035c0076t0010g0267others(1): Show | 4 | HG03098.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.7250+97G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 52/52 | chr12 | 109265622 | ||||||
| chr12:109265651
|
G | A | 92 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.7250+126G>A | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 52/52 | chr12 | 109265651 | ||||||
| chr12:109265832
|
A | G | 1 | a0001c0050t0001g0278 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.7250+307A>G | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 52/52 | chr12 | 109265832 | ||||||
| chr12:109265882
|
G | T | 3 | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0055t0001g0226 | 3 | HG02630.hp1 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.7251-354G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 52/52 | chr12 | 109265882 | ||||||
| chr12:109266147
|
G | T | 1 | a0001c0048t0004g0307 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.7251-89G>T | ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 52/52 | chr12 | 109266147 |