| geneid | 51144 |
|---|---|
| ensemblid | ENSG00000149084.13 |
| hgncid | 18646 |
| symbol | HSD17B12 |
| name | hydroxysteroid 17-beta dehydrogenase 12 |
| refseq_nuc | NM_016142.3 |
| refseq_prot | NP_057226.1 |
| ensembl_nuc | ENST00000278353.10 |
| ensembl_prot | ENSP00000278353.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 43680738 |
| end | 43856615 |
| strand | + |
| ver | v1.2 |
| region | chr11:43680738-43856615 |
| region5000 | chr11:43675738-43861615 |
| regionname0 | HSD17B12_chr11_43680738_43856615 |
| regionname5000 | HSD17B12_chr11_43675738_43861615 |
| 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 | 1/0 | 312 | 176 | 49 | 30 | 58 | 11 | 27 | 45 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0002 | 0/1 | 312 | 98 | 34 | 24 | 27 | 5 | 7 | 19 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0003 | 0/0 | 312 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0004 | 0/0 | 312 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0005 | 0/0 | 312 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| 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 | 1/0 | 939 | 151 | 45 | 20 | 58 | 8 | 19 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| c0002 | 0/1 | 939 | 98 | 34 | 24 | 27 | 5 | 7 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| c0003 | 0/0 | 939 | 24 | 3 | 10 | 0 | 3 | 8 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| c0004 | 0/0 | 939 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| c0005 | 0/0 | 939 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| c0006 | 0/0 | 939 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| c0007 | 0/0 | 939 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| 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 | 1/0 | 1458 | 152 | 45 | 27 | 46 | 9 | 24 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| t0002 | 0/1 | 1768 | 92 | 29 | 24 | 27 | 5 | 6 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| t0003 | 0/0 | 1458 | 26 | 6 | 3 | 12 | 2 | 3 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| t0004 | 0/0 | 1774 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| t0005 | 0/0 | 1768 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| t0006 | 0/0 | 1768 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| t0007 | 0/0 | 1768 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| t0008 | 0/0 | 1774 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| t0009 | 0/0 | 1774 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| t0010 | 0/0 | 1768 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| t0011 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| t0012 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| 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 | 2 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0278 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 939 | 151 | 45 | 20 | 58 | 8 | 19 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0001c0003 | 0/0 | 939 | 24 | 3 | 10 | 0 | 3 | 8 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0001c0007 | 0/0 | 939 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0002c0002 | 0/1 | 939 | 98 | 34 | 24 | 27 | 5 | 7 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0003c0004 | 0/0 | 939 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0004c0005 | 0/0 | 939 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0005c0006 | 0/0 | 939 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2396 | 133 | 40 | 20 | 46 | 7 | 19 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0001c0001t0003 | 0/0 | 2396 | 17 | 4 | 0 | 12 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0001c0001t0011 | 0/0 | 2396 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0001c0003t0001 | 0/0 | 2396 | 15 | 1 | 7 | 0 | 2 | 5 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0001c0003t0003 | 0/0 | 2396 | 9 | 2 | 3 | 0 | 1 | 3 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0001c0007t0001 | 0/0 | 2396 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0002c0002t0002 | 0/1 | 2706 | 90 | 29 | 22 | 27 | 5 | 6 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0002c0002t0004 | 0/0 | 2712 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0002c0002t0005 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0002c0002t0006 | 0/0 | 2706 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0002c0002t0007 | 0/0 | 2706 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0002c0002t0008 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0002c0002t0009 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0002c0002t0010 | 0/0 | 2706 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0003c0004t0001 | 0/0 | 2396 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0004c0005t0002 | 0/0 | 2706 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| a0005c0006t0012 | 0/0 | 2396 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | copy fasta | chr11 | 43675738 | 43861615 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0278 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0011g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0007t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0006g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0007g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0008g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0009g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0010g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0003c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0003c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0003c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0004c0005t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0004c0005t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0005c0006t0012g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | GBR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0273 | EUR | GBR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0188 | EUR | GBR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0022 | EUR | FIN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0177 | EUR | FIN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0163 | EUR | FIN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | CHS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | CHS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | CHS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00609 | hp2 | a0005 | c0006 | t0012 | g0020 | EAS | CHS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0139 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0237 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0026 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0274 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00735 | hp1 | a0002 | c0002 | t0006 | g0107 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0174 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0238 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0128 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01070 | hp2 | a0001 | c0003 | t0003 | g0250 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01071 | hp1 | a0001 | c0003 | t0003 | g0251 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0165 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01099 | hp2 | a0004 | c0005 | t0002 | g0011 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0239 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01106 | hp2 | a0004 | c0005 | t0002 | g0010 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01109 | hp2 | a0002 | c0002 | t0007 | g0146 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0189 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0226 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0132 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0064 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0181 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0190 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0166 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0159 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0167 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0240 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0057 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0140 | EUR | IBS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0147 | EUR | IBS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0155 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0255 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0055 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0101 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0236 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0065 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02004 | hp1 | a0001 | c0003 | t0003 | g0248 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | CDX | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | CDX | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0138 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02258 | hp1 | a0001 | c0007 | t0001 | g0232 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0056 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0253 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0109 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02451 | hp1 | a0002 | c0002 | t0004 | g0206 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0186 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0162 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0156 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0176 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02647 | hp2 | a0003 | c0004 | t0001 | g0244 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0039 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0157 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0153 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0233 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0178 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0276 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0182 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0241 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0134 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0133 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02896 | hp1 | a0001 | c0003 | t0003 | g0235 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0234 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02970 | hp1 | a0002 | c0002 | t0004 | g0275 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0142 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0202 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0145 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0171 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0172 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0263 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0270 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0154 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03239 | hp2 | a0001 | c0003 | t0003 | g0247 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0195 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03516 | hp2 | a0003 | c0004 | t0001 | g0231 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0277 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0252 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0135 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0243 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03654 | hp2 | a0001 | c0003 | t0003 | g0245 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0199 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03942 | hp2 | a0001 | c0003 | t0003 | g0246 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0168 | SAS | STU | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0242 | SAS | STU | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0151 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04199 | hp1 | a0002 | c0002 | t0010 | g0158 | SAS | STU | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0198 | SAS | STU | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | YRI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | CHB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | CHB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | YRI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18906 | hp2 | a0002 | c0002 | t0008 | g0002 | AFR | YRI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19030 | hp1 | a0002 | c0002 | t0005 | g0208 | AFR | LWK | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | LWK | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19043 | hp1 | a0002 | c0002 | t0009 | g0201 | AFR | LWK | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | LWK | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ASW | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0193 | AFR | ASW | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | TSI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0228 | EUR | TSI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20805 | hp1 | a0001 | c0003 | t0003 | g0249 | EUR | TSI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | TSI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0024 | SAS | GIH | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0141 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0194 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0144 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | USA | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0254 | AFR | USA | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0256 | AFR | USA | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | USA | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0173 | REF | REF | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0278 | REF | REF | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43680844
|
C | T | 1 | a0004 | 2 | HG01099.hp2 HG01106.hp2 |
missense_variant | MODERATE | c.17C>T | p.Pro6Leu | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/11 | 107/2396 | 17/939 | 6/312 | chr11 | 43680844 | ||
| chr11:43838378
|
A | G | 1 | a0003 | 3 | HG02647.hp2 HG03516.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.598A>G | p.Thr200Ala | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/11 | 688/2396 | 598/939 | 200/312 | chr11 | 43838378 | ||
| chr11:43855148
|
C | T | 2 | a0002a0004 | 100 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(97): Show |
missense_variant | MODERATE | c.839C>T | p.Ser280Leu | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 929/2396 | 839/939 | 280/312 | chr11 | 43855148 | ||
| chr11:43855221
|
C | G | 1 | a0005 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.912C>G | p.His304Gln | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 1002/2396 | 912/939 | 304/312 | chr11 | 43855221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43680980
|
A | G | 3 | a0001c0003a0001c0007a0003c0004 | 28 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
synonymous_variant | LOW | c.153A>G | p.Glu51Glu | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/11 | 243/2396 | 153/939 | 51/312 | chr11 | 43680980 | ||
| chr11:43854855
|
T | C | 1 | a0001c0007 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.825T>C | p.His275His | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 10/11 | 915/2396 | 825/939 | 275/312 | chr11 | 43854855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43855263
|
A | C | 4 | a0001c0001t0003a0001c0001t0011a0001c0003t0003others(1): Show | 28 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*15A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 15 | chr11 | 43855263 | |||||
| chr11:43855279
|
A | G | 4 | a0001c0001t0003a0001c0001t0011a0001c0003t0003others(1): Show | 28 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*31A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 31 | chr11 | 43855279 | |||||
| chr11:43855296
|
C | T | 1 | a0005c0006t0012 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*48C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 48 | chr11 | 43855296 | |||||
| chr11:43855513
|
A | G | 1 | a0001c0001t0011 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*265A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 265 | chr11 | 43855513 | |||||
| chr11:43855582
|
C | T | 1 | a0002c0002t0010 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*334C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 334 | chr11 | 43855582 | |||||
| chr11:43855654
|
CTTTTGT | C | 6 | a0002c0002t0002a0002c0002t0005a0002c0002t0006others(3): Show | 96 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*412_*417delTTTTTG | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 412 | INFO_REALIGN_3_PRIME | chr11 | 43855654 | ||||
| chr11:43855889
|
T | TCTCAGTT others(309): Show |
1 | a0002c0002t0005 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*650_*651insTTTTTT others(310): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 651 | INFO_REALIGN_3_PRIME | chr11 | 43855889 | ||||
| chr11:43855889
|
T | TCTCAGTT others(309): Show |
1 | a0002c0002t0006 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*650_*651insTTTTTT others(310): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 651 | INFO_REALIGN_3_PRIME | chr11 | 43855889 | ||||
| chr11:43855889
|
T | TCTCAGTT others(309): Show |
4 | a0002c0002t0002a0002c0002t0007a0002c0002t0010others(1): Show | 94 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*650_*651insTTTTTT others(310): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 651 | INFO_REALIGN_3_PRIME | chr11 | 43855889 | ||||
| chr11:43855889
|
T | TCTCAGTT others(309): Show |
1 | a0002c0002t0004 | 2 | HG02451.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*650_*651insTTTTTT others(310): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 651 | INFO_REALIGN_3_PRIME | chr11 | 43855889 | ||||
| chr11:43855889
|
T | TCTCAGTT others(309): Show |
1 | a0002c0002t0008 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*650_*651insTTTTTT others(310): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 651 | INFO_REALIGN_3_PRIME | chr11 | 43855889 | ||||
| chr11:43855889
|
T | TCTCAGTT others(309): Show |
1 | a0002c0002t0009 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*650_*651insTTTTTT others(310): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 651 | INFO_REALIGN_3_PRIME | chr11 | 43855889 | ||||
| chr11:43856384
|
C | A | 8 | a0002c0002t0002a0002c0002t0004a0002c0002t0005others(5): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1136C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 1136 | chr11 | 43856384 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43681031
|
G | A | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.160+44G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681031 | ||||||
| chr11:43681040
|
C | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+53C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681040 | ||||||
| chr11:43681065
|
G | C | 275 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.160+78G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681065 | ||||||
| chr11:43681164
|
A | T | 1 | a0002c0002t0004g0275 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.160+177A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681164 | ||||||
| chr11:43681294
|
A | G | 1 | a0001c0003t0001g0274 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.160+307A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681294 | ||||||
| chr11:43681333
|
C | T | 1 | a0001c0003t0001g0273 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.160+346C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681333 | ||||||
| chr11:43681409
|
G | T | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.160+422G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681409 | ||||||
| chr11:43681423
|
G | A | 2 | a0004c0005t0002g0010a0004c0005t0002g0011 | 2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.160+436G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681423 | ||||||
| chr11:43681437
|
T | C | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.160+450T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681437 | ||||||
| chr11:43681500
|
A | AATCGTAC others(6): Show |
1 | a0001c0001t0001g0271 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.160+515_160+527dup others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43681500 | |||||
| chr11:43681566
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 12 | HG01261.hp2 HG02257.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.160+579A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681566 | ||||||
| chr11:43681645
|
T | C | 12 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(9): Show | 12 | HG00280.hp1 HG00609.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.160+658T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681645 | ||||||
| chr11:43681646
|
G | A | 2 | a0001c0003t0001g0198a0001c0003t0001g0199 | 2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.160+659G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681646 | ||||||
| chr11:43681670
|
AT | A | 103 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(100): Show | 104 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.160+698delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43681670 | |||||
| chr11:43681685
|
T | C | 106 | a0001c0001t0001g0114a0001c0001t0001g0119a0001c0001t0001g0120others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.160+698T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681685 | ||||||
| chr11:43681824
|
TC | T | 22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(19): Show | 22 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.160+847delC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43681824 | |||||
| chr11:43681834
|
C | CT | 23 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0001g0210others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.160+857dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43681834 | |||||
| chr11:43681834
|
CT | C | 29 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(26): Show | 29 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.160+857delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43681834 | |||||
| chr11:43681835
|
T | C | 3 | a0001c0001t0001g0230a0001c0003t0001g0198a0003c0004t0001g0231 | 3 | HG02922.hp1 HG03516.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.160+848T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681835 | ||||||
| chr11:43681895
|
C | T | 1 | a0002c0002t0002g0109 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.160+908C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681895 | ||||||
| chr11:43681967
|
T | G | 2 | a0001c0001t0001g0114a0002c0002t0002g0115 | 2 | NA19068.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.160+980T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681967 | ||||||
| chr11:43682030
|
T | C | 3 | a0002c0002t0002g0116a0002c0002t0002g0117a0002c0002t0002g0118 | 3 | HG00408.hp2 HG02135.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.160+1043T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682030 | ||||||
| chr11:43682434
|
C | T | 1 | a0003c0004t0001g0252 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.160+1447C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682434 | ||||||
| chr11:43682490
|
C | G | 111 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.160+1503C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682490 | ||||||
| chr11:43682496
|
C | T | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1509C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682496 | ||||||
| chr11:43682497
|
A | G | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1510A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682497 | ||||||
| chr11:43682498
|
T | C | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1511T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682498 | ||||||
| chr11:43682508
|
C | G | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1521C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682508 | ||||||
| chr11:43682508
|
CTCCA | C | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.160+1526_160+1529d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43682508 | |||||
| chr11:43682512
|
A | G | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1525A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682512 | ||||||
| chr11:43682516
|
A | G | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1529A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682516 | ||||||
| chr11:43682517
|
G | A | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1530G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682517 | ||||||
| chr11:43682524
|
T | C | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1537T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682524 | ||||||
| chr11:43682540
|
A | G | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1553A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682540 | ||||||
| chr11:43682544
|
C | CAAAAAAA others(12): Show |
1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1561_160+1579d others(21): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43682544 | |||||
| chr11:43682544
|
CA | C | 42 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0119others(39): Show | 42 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.160+1579delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43682544 | |||||
| chr11:43682544
|
CAA | C | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 101 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.160+1578_160+1579d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43682544 | |||||
| chr11:43682544
|
CAAA | C | 121 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(118): Show | 121 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.160+1577_160+1579d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43682544 | |||||
| chr11:43682560
|
A | C | 111 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.160+1573A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682560 | ||||||
| chr11:43682593
|
A | G | 7 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+1606A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682593 | ||||||
| chr11:43682790
|
C | CT | 107 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(104): Show | 108 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.160+1814dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43682790 | |||||
| chr11:43682965
|
T | G | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 116 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.160+1978T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682965 | ||||||
| chr11:43682972
|
T | A | 227 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.160+1985T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682972 | ||||||
| chr11:43683085
|
C | A | 23 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0001g0210others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.160+2098C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43683085 | ||||||
| chr11:43683096
|
T | G | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 116 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.160+2109T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43683096 | ||||||
| chr11:43683097
|
T | G | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160+2110T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43683097 | ||||||
| chr11:43683104
|
G | GT | 17 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0209others(14): Show | 17 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.160+2132dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43683104 | |||||
| chr11:43683104
|
G | T | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 129 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.160+2117G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43683104 | ||||||
| chr11:43683107
|
T | G | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 116 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.160+2120T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43683107 | ||||||
| chr11:43683962
|
G | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.160+2975G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43683962 | ||||||
| chr11:43684041
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.160+3054T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43684041 | ||||||
| chr11:43684073
|
C | G | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.160+3086C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43684073 | ||||||
| chr11:43684118
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.160+3131G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43684118 | ||||||
| chr11:43684727
|
G | A | 1 | a0002c0002t0002g0128 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.160+3740G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43684727 | ||||||
| chr11:43684773
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG01168.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.160+3786G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43684773 | ||||||
| chr11:43684784
|
A | G | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.160+3797A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43684784 | ||||||
| chr11:43685119
|
C | G | 1 | a0002c0002t0002g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.160+4132C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685119 | ||||||
| chr11:43685284
|
T | TACTTTGC others(14): Show |
10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+4297_160+4298i others(23): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685284 | ||||||
| chr11:43685286
|
C | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+4299C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685286 | ||||||
| chr11:43685286
|
C | CTTTGCTT others(14): Show |
240 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.160+4299_160+4300i others(23): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685286 | ||||||
| chr11:43685382
|
G | T | 3 | a0001c0001t0001g0264a0001c0001t0001g0265a0002c0002t0002g0263 | 3 | HG02258.hp2 HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.160+4395G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685382 | ||||||
| chr11:43685390
|
A | G | 1 | a0002c0002t0005g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.160+4403A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685390 | ||||||
| chr11:43685582
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.160+4595C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685582 | ||||||
| chr11:43685814
|
C | T | 77 | a0001c0001t0001g0152a0001c0001t0001g0187a0001c0001t0001g0266others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.160+4827C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685814 | ||||||
| chr11:43686010
|
T | A | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.160+5023T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686010 | ||||||
| chr11:43686093
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.160+5106G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686093 | ||||||
| chr11:43686342
|
A | G | 2 | a0001c0003t0003g0234a0001c0003t0003g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.160+5355A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686342 | ||||||
| chr11:43686351
|
G | A | 1 | a0001c0003t0003g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.160+5364G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686351 | ||||||
| chr11:43686361
|
A | G | 2 | a0002c0002t0002g0191a0002c0002t0002g0192 | 2 | NA18982.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.160+5374A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686361 | ||||||
| chr11:43686476
|
T | C | 278 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.160+5489T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686476 | ||||||
| chr11:43686525
|
C | T | 1 | a0002c0002t0002g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+5538C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686525 | ||||||
| chr11:43686531
|
T | C | 278 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.160+5544T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686531 | ||||||
| chr11:43686551
|
T | C | 278 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.160+5564T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686551 | ||||||
| chr11:43686579
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.160+5592C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686579 | ||||||
| chr11:43686581
|
A | G | 3 | a0002c0002t0002g0188a0002c0002t0002g0189a0002c0002t0002g0190 | 3 | HG00140.hp2 HG01167.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.160+5594A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686581 | ||||||
| chr11:43686595
|
G | GT | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.160+5625dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43686595 | |||||
| chr11:43686595
|
G | GTT | 8 | a0001c0001t0001g0063a0001c0001t0001g0104a0001c0001t0001g0187others(5): Show | 8 | HG01099.hp2 HG01106.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+5624_160+5625d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43686595 | |||||
| chr11:43686595
|
GT | G | 32 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0001g0210others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.160+5625delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43686595 | |||||
| chr11:43686859
|
G | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+5872G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686859 | ||||||
| chr11:43687001
|
T | A | 1 | a0001c0001t0001g0203 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.160+6014T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687001 | ||||||
| chr11:43687007
|
CTTTCAG | C | 91 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(88): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+6027_160+6032d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43687007 | |||||
| chr11:43687030
|
C | CAGA | 228 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.160+6044_160+6046d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43687030 | |||||
| chr11:43687152
|
C | T | 228 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.160+6165C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687152 | ||||||
| chr11:43687175
|
C | T | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.160+6188C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687175 | ||||||
| chr11:43687202
|
A | G | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.160+6215A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687202 | ||||||
| chr11:43687436
|
A | G | 250 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.160+6449A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687436 | ||||||
| chr11:43687836
|
C | T | 91 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(88): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+6849C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687836 | ||||||
| chr11:43687854
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+6867C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687854 | ||||||
| chr11:43687879
|
C | G | 250 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.160+6892C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687879 | ||||||
| chr11:43687925
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.160+6938C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687925 | ||||||
| chr11:43687937
|
C | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(30): Show | 33 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.160+6950C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687937 | ||||||
| chr11:43687986
|
C | T | 1 | a0002c0002t0002g0185 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.160+6999C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687986 | ||||||
| chr11:43688176
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.160+7189C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688176 | ||||||
| chr11:43688211
|
C | CA | 22 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0003t0001g0198others(19): Show | 22 | HG00639.hp2 HG01069.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.160+7238dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43688211 | |||||
| chr11:43688261
|
T | C | 1 | a0001c0001t0001g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.160+7274T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688261 | ||||||
| chr11:43688328
|
A | G | 1 | a0002c0002t0002g0184 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.160+7341A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688328 | ||||||
| chr11:43688367
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+7380C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688367 | ||||||
| chr11:43688384
|
G | A | 1 | a0001c0003t0001g0228 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.160+7397G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688384 | ||||||
| chr11:43688415
|
G | T | 228 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.160+7428G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688415 | ||||||
| chr11:43688519
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.160+7532A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688519 | ||||||
| chr11:43688527
|
C | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+7540C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688527 | ||||||
| chr11:43688674
|
C | T | 1 | a0001c0003t0001g0242 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.160+7687C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688674 | ||||||
| chr11:43688712
|
T | C | 1 | a0002c0002t0002g0138 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.160+7725T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688712 | ||||||
| chr11:43689057
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.160+8070G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43689057 | ||||||
| chr11:43689213
|
A | G | 2 | a0002c0002t0002g0127a0002c0002t0002g0183 | 2 | NA18964.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.160+8226A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43689213 | ||||||
| chr11:43689844
|
C | T | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.160+8857C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43689844 | ||||||
| chr11:43689912
|
C | G | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+8925C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43689912 | ||||||
| chr11:43689919
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG03453.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.160+8932C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43689919 | ||||||
| chr11:43690189
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0207 | 3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.160+9202C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690189 | ||||||
| chr11:43690361
|
C | CAT | 4 | a0002c0002t0002g0143a0002c0002t0002g0185a0002c0002t0002g0188others(1): Show | 4 | HG00140.hp2 HG02723.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+9417_160+9418d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | |||||
| chr11:43690361
|
C | CATAT | 3 | a0002c0002t0002g0139a0002c0002t0002g0140a0002c0002t0002g0141 | 3 | HG00639.hp1 HG01123.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.160+9415_160+9418d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | |||||
| chr11:43690361
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+9374C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690361 | ||||||
| chr11:43690361
|
CAT | C | 16 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0059others(13): Show | 16 | HG00323.hp1 HG01175.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+9417_160+9418d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | |||||
| chr11:43690361
|
CATAT | C | 17 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0036others(14): Show | 17 | HG00738.hp2 HG01168.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.160+9415_160+9418d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | |||||
| chr11:43690361
|
CATATATA others(1): Show |
C | 6 | a0001c0001t0001g0200a0001c0001t0001g0227a0001c0001t0001g0264others(3): Show | 6 | HG00140.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+9411_160+9418d others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | |||||
| chr11:43690361
|
CATATATA others(3): Show |
C | 3 | a0001c0001t0001g0218a0001c0001t0001g0222a0001c0003t0001g0226 | 3 | HG01167.hp2 HG01168.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.160+9409_160+9418d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | |||||
| chr11:43690361
|
CATATATA others(7): Show |
C | 2 | a0001c0001t0001g0114a0002c0002t0002g0115 | 2 | NA19068.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.160+9405_160+9418d others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | |||||
| chr11:43690361
|
CATATATA others(9): Show |
C | 3 | a0002c0002t0002g0171a0002c0002t0002g0176a0002c0002t0002g0178 | 3 | HG02647.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.160+9403_160+9418d others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | |||||
| chr11:43690361
|
CATATATA others(19): Show |
C | 2 | a0002c0002t0002g0179a0002c0002t0002g0181 | 2 | HG01258.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.160+9393_160+9418d others(28): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | |||||
| chr11:43690361
|
CATATATA others(23): Show |
C | 1 | a0002c0002t0002g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.160+9389_160+9418d others(32): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | |||||
| chr11:43690365
|
T | C | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+9378T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690365 | ||||||
| chr11:43690379
|
TATATATA others(2): Show |
T | 12 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(9): Show | 12 | HG01928.hp2 HG02523.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.160+9393_160+9401d others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690379 | ||||||
| chr11:43690379
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+9393_160+9403d others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690379 | ||||||
| chr11:43690379
|
TATATATA others(18): Show |
T | 1 | a0002c0002t0002g0180 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.160+9393_160+9417d others(27): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690379 | ||||||
| chr11:43690381
|
TATATATA others(2): Show |
T | 4 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(1): Show | 4 | HG00099.hp2 HG01261.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+9395_160+9403d others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690381 | ||||||
| chr11:43690383
|
TATATATA others(14): Show |
T | 1 | a0002c0002t0002g0256 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.160+9397_160+9417d others(23): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690383 | ||||||
| chr11:43690384
|
ATATATAT others(14): Show |
A | 3 | a0002c0002t0002g0253a0002c0002t0002g0254a0002c0002t0002g0255 | 3 | HG01891.hp1 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.160+9399_160+9419d others(23): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690384 | |||||
| chr11:43690385
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG01975.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.160+9398T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690385 | ||||||
| chr11:43690386
|
A | T | 1 | a0002c0002t0002g0177 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.160+9399A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690386 | ||||||
| chr11:43690386
|
ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.160+9401_160+9419d others(21): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690386 | |||||
| chr11:43690387
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0073 | 2 | HG01175.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.160+9400T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690387 | ||||||
| chr11:43690387
|
TA | T | 3 | a0001c0001t0001g0009a0002c0002t0002g0191a0002c0002t0002g0192 | 3 | HG02257.hp1 NA18982.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.160+9401delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690387 | ||||||
| chr11:43690387
|
TATA | T | 15 | a0001c0001t0001g0027a0001c0001t0001g0058a0001c0001t0001g0070others(12): Show | 16 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.160+9401_160+9403d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690387 | ||||||
| chr11:43690387
|
TATATATA others(8): Show |
T | 1 | a0002c0002t0002g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.160+9401_160+9415d others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690387 | ||||||
| chr11:43690387
|
TATATATA others(10): Show |
T | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.160+9401_160+9417d others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690387 | ||||||
| chr11:43690388
|
A | AT | 10 | a0001c0001t0001g0130a0001c0003t0001g0233a0001c0003t0001g0240others(7): Show | 10 | HG01361.hp2 HG02717.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+9402dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690388 | |||||
| chr11:43690388
|
A | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0200a0001c0003t0001g0273others(9): Show | 12 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(9): Show |
intron_variant | MODIFIER | c.160+9401A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690388 | ||||||
| chr11:43690389
|
TA | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0007t0001g0232 | 3 | HG02258.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.160+9403delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690389 | ||||||
| chr11:43690389
|
TATA | T | 23 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0034others(20): Show | 23 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.160+9403_160+9405d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690389 | ||||||
| chr11:43690390
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0126 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.160+9404_160+9405i others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690390 | |||||
| chr11:43690390
|
A | T | 60 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0053others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.160+9403A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690390 | ||||||
| chr11:43690391
|
TA | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0083others(1): Show | 4 | HG00735.hp2 HG02300.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+9405delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690391 | ||||||
| chr11:43690391
|
TATA | T | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0063others(5): Show | 8 | HG01192.hp1 HG02083.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+9405_160+9407d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690391 | ||||||
| chr11:43690392
|
A | ATT | 3 | a0001c0003t0001g0243a0001c0003t0003g0234a0001c0003t0003g0235 | 3 | HG02896.hp1 HG02897.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.160+9406_160+9407i others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690392 | |||||
| chr11:43690392
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0267 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.160+9406_160+9407i others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690392 | |||||
| chr11:43690392
|
A | T | 98 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(95): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.160+9405A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690392 | ||||||
| chr11:43690394
|
A | T | 139 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0025others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.160+9407A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690394 | ||||||
| chr11:43690396
|
A | ATTTTTTT others(4): Show |
1 | a0005c0006t0012g0020 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.160+9410_160+9411i others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690396 | |||||
| chr11:43690396
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0003g0021 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.160+9410_160+9411i others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690396 | |||||
| chr11:43690396
|
A | T | 156 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0025others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.160+9409A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690396 | ||||||
| chr11:43690398
|
A | ATTTTTTT | 4 | a0001c0003t0003g0246a0001c0003t0003g0249a0001c0003t0003g0250others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+9412_160+9413i others(9): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690398 | |||||
| chr11:43690398
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.160+9412_160+9413i others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690398 | |||||
| chr11:43690398
|
A | ATTTTTTT others(5): Show |
5 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(2): Show | 5 | NA18747.hp1 NA18945.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+9412_160+9413i others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690398 | |||||
| chr11:43690398
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0003g0066 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.160+9412_160+9413i others(15): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690398 | |||||
| chr11:43690398
|
A | T | 169 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0025others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.160+9411A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690398 | ||||||
| chr11:43690400
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.160+9414_160+9415i others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690400 | |||||
| chr11:43690400
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0003g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160+9414_160+9415i others(15): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690400 | |||||
| chr11:43690400
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0003g0015 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.160+9414_160+9415i others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690400 | |||||
| chr11:43690400
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.160+9414_160+9415i others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690400 | |||||
| chr11:43690400
|
A | ATTTTTTT others(11): Show |
4 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG01109.hp1 HG01496.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+9414_160+9415i others(20): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690400 | |||||
| chr11:43690400
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0259 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.160+9414_160+9415i others(24): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690400 | |||||
| chr11:43690400
|
A | T | 184 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.160+9413A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690400 | ||||||
| chr11:43690402
|
A | ATTTTTTT others(5): Show |
1 | a0002c0002t0004g0275 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.160+9416_160+9417i others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690402 | |||||
| chr11:43690402
|
A | ATTTTTTT others(8): Show |
1 | a0002c0002t0004g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.160+9416_160+9417i others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690402 | |||||
| chr11:43690402
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0003g0014a0002c0002t0002g0162 | 2 | HG02622.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.160+9416_160+9417i others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690402 | |||||
| chr11:43690402
|
A | ATTTTTTT others(13): Show |
1 | a0001c0001t0001g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.160+9416_160+9417i others(22): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690402 | |||||
| chr11:43690402
|
A | T | 200 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.160+9415A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690402 | ||||||
| chr11:43690404
|
A | ATATATAT others(18): Show |
1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(27): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | ATATATAT others(3): Show |
1 | a0002c0002t0006g0107 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | ATATATTT others(11): Show |
1 | a0002c0002t0002g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(20): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | ATATATTT others(16): Show |
1 | a0002c0002t0002g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(25): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | ATATATTT others(25): Show |
1 | a0001c0001t0001g0266 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(34): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | ATATTTTT others(8): Show |
1 | a0001c0001t0003g0012 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | ATATTTTT others(9): Show |
1 | a0001c0001t0001g0262 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.160+9418_160+9419i others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | ATATTTTT others(10): Show |
1 | a0002c0002t0002g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | ATATTTTT others(11): Show |
2 | a0002c0002t0002g0145a0002c0002t0007g0146 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.160+9418_160+9419i others(20): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | ATATTTTT others(16): Show |
1 | a0001c0001t0001g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.160+9418_160+9419i others(25): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | ATTTTTTT others(8): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0258 | 2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160+9420_160+9434d others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | ATTTTTTT others(9): Show |
5 | a0001c0001t0001g0152a0001c0001t0001g0272a0002c0002t0002g0153others(2): Show | 5 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+9419_160+9434d others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | ATTTTTTT others(10): Show |
3 | a0001c0001t0001g0271a0002c0002t0002g0138a0002c0002t0002g0156 | 3 | HG02257.hp2 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.160+9418_160+9434d others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0003g0013 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.160+9434_160+9435i others(20): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | |||||
| chr11:43690404
|
A | T | 219 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.160+9417A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690404 | ||||||
| chr11:43690406
|
T | A | 3 | a0002c0002t0002g0131a0002c0002t0002g0136a0002c0002t0002g0137 | 3 | NA18943.hp2 NA18952.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.160+9419T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690406 | ||||||
| chr11:43690840
|
T | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.160+9853T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690840 | ||||||
| chr11:43690967
|
T | C | 1 | a0002c0002t0002g0168 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.160+9980T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690967 | ||||||
| chr11:43691144
|
A | C | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.160+10157A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43691144 | ||||||
| chr11:43691447
|
C | G | 1 | a0001c0001t0003g0022 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.160+10460C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43691447 | ||||||
| chr11:43691556
|
C | T | 22 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.160+10569C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43691556 | ||||||
| chr11:43691586
|
C | A | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+10599C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43691586 | ||||||
| chr11:43691637
|
C | A | 1 | a0001c0001t0001g0069 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.160+10650C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43691637 | ||||||
| chr11:43691689
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.160+10702A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43691689 | ||||||
| chr11:43692080
|
T | C | 5 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(2): Show | 5 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+11093T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692080 | ||||||
| chr11:43692293
|
C | T | 91 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(88): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+11306C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692293 | ||||||
| chr11:43692439
|
G | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.160+11452G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692439 | ||||||
| chr11:43692456
|
A | T | 13 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(10): Show | 13 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+11469A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692456 | ||||||
| chr11:43692853
|
A | AG | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+11866_160+1186 others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692853 | ||||||
| chr11:43692854
|
T | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+11867T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692854 | ||||||
| chr11:43692951
|
T | G | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+11964T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692951 | ||||||
| chr11:43693120
|
G | A | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+12133G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43693120 | ||||||
| chr11:43693218
|
T | C | 91 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(88): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+12231T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43693218 | ||||||
| chr11:43693299
|
A | T | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+12312A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43693299 | ||||||
| chr11:43693502
|
G | C | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.160+12515G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43693502 | ||||||
| chr11:43693517
|
T | C | 16 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0003t0001g0198others(13): Show | 16 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+12530T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43693517 | ||||||
| chr11:43693622
|
C | T | 1 | a0001c0001t0003g0019 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.160+12635C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43693622 | ||||||
| chr11:43694721
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.160+13734T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43694721 | ||||||
| chr11:43694813
|
G | GA | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.160+13834dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43694813 | |||||
| chr11:43694923
|
C | T | 268 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.160+13936C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43694923 | ||||||
| chr11:43695305
|
G | A | 9 | a0002c0002t0002g0001a0002c0002t0002g0026a0002c0002t0002g0055others(6): Show | 10 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.160+14318G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695305 | ||||||
| chr11:43695397
|
G | A | 3 | a0002c0002t0002g0188a0002c0002t0002g0189a0002c0002t0002g0190 | 3 | HG00140.hp2 HG01167.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.160+14410G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695397 | ||||||
| chr11:43695549
|
G | A | 3 | a0002c0002t0002g0116a0002c0002t0002g0117a0002c0002t0002g0118 | 3 | HG00408.hp2 HG02135.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.160+14562G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695549 | ||||||
| chr11:43695586
|
A | T | 1 | a0002c0002t0002g0057 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.160+14599A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695586 | ||||||
| chr11:43695601
|
A | G | 2 | a0002c0002t0002g0179a0002c0002t0002g0180 | 2 | NA18949.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.160+14614A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695601 | ||||||
| chr11:43695671
|
G | GTCT | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 95 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.160+14704_160+1470 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43695671 | |||||
| chr11:43695671
|
G | GTCTTCT | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0271others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+14701_160+1470 others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43695671 | |||||
| chr11:43695691
|
C | CTTG | 16 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0003t0001g0198others(13): Show | 16 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+14706_160+1470 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43695691 | |||||
| chr11:43695725
|
A | G | 33 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(30): Show | 33 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.160+14738A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695725 | ||||||
| chr11:43695945
|
G | A | 5 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(2): Show | 5 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+14958G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695945 | ||||||
| chr11:43695978
|
G | A | 91 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(88): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+14991G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695978 | ||||||
| chr11:43696009
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.160+15022C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696009 | ||||||
| chr11:43696154
|
C | T | 1 | a0003c0004t0001g0252 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.160+15167C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696154 | ||||||
| chr11:43696831
|
C | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0207 | 3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.160+15844C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696831 | ||||||
| chr11:43696893
|
C | T | 77 | a0001c0001t0001g0152a0001c0001t0001g0187a0001c0001t0001g0266others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.160+15906C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696893 | ||||||
| chr11:43696937
|
C | T | 1 | a0001c0003t0001g0228 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.160+15950C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696937 | ||||||
| chr11:43696955
|
G | T | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+15968G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696955 | ||||||
| chr11:43696964
|
G | A | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+15977G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696964 | ||||||
| chr11:43697115
|
G | A | 1 | a0002c0002t0002g0139 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.160+16128G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43697115 | ||||||
| chr11:43697551
|
C | T | 77 | a0001c0001t0001g0152a0001c0001t0001g0187a0001c0001t0001g0266others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.160+16564C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43697551 | ||||||
| chr11:43697558
|
A | T | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+16571A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43697558 | ||||||
| chr11:43697708
|
A | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0207 | 3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.160+16721A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43697708 | ||||||
| chr11:43698119
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+17132G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698119 | ||||||
| chr11:43698226
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.160+17239A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698226 | ||||||
| chr11:43698300
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+17313C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698300 | ||||||
| chr11:43698448
|
A | G | 3 | a0002c0002t0002g0131a0002c0002t0002g0136a0002c0002t0002g0137 | 3 | NA18943.hp2 NA18952.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.160+17461A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698448 | ||||||
| chr11:43698737
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.160+17750T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698737 | ||||||
| chr11:43698769
|
T | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG01168.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.160+17782T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698769 | ||||||
| chr11:43698800
|
G | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+17813G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698800 | ||||||
| chr11:43698823
|
A | C | 8 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(5): Show | 8 | HG02559.hp2 HG02572.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+17836A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698823 | ||||||
| chr11:43698882
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.160+17895C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698882 | ||||||
| chr11:43698883
|
C | T | 3 | a0002c0002t0002g0161a0002c0002t0002g0164a0002c0002t0002g0184 | 3 | HG02080.hp2 HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.160+17896C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698883 | ||||||
| chr11:43699098
|
G | T | 3 | a0002c0002t0002g0133a0002c0002t0002g0134a0002c0002t0002g0135 | 3 | HG02818.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.160+18111G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43699098 | ||||||
| chr11:43699216
|
A | T | 1 | a0001c0001t0001g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.160+18229A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43699216 | ||||||
| chr11:43699307
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0126 | 3 | HG01884.hp2 HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+18320A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43699307 | ||||||
| chr11:43699648
|
G | C | 1 | a0001c0001t0001g0219 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.160+18661G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43699648 | ||||||
| chr11:43699950
|
T | C | 135 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.160+18963T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43699950 | ||||||
| chr11:43699999
|
A | G | 2 | a0001c0003t0001g0226a0001c0003t0001g0273 | 2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.160+19012A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43699999 | ||||||
| chr11:43700122
|
C | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.160+19135C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700122 | ||||||
| chr11:43700288
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.160+19301G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700288 | ||||||
| chr11:43700327
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+19340G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700327 | ||||||
| chr11:43700341
|
C | T | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+19354C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700341 | ||||||
| chr11:43700392
|
C | T | 12 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(9): Show | 12 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.160+19405C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700392 | ||||||
| chr11:43700503
|
G | C | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.160+19516G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700503 | ||||||
| chr11:43700579
|
C | G | 91 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(88): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+19592C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700579 | ||||||
| chr11:43700631
|
C | T | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.160+19644C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700631 | ||||||
| chr11:43700663
|
A | T | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.160+19676A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700663 | ||||||
| chr11:43700739
|
C | T | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.160+19752C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700739 | ||||||
| chr11:43700756
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.160+19769T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700756 | ||||||
| chr11:43700851
|
A | G | 9 | a0001c0001t0001g0200a0001c0001t0001g0210a0001c0001t0001g0211others(6): Show | 9 | HG01928.hp2 HG02523.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+19864A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700851 | ||||||
| chr11:43700892
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0126 | 3 | HG01884.hp2 HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+19905T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700892 | ||||||
| chr11:43700941
|
C | T | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.160+19954C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700941 | ||||||
| chr11:43701355
|
C | T | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.160+20368C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701355 | ||||||
| chr11:43701366
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0126 | 3 | HG01884.hp2 HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+20379T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701366 | ||||||
| chr11:43701384
|
G | T | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.160+20397G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701384 | ||||||
| chr11:43701463
|
T | C | 1 | a0001c0001t0003g0279 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.160+20476T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701463 | ||||||
| chr11:43701660
|
G | T | 2 | a0002c0002t0002g0193a0002c0002t0002g0195 | 2 | HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.160+20673G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701660 | ||||||
| chr11:43701665
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.160+20678T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701665 | ||||||
| chr11:43701717
|
T | C | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+20730T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701717 | ||||||
| chr11:43701867
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.160+20880A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701867 | ||||||
| chr11:43702082
|
A | G | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+21095A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702082 | ||||||
| chr11:43702342
|
G | C | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.160+21355G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702342 | ||||||
| chr11:43702440
|
G | A | 228 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.160+21453G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702440 | ||||||
| chr11:43702510
|
G | A | 228 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.160+21523G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702510 | ||||||
| chr11:43702590
|
A | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+21603A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702590 | ||||||
| chr11:43702618
|
G | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.160+21631G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702618 | ||||||
| chr11:43702713
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.160+21726A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702713 | ||||||
| chr11:43702916
|
C | T | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.160+21929C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702916 | ||||||
| chr11:43702998
|
A | G | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+22011A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702998 | ||||||
| chr11:43703263
|
T | C | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.160+22276T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703263 | ||||||
| chr11:43703267
|
T | G | 1 | a0001c0003t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160+22280T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703267 | ||||||
| chr11:43703296
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.160+22309G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703296 | ||||||
| chr11:43703330
|
G | A | 1 | a0002c0002t0002g0116 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.160+22343G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703330 | ||||||
| chr11:43703430
|
G | A | 13 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(10): Show | 13 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+22443G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703430 | ||||||
| chr11:43703437
|
G | A | 1 | a0002c0002t0005g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.160+22450G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703437 | ||||||
| chr11:43703484
|
G | A | 17 | a0002c0002t0002g0128a0002c0002t0002g0140a0002c0002t0002g0147others(14): Show | 17 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.160+22497G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703484 | ||||||
| chr11:43703549
|
G | C | 5 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(2): Show | 5 | NA18966.hp2 NA18971.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+22562G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703549 | ||||||
| chr11:43703816
|
G | T | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.160+22829G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703816 | ||||||
| chr11:43703975
|
G | A | 4 | a0002c0002t0002g0131a0002c0002t0002g0136a0002c0002t0002g0137others(1): Show | 4 | NA18943.hp2 NA18952.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+22988G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703975 | ||||||
| chr11:43704069
|
C | T | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.160+23082C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43704069 | ||||||
| chr11:43704209
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+23222G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43704209 | ||||||
| chr11:43704661
|
G | A | 22 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.160+23674G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43704661 | ||||||
| chr11:43704908
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.160+23921C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43704908 | ||||||
| chr11:43705013
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.160+24026G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705013 | ||||||
| chr11:43705089
|
A | G | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+24102A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705089 | ||||||
| chr11:43705315
|
T | C | 5 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(2): Show | 5 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+24328T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705315 | ||||||
| chr11:43705568
|
T | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0069 | 2 | NA18945.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.160+24581T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705568 | ||||||
| chr11:43705751
|
CCT | C | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(95): Show | 98 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.160+24770_160+2477 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43705751 | |||||
| chr11:43705753
|
TCTCTC | T | 7 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0271others(4): Show | 7 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+24771_160+2477 others(9): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43705753 | |||||
| chr11:43705756
|
CTCCT | C | 9 | a0001c0003t0001g0241a0001c0003t0003g0235a0002c0002t0002g0128others(6): Show | 9 | HG00323.hp1 HG00609.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+24770_160+2477 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705756 | ||||||
| chr11:43705759
|
C | T | 1 | a0002c0002t0002g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.160+24772C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705759 | ||||||
| chr11:43705760
|
TC | T | 86 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.160+24774delC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705760 | ||||||
| chr11:43705761
|
C | T | 13 | a0001c0001t0001g0130a0001c0001t0001g0187a0002c0002t0002g0108others(10): Show | 13 | HG00423.hp1 HG01175.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.160+24774C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705761 | ||||||
| chr11:43705761
|
CT | C | 21 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 21 | HG00099.hp2 HG01167.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.160+24799delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43705761 | |||||
| chr11:43705761
|
CTT | C | 23 | a0001c0001t0001g0058a0001c0001t0001g0084a0001c0001t0001g0110others(20): Show | 23 | HG00140.hp1 HG00280.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.160+24798_160+2479 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43705761 | |||||
| chr11:43705761
|
CTTT | C | 86 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(83): Show | 87 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.160+24797_160+2479 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43705761 | |||||
| chr11:43705761
|
CTTTT | C | 5 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0078others(2): Show | 5 | HG00323.hp2 HG03239.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+24796_160+2479 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43705761 | |||||
| chr11:43705762
|
T | C | 7 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0271others(4): Show | 7 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+24775T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705762 | ||||||
| chr11:43705851
|
T | G | 1 | a0002c0002t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.160+24864T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705851 | ||||||
| chr11:43705861
|
A | T | 1 | a0002c0002t0002g0109 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.160+24874A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705861 | ||||||
| chr11:43705950
|
A | C | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.160+24963A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705950 | ||||||
| chr11:43706026
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.160+25039C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706026 | ||||||
| chr11:43706027
|
G | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+25040G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706027 | ||||||
| chr11:43706191
|
GTTTATC | G | 10 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0003t0001g0198others(7): Show | 10 | HG00639.hp2 HG01069.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+25209_160+2521 others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706191 | |||||
| chr11:43706436
|
T | G | 268 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.160+25449T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706436 | ||||||
| chr11:43706522
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.160+25535A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706522 | ||||||
| chr11:43706661
|
TAGTC | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+25676_160+2567 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706661 | |||||
| chr11:43706689
|
G | GGT | 22 | a0001c0001t0001g0028a0001c0001t0001g0045a0001c0001t0001g0054others(19): Show | 22 | HG00609.hp2 HG02004.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.160+25733_160+2573 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | |||||
| chr11:43706689
|
G | GGTGT | 5 | a0001c0001t0001g0230a0001c0001t0001g0257a0001c0001t0003g0022others(2): Show | 5 | HG00280.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+25731_160+2573 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | |||||
| chr11:43706689
|
G | GGTGTGTG others(1): Show |
8 | a0001c0001t0001g0004a0001c0001t0001g0266a0001c0001t0001g0267others(5): Show | 8 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+25727_160+2573 others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | |||||
| chr11:43706689
|
G | GGTGTGTG others(3): Show |
16 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0003t0001g0198others(13): Show | 16 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+25725_160+2573 others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | |||||
| chr11:43706689
|
G | GGTGTGTG others(5): Show |
58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 58 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.160+25723_160+2573 others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | |||||
| chr11:43706689
|
G | GGTGTGTG others(7): Show |
13 | a0001c0001t0001g0152a0001c0003t0001g0233a0002c0002t0002g0116others(10): Show | 13 | HG00609.hp1 HG01175.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+25721_160+2573 others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | |||||
| chr11:43706689
|
G | GGTGTGTG others(9): Show |
10 | a0001c0001t0001g0005a0001c0003t0003g0245a0001c0003t0003g0247others(7): Show | 10 | HG00323.hp1 HG00408.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.160+25719_160+2573 others(20): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | |||||
| chr11:43706689
|
G | GGTGTGTG others(11): Show |
5 | a0001c0003t0003g0234a0001c0003t0003g0235a0001c0003t0003g0246others(2): Show | 5 | HG02004.hp1 HG02155.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+25717_160+2573 others(22): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | |||||
| chr11:43706689
|
G | GGTGTGTG others(15): Show |
1 | a0001c0003t0003g0249 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.160+25713_160+2573 others(26): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | |||||
| chr11:43706721
|
T | TGTGTGTG others(2): Show |
4 | a0002c0002t0002g0171a0002c0002t0002g0172a0002c0002t0002g0176others(1): Show | 4 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+25734_160+2573 others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706721 | ||||||
| chr11:43706721
|
T | TGTGTGTG others(6): Show |
1 | a0001c0003t0001g0243 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.160+25734_160+2573 others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706721 | ||||||
| chr11:43706724
|
T | TTG | 4 | a0002c0002t0002g0171a0002c0002t0002g0172a0002c0002t0002g0176others(1): Show | 4 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+25737_160+2573 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706724 | ||||||
| chr11:43706780
|
T | C | 91 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(88): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+25793T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706780 | ||||||
| chr11:43706834
|
T | G | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+25847T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706834 | ||||||
| chr11:43706944
|
T | C | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0207 | 3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.160+25957T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706944 | ||||||
| chr11:43706984
|
A | T | 74 | a0001c0001t0001g0152a0001c0001t0001g0187a0002c0002t0002g0003others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.160+25997A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706984 | ||||||
| chr11:43707161
|
G | A | 8 | a0002c0002t0002g0132a0002c0002t0002g0165a0002c0002t0002g0166others(5): Show | 8 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+26174G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43707161 | ||||||
| chr11:43707180
|
T | C | 228 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.160+26193T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43707180 | ||||||
| chr11:43707446
|
C | T | 2 | a0002c0002t0002g0179a0002c0002t0002g0180 | 2 | NA18949.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.160+26459C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43707446 | ||||||
| chr11:43707606
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.160+26619C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43707606 | ||||||
| chr11:43707955
|
A | G | 1 | a0002c0002t0002g0108 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.160+26968A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43707955 | ||||||
| chr11:43708292
|
AAAC | A | 16 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0012others(13): Show | 16 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+27311_160+2731 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43708292 | |||||
| chr11:43708303
|
G | A | 74 | a0001c0001t0001g0152a0001c0001t0001g0187a0002c0002t0002g0003others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.160+27316G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43708303 | ||||||
| chr11:43708437
|
A | G | 74 | a0001c0001t0001g0152a0001c0001t0001g0187a0002c0002t0002g0003others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.160+27450A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43708437 | ||||||
| chr11:43708905
|
G | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+27918G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43708905 | ||||||
| chr11:43709045
|
C | G | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.160+28058C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709045 | ||||||
| chr11:43709195
|
G | T | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+28208G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709195 | ||||||
| chr11:43709270
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.160+28283C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709270 | ||||||
| chr11:43709369
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.160+28382G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709369 | ||||||
| chr11:43709676
|
T | A | 1 | a0001c0001t0001g0029 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.160+28689T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709676 | ||||||
| chr11:43709677
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.160+28690G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709677 | ||||||
| chr11:43709901
|
G | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+28914G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709901 | ||||||
| chr11:43709949
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.160+28962C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709949 | ||||||
| chr11:43709970
|
G | C | 1 | a0001c0001t0001g0037 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.160+28983G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709970 | ||||||
| chr11:43710257
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.160+29270G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43710257 | ||||||
| chr11:43710520
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+29533G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43710520 | ||||||
| chr11:43710678
|
T | C | 1 | a0002c0002t0002g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.160+29691T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43710678 | ||||||
| chr11:43710794
|
T | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+29807T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43710794 | ||||||
| chr11:43710885
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.160+29898G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43710885 | ||||||
| chr11:43710913
|
T | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+29926T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43710913 | ||||||
| chr11:43711032
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.160+30045A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43711032 | ||||||
| chr11:43711314
|
ATATT | A | 4 | a0001c0003t0003g0246a0001c0003t0003g0249a0001c0003t0003g0250others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+30333_160+3033 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43711314 | |||||
| chr11:43711474
|
G | GT | 8 | a0001c0001t0001g0053a0001c0001t0001g0187a0001c0001t0001g0265others(5): Show | 8 | HG01891.hp2 HG02258.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+30505dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43711474 | |||||
| chr11:43711474
|
GT | G | 7 | a0001c0001t0001g0076a0001c0001t0003g0268a0001c0001t0003g0269others(4): Show | 7 | HG01167.hp2 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+30505delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43711474 | |||||
| chr11:43711543
|
C | T | 4 | a0001c0003t0001g0198a0001c0003t0001g0199a0001c0003t0001g0240others(1): Show | 4 | HG01361.hp2 HG03654.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+30556C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43711543 | ||||||
| chr11:43711567
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.160+30580C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43711567 | ||||||
| chr11:43711568
|
G | A | 2 | a0002c0002t0002g0127a0002c0002t0002g0183 | 2 | NA18964.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.160+30581G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43711568 | ||||||
| chr11:43711771
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+30784G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43711771 | ||||||
| chr11:43711819
|
G | A | 1 | a0002c0002t0002g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.160+30832G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43711819 | ||||||
| chr11:43712056
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.160+31069A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712056 | ||||||
| chr11:43712060
|
C | T | 4 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(1): Show | 4 | HG02896.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+31073C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712060 | ||||||
| chr11:43712083
|
A | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+31096A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712083 | ||||||
| chr11:43712200
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0009 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.160+31213G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712200 | ||||||
| chr11:43712296
|
A | G | 22 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.160+31309A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712296 | ||||||
| chr11:43712310
|
C | A | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.160+31323C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712310 | ||||||
| chr11:43712351
|
A | G | 5 | a0001c0001t0001g0031a0001c0001t0001g0203a0001c0001t0001g0204others(2): Show | 5 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+31364A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712351 | ||||||
| chr11:43712404
|
C | T | 13 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(10): Show | 13 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+31417C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712404 | ||||||
| chr11:43712620
|
G | A | 1 | a0002c0002t0002g0162 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.160+31633G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712620 | ||||||
| chr11:43712653
|
T | C | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+31666T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712653 | ||||||
| chr11:43712678
|
C | A | 1 | a0003c0004t0001g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.160+31691C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712678 | ||||||
| chr11:43712711
|
T | C | 250 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.160+31724T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712711 | ||||||
| chr11:43712712
|
G | A | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+31725G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712712 | ||||||
| chr11:43712727
|
G | A | 2 | a0001c0003t0003g0234a0001c0003t0003g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.160+31740G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712727 | ||||||
| chr11:43712994
|
A | G | 1 | a0002c0002t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.160+32007A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712994 | ||||||
| chr11:43713132
|
T | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0009a0002c0002t0002g0202others(1): Show | 4 | HG02257.hp1 HG03098.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+32145T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713132 | ||||||
| chr11:43713279
|
T | TC | 27 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0001g0058others(24): Show | 27 | HG00642.hp1 HG00738.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.160+32298dupC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43713279 | |||||
| chr11:43713582
|
T | G | 5 | a0002c0002t0002g0131a0002c0002t0002g0136a0002c0002t0002g0137others(2): Show | 5 | NA18943.hp2 NA18952.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+32595T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713582 | ||||||
| chr11:43713591
|
G | A | 2 | a0002c0002t0002g0171a0002c0002t0002g0172 | 2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160+32604G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713591 | ||||||
| chr11:43713653
|
A | G | 228 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.160+32666A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713653 | ||||||
| chr11:43713677
|
T | A | 4 | a0002c0002t0002g0116a0002c0002t0002g0117a0002c0002t0002g0118others(1): Show | 4 | HG00408.hp2 HG02135.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+32690T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713677 | ||||||
| chr11:43713697
|
G | A | 4 | a0001c0003t0001g0198a0001c0003t0001g0199a0001c0003t0001g0240others(1): Show | 4 | HG01361.hp2 HG03654.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+32710G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713697 | ||||||
| chr11:43713734
|
G | A | 2 | a0001c0003t0003g0234a0001c0003t0003g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.160+32747G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713734 | ||||||
| chr11:43713762
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.160+32775A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713762 | ||||||
| chr11:43714129
|
T | G | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+33142T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714129 | ||||||
| chr11:43714151
|
G | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+33164G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714151 | ||||||
| chr11:43714191
|
C | T | 1 | a0001c0001t0003g0012 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.160+33204C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714191 | ||||||
| chr11:43714197
|
C | G | 36 | a0001c0001t0001g0187a0002c0002t0002g0003a0002c0002t0002g0108others(33): Show | 36 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.160+33210C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714197 | ||||||
| chr11:43714223
|
C | T | 13 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(10): Show | 13 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+33236C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714223 | ||||||
| chr11:43714528
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+33541C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714528 | ||||||
| chr11:43714599
|
T | C | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 119 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.160+33612T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714599 | ||||||
| chr11:43714874
|
C | A | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+33887C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714874 | ||||||
| chr11:43714996
|
T | G | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.160+34009T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714996 | ||||||
| chr11:43715069
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+34082G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715069 | ||||||
| chr11:43715140
|
C | T | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+34153C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715140 | ||||||
| chr11:43715303
|
A | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+34316A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715303 | ||||||
| chr11:43715472
|
A | G | 1 | a0002c0002t0002g0183 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.160+34485A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715472 | ||||||
| chr11:43715535
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.160+34548T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715535 | ||||||
| chr11:43715549
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.160+34562G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715549 | ||||||
| chr11:43715555
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0045 | 3 | HG01516.hp2 HG02004.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.160+34568A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715555 | ||||||
| chr11:43715566
|
A | G | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 119 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.160+34579A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715566 | ||||||
| chr11:43715584
|
C | A | 1 | a0001c0001t0001g0088 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.160+34597C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715584 | ||||||
| chr11:43715674
|
T | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(34): Show | 37 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.160+34687T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715674 | ||||||
| chr11:43715794
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0003g0022 | 2 | HG00280.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.160+34807C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715794 | ||||||
| chr11:43715803
|
T | G | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.160+34816T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715803 | ||||||
| chr11:43715880
|
C | T | 250 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.160+34893C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715880 | ||||||
| chr11:43715898
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0009 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.160+34911G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715898 | ||||||
| chr11:43715920
|
G | A | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.160+34933G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715920 | ||||||
| chr11:43715951
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161-34960G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715951 | ||||||
| chr11:43716326
|
A | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-34585A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43716326 | ||||||
| chr11:43716450
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.161-34461A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43716450 | ||||||
| chr11:43716470
|
G | A | 2 | a0001c0003t0003g0247a0001c0003t0003g0248 | 2 | HG02004.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.161-34441G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43716470 | ||||||
| chr11:43716505
|
T | C | 1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161-34406T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43716505 | ||||||
| chr11:43716563
|
G | A | 13 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(10): Show | 13 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.161-34348G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43716563 | ||||||
| chr11:43716742
|
C | CAT | 22 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.161-34155_161-3415 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43716742 | |||||
| chr11:43716742
|
CAT | C | 23 | a0002c0002t0002g0128a0002c0002t0002g0139a0002c0002t0002g0140others(20): Show | 23 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-34155_161-3415 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43716742 | |||||
| chr11:43716803
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161-34108T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43716803 | ||||||
| chr11:43717091
|
AG | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0207 | 3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.161-33819delG | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717091 | ||||||
| chr11:43717248
|
T | C | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-33663T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717248 | ||||||
| chr11:43717397
|
A | G | 3 | a0001c0001t0001g0053a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG02165.hp2 HG03831.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.161-33514A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717397 | ||||||
| chr11:43717547
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.161-33364T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717547 | ||||||
| chr11:43717646
|
C | T | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-33265C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717646 | ||||||
| chr11:43717804
|
C | CT | 33 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0001t0001g0080others(30): Show | 33 | HG00642.hp2 HG01069.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.161-33089dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43717804 | |||||
| chr11:43717804
|
CT | C | 77 | a0001c0001t0001g0152a0001c0001t0001g0187a0001c0001t0001g0196others(74): Show | 77 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.161-33089delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43717804 | |||||
| chr11:43717804
|
CTT | C | 9 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0271others(6): Show | 9 | HG01515.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-33090_161-3308 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43717804 | |||||
| chr11:43717886
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.161-33025C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717886 | ||||||
| chr11:43717927
|
C | A | 4 | a0002c0002t0002g0116a0002c0002t0002g0117a0002c0002t0002g0118others(1): Show | 4 | HG00408.hp2 HG02135.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-32984C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717927 | ||||||
| chr11:43718051
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.161-32860C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718051 | ||||||
| chr11:43718101
|
G | A | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161-32810G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718101 | ||||||
| chr11:43718307
|
G | A | 78 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(75): Show | 79 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.161-32604G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718307 | ||||||
| chr11:43718353
|
G | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0126 | 3 | HG01884.hp2 HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-32558G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718353 | ||||||
| chr11:43718715
|
A | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-32196A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718715 | ||||||
| chr11:43718723
|
A | G | 3 | a0002c0002t0002g0254a0002c0002t0002g0255a0002c0002t0002g0256 | 3 | HG01891.hp1 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.161-32188A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718723 | ||||||
| chr11:43718832
|
C | T | 5 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(2): Show | 5 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-32079C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718832 | ||||||
| chr11:43718839
|
G | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161-32072G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718839 | ||||||
| chr11:43718872
|
T | C | 228 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.161-32039T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718872 | ||||||
| chr11:43718990
|
C | A | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.161-31921C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718990 | ||||||
| chr11:43719615
|
CA | C | 12 | a0001c0001t0001g0230a0001c0001t0003g0268a0001c0001t0003g0269others(9): Show | 12 | HG01070.hp1 HG02451.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.161-31283delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43719615 | |||||
| chr11:43719615
|
CAA | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(13): Show | 16 | HG01261.hp2 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.161-31284_161-3128 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43719615 | |||||
| chr11:43719625
|
A | AT | 4 | a0001c0001t0001g0096a0001c0001t0001g0203a0001c0001t0001g0204others(1): Show | 4 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-31286_161-3128 others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719625 | ||||||
| chr11:43719625
|
A | T | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.161-31286A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719625 | ||||||
| chr11:43719626
|
AAAT | A | 19 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0003t0001g0198others(16): Show | 19 | HG00423.hp1 HG00639.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.161-31283_161-3128 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43719626 | |||||
| chr11:43719627
|
A | AT | 23 | a0001c0001t0001g0058a0001c0001t0001g0062a0001c0001t0001g0068others(20): Show | 23 | HG00280.hp1 HG00609.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-31284_161-3128 others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719627 | ||||||
| chr11:43719627
|
A | T | 57 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0032others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(54): Show |
intron_variant | MODIFIER | c.161-31284A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719627 | ||||||
| chr11:43719627
|
AAT | A | 62 | a0001c0001t0001g0152a0001c0003t0001g0233a0001c0003t0003g0234others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.161-31268_161-3126 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43719627 | |||||
| chr11:43719629
|
T | A | 6 | a0001c0001t0001g0048a0001c0001t0001g0120a0002c0002t0002g0001others(3): Show | 7 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-31282T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719629 | ||||||
| chr11:43719631
|
T | A | 4 | a0002c0002t0002g0171a0002c0002t0002g0172a0002c0002t0002g0178others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-31280T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719631 | ||||||
| chr11:43719947
|
G | A | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-30964G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719947 | ||||||
| chr11:43719980
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.161-30931T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719980 | ||||||
| chr11:43720106
|
ATCTTATG others(8): Show |
A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0207 | 3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.161-30801_161-3078 others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43720106 | |||||
| chr11:43720145
|
A | G | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(31): Show | 34 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.161-30766A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720145 | ||||||
| chr11:43720170
|
G | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161-30741G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720170 | ||||||
| chr11:43720262
|
T | C | 268 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.161-30649T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720262 | ||||||
| chr11:43720391
|
G | T | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(31): Show | 34 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.161-30520G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720391 | ||||||
| chr11:43720616
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.161-30295G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720616 | ||||||
| chr11:43720806
|
G | A | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.161-30105G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720806 | ||||||
| chr11:43720816
|
TA | T | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 116 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.161-30094delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720816 | ||||||
| chr11:43720849
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.161-30062A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720849 | ||||||
| chr11:43720851
|
A | C | 1 | a0002c0002t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.161-30060A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720851 | ||||||
| chr11:43720927
|
A | T | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 119 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.161-29984A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720927 | ||||||
| chr11:43721197
|
G | C | 1 | a0001c0001t0001g0103 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.161-29714G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721197 | ||||||
| chr11:43721280
|
C | G | 1 | a0001c0003t0001g0273 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.161-29631C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721280 | ||||||
| chr11:43721280
|
C | T | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 116 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.161-29631C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721280 | ||||||
| chr11:43721347
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.161-29564C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721347 | ||||||
| chr11:43721573
|
C | T | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-29338C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721573 | ||||||
| chr11:43721752
|
T | C | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(119): Show | 122 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.161-29159T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721752 | ||||||
| chr11:43721834
|
G | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-29077G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721834 | ||||||
| chr11:43721857
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-29054C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721857 | ||||||
| chr11:43721948
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161-28963A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721948 | ||||||
| chr11:43722136
|
C | G | 8 | a0002c0002t0002g0003a0002c0002t0002g0144a0002c0002t0002g0145others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-28775C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722136 | ||||||
| chr11:43722229
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.161-28682A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722229 | ||||||
| chr11:43722452
|
C | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0126 | 3 | HG01884.hp2 HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-28459C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722452 | ||||||
| chr11:43722608
|
A | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0045 | 2 | HG02004.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.161-28303A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722608 | ||||||
| chr11:43722771
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.161-28140C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722771 | ||||||
| chr11:43722773
|
C | T | 1 | a0002c0002t0002g0163 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.161-28138C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722773 | ||||||
| chr11:43722797
|
C | T | 2 | a0002c0002t0002g0138a0002c0002t0007g0146 | 2 | HG01109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.161-28114C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722797 | ||||||
| chr11:43722833
|
G | GA | 236 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(233): Show | 237 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.161-28068dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43722833 | |||||
| chr11:43722966
|
C | T | 2 | a0002c0002t0002g0161a0002c0002t0002g0164 | 2 | HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.161-27945C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722966 | ||||||
| chr11:43722982
|
G | T | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0271 | 3 | HG02451.hp2 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.161-27929G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722982 | ||||||
| chr11:43722997
|
A | T | 2 | a0001c0001t0003g0019a0005c0006t0012g0020 | 2 | HG00609.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.161-27914A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722997 | ||||||
| chr11:43723346
|
G | C | 2 | a0002c0002t0002g0150a0002c0002t0002g0160 | 2 | HG00609.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.161-27565G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43723346 | ||||||
| chr11:43723574
|
T | C | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-27337T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43723574 | ||||||
| chr11:43723615
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.161-27296A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43723615 | ||||||
| chr11:43723617
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-27294G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43723617 | ||||||
| chr11:43723906
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.161-27005C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43723906 | ||||||
| chr11:43723962
|
AT | A | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.161-26938delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43723962 | |||||
| chr11:43724014
|
A | G | 90 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(87): Show | 91 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.161-26897A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724014 | ||||||
| chr11:43724025
|
A | C | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161-26886A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724025 | ||||||
| chr11:43724042
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.161-26869C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724042 | ||||||
| chr11:43724057
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0207 | 3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.161-26854G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724057 | ||||||
| chr11:43724219
|
C | CTG | 71 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0046others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.161-26652_161-2665 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | |||||
| chr11:43724219
|
C | CTGTG | 41 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0059others(38): Show | 41 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.161-26654_161-2665 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | |||||
| chr11:43724219
|
C | CTGTGTG | 15 | a0001c0001t0001g0062a0001c0001t0001g0114a0001c0001t0001g0221others(12): Show | 15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-26656_161-2665 others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | |||||
| chr11:43724219
|
C | CTGTGTGT others(3): Show |
3 | a0001c0003t0001g0237a0001c0003t0001g0239a0002c0002t0002g0157 | 3 | HG00639.hp2 HG01106.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.161-26660_161-2665 others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | |||||
| chr11:43724219
|
CTG | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0210a0001c0001t0001g0211others(11): Show | 14 | HG01099.hp2 HG01106.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.161-26652_161-2665 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | |||||
| chr11:43724219
|
CTGTG | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0077a0001c0001t0001g0083others(4): Show | 7 | HG00423.hp2 HG01123.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-26654_161-2665 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | |||||
| chr11:43724219
|
CTGTGTGT others(1): Show |
C | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0003t0003g0246 | 3 | HG02895.hp1 HG02897.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.161-26658_161-2665 others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | |||||
| chr11:43724219
|
CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0001g0203 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-26660_161-2665 others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | |||||
| chr11:43724219
|
CTGTGTGT others(7): Show |
C | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-26664_161-2665 others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | |||||
| chr11:43724245
|
G | C | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.161-26666G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724245 | ||||||
| chr11:43724260
|
T | TGTGTGTG others(4): Show |
1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161-26651_161-2665 others(15): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724260 | ||||||
| chr11:43724492
|
G | A | 1 | a0002c0002t0002g0163 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.161-26419G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724492 | ||||||
| chr11:43724526
|
AC | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-26384delC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724526 | ||||||
| chr11:43724541
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.161-26370A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724541 | ||||||
| chr11:43724685
|
C | T | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.161-26226C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724685 | ||||||
| chr11:43724699
|
T | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-26212T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724699 | ||||||
| chr11:43724759
|
A | G | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG00099.hp2 HG01168.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.161-26152A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724759 | ||||||
| chr11:43724988
|
C | T | 1 | a0002c0002t0002g0116 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.161-25923C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724988 | ||||||
| chr11:43725044
|
A | G | 91 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(88): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.161-25867A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43725044 | ||||||
| chr11:43725330
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.161-25581G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43725330 | ||||||
| chr11:43725352
|
T | G | 9 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(6): Show | 9 | NA18612.hp2 NA18747.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-25559T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43725352 | ||||||
| chr11:43725449
|
G | A | 278 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.161-25462G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43725449 | ||||||
| chr11:43725845
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-25066G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43725845 | ||||||
| chr11:43725854
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161-25057G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43725854 | ||||||
| chr11:43725882
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.161-25029G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43725882 | ||||||
| chr11:43726004
|
A | T | 17 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0012others(14): Show | 17 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.161-24907A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726004 | ||||||
| chr11:43726165
|
T | G | 4 | a0002c0002t0002g0253a0002c0002t0002g0254a0002c0002t0002g0255others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-24746T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726165 | ||||||
| chr11:43726250
|
G | A | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 126 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.161-24661G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726250 | ||||||
| chr11:43726362
|
A | G | 84 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.161-24549A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726362 | ||||||
| chr11:43726445
|
A | T | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-24466A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726445 | ||||||
| chr11:43726560
|
T | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-24351T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726560 | ||||||
| chr11:43726734
|
T | C | 12 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(9): Show | 12 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.161-24177T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726734 | ||||||
| chr11:43726835
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00738.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.161-24076A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726835 | ||||||
| chr11:43726879
|
A | G | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161-24032A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726879 | ||||||
| chr11:43727033
|
T | C | 3 | a0001c0003t0003g0234a0001c0003t0003g0235a0002c0002t0002g0155 | 3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.161-23878T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727033 | ||||||
| chr11:43727069
|
A | G | 15 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-23842A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727069 | ||||||
| chr11:43727123
|
C | T | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.161-23788C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727123 | ||||||
| chr11:43727203
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0003g0207a0003c0004t0001g0252 | 3 | HG02055.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.161-23708C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727203 | ||||||
| chr11:43727210
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.161-23701T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727210 | ||||||
| chr11:43727490
|
CT | C | 233 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.161-23409delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43727490 | |||||
| chr11:43727569
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.161-23342C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727569 | ||||||
| chr11:43727589
|
G | T | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161-23322G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727589 | ||||||
| chr11:43727649
|
A | G | 110 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(107): Show | 110 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.161-23262A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727649 | ||||||
| chr11:43728022
|
A | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-22889A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728022 | ||||||
| chr11:43728038
|
T | A | 52 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 52 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.161-22873T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728038 | ||||||
| chr11:43728222
|
C | T | 18 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0012others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-22689C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728222 | ||||||
| chr11:43728348
|
A | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-22563A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728348 | ||||||
| chr11:43728402
|
T | A | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.161-22509T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728402 | ||||||
| chr11:43728450
|
T | C | 1 | a0001c0001t0003g0022 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.161-22461T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728450 | ||||||
| chr11:43728476
|
T | TA | 18 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0012others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-22425dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43728476 | |||||
| chr11:43728533
|
C | A | 1 | a0001c0001t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161-22378C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728533 | ||||||
| chr11:43728718
|
C | T | 6 | a0002c0002t0002g0003a0002c0002t0002g0145a0002c0002t0002g0153others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-22193C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728718 | ||||||
| chr11:43728826
|
G | A | 6 | a0001c0003t0001g0198a0001c0003t0001g0199a0001c0003t0001g0236others(3): Show | 6 | HG01069.hp1 HG01361.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-22085G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728826 | ||||||
| chr11:43729252
|
T | C | 18 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0012others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-21659T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43729252 | ||||||
| chr11:43729434
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.161-21477A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43729434 | ||||||
| chr11:43729536
|
T | C | 18 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0012others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-21375T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43729536 | ||||||
| chr11:43729600
|
G | A | 2 | a0001c0003t0001g0226a0001c0003t0001g0273 | 2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.161-21311G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43729600 | ||||||
| chr11:43729649
|
T | C | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0207 | 3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.161-21262T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43729649 | ||||||
| chr11:43729762
|
A | G | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.161-21149A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43729762 | ||||||
| chr11:43730014
|
A | AT | 23 | a0001c0001t0001g0008a0001c0001t0001g0187a0001c0001t0001g0209others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.161-20896dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43730014 | |||||
| chr11:43730022
|
T | C | 1 | a0002c0002t0002g0140 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.161-20889T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730022 | ||||||
| chr11:43730040
|
G | C | 7 | a0002c0002t0002g0165a0002c0002t0002g0166a0002c0002t0002g0167others(4): Show | 7 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-20871G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730040 | ||||||
| chr11:43730048
|
T | G | 13 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0003t0001g0198others(10): Show | 13 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-20863T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730048 | ||||||
| chr11:43730304
|
G | T | 3 | a0002c0002t0004g0206a0002c0002t0004g0275a0002c0002t0009g0201 | 3 | HG02451.hp1 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.161-20607G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730304 | ||||||
| chr11:43730359
|
G | A | 1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161-20552G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730359 | ||||||
| chr11:43730746
|
C | T | 3 | a0002c0002t0002g0188a0002c0002t0002g0189a0002c0002t0002g0190 | 3 | HG00140.hp2 HG01167.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.161-20165C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730746 | ||||||
| chr11:43730965
|
A | G | 1 | a0002c0002t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.161-19946A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730965 | ||||||
| chr11:43730972
|
G | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-19939G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730972 | ||||||
| chr11:43730983
|
A | G | 19 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0012others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.161-19928A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730983 | ||||||
| chr11:43730998
|
T | C | 18 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0012others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-19913T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730998 | ||||||
| chr11:43731089
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG03453.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.161-19822C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731089 | ||||||
| chr11:43731098
|
G | C | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-19813G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731098 | ||||||
| chr11:43731439
|
C | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-19472C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731439 | ||||||
| chr11:43731564
|
T | A | 19 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0266others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.161-19347T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731564 | ||||||
| chr11:43731643
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.161-19268G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731643 | ||||||
| chr11:43731914
|
C | T | 18 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0012others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-18997C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731914 | ||||||
| chr11:43731963
|
G | A | 1 | a0001c0003t0001g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-18948G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731963 | ||||||
| chr11:43732111
|
G | C | 19 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0266others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.161-18800G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43732111 | ||||||
| chr11:43732175
|
G | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-18736G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43732175 | ||||||
| chr11:43732272
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161-18639G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43732272 | ||||||
| chr11:43732610
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-18301G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43732610 | ||||||
| chr11:43732822
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-18089A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43732822 | ||||||
| chr11:43732830
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.161-18081T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43732830 | ||||||
| chr11:43733059
|
C | A | 13 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-17852C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733059 | ||||||
| chr11:43733498
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.161-17413A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733498 | ||||||
| chr11:43733527
|
C | T | 2 | a0001c0003t0003g0234a0001c0003t0003g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.161-17384C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733527 | ||||||
| chr11:43733551
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161-17360G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733551 | ||||||
| chr11:43733594
|
A | G | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-17317A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733594 | ||||||
| chr11:43733682
|
T | A | 13 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-17229T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733682 | ||||||
| chr11:43733796
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.161-17115G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733796 | ||||||
| chr11:43733868
|
C | A | 1 | a0001c0001t0001g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.161-17043C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733868 | ||||||
| chr11:43733888
|
G | A | 5 | a0002c0002t0002g0171a0002c0002t0002g0172a0002c0002t0002g0176others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-17023G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733888 | ||||||
| chr11:43734107
|
T | G | 1 | a0002c0002t0002g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.161-16804T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734107 | ||||||
| chr11:43734174
|
C | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-16737C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734174 | ||||||
| chr11:43734230
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.161-16681C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734230 | ||||||
| chr11:43734293
|
A | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-16618A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734293 | ||||||
| chr11:43734294
|
G | T | 1 | a0002c0002t0006g0107 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.161-16617G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734294 | ||||||
| chr11:43734380
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.161-16531C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734380 | ||||||
| chr11:43734411
|
G | C | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161-16500G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734411 | ||||||
| chr11:43734578
|
T | A | 2 | a0002c0002t0002g0127a0002c0002t0002g0183 | 2 | NA18964.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.161-16333T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734578 | ||||||
| chr11:43734601
|
T | TG | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-16308dupG | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43734601 | |||||
| chr11:43734777
|
C | G | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161-16134C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734777 | ||||||
| chr11:43734839
|
C | G | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-16072C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734839 | ||||||
| chr11:43734886
|
A | T | 5 | a0002c0002t0002g0171a0002c0002t0002g0172a0002c0002t0002g0176others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-16025A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734886 | ||||||
| chr11:43734910
|
C | T | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-16001C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734910 | ||||||
| chr11:43734928
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0009 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.161-15983T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734928 | ||||||
| chr11:43735321
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.161-15590G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43735321 | ||||||
| chr11:43735334
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0009 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.161-15577A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43735334 | ||||||
| chr11:43735471
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161-15440A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43735471 | ||||||
| chr11:43735967
|
T | C | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-14944T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43735967 | ||||||
| chr11:43736220
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.161-14691G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43736220 | ||||||
| chr11:43736432
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0041 | 3 | HG02257.hp1 NA18522.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.161-14479C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43736432 | ||||||
| chr11:43737102
|
C | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-13809C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737102 | ||||||
| chr11:43737388
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0104 | 2 | HG01928.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.161-13523G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737388 | ||||||
| chr11:43737397
|
C | T | 2 | a0002c0002t0002g0166a0002c0002t0002g0167 | 2 | HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.161-13514C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737397 | ||||||
| chr11:43737621
|
T | A | 1 | a0001c0001t0001g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.161-13290T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737621 | ||||||
| chr11:43737772
|
A | G | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-13139A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737772 | ||||||
| chr11:43737840
|
G | A | 1 | a0001c0003t0001g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.161-13071G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737840 | ||||||
| chr11:43737940
|
G | A | 8 | a0002c0002t0002g0128a0002c0002t0002g0140a0002c0002t0002g0147others(5): Show | 8 | HG00140.hp2 HG01070.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-12971G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737940 | ||||||
| chr11:43737945
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-12966C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737945 | ||||||
| chr11:43737966
|
G | A | 23 | a0001c0001t0001g0008a0001c0001t0001g0187a0001c0001t0001g0209others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.161-12945G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737966 | ||||||
| chr11:43737998
|
G | T | 1 | a0001c0001t0001g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.161-12913G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737998 | ||||||
| chr11:43738000
|
C | G | 1 | a0001c0001t0001g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.161-12911C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43738000 | ||||||
| chr11:43738001
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.161-12910A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43738001 | ||||||
| chr11:43738056
|
C | CA | 41 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0046others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.161-12835dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43738056 | |||||
| chr11:43738056
|
CA | C | 59 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(56): Show | 59 | HG00280.hp2 HG00423.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.161-12835delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43738056 | |||||
| chr11:43738056
|
CAA | C | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-12836_161-1283 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43738056 | |||||
| chr11:43738075
|
AAT | A | 12 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(9): Show | 12 | HG01496.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.161-12834_161-1283 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43738075 | |||||
| chr11:43738076
|
AT | A | 5 | a0001c0001t0001g0123a0001c0001t0001g0258a0001c0001t0001g0259others(2): Show | 5 | HG01109.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-12834delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43738076 | ||||||
| chr11:43738118
|
AAGCATGT others(18): Show |
A | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.161-12783_161-1275 others(29): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43738118 | |||||
| chr11:43738338
|
T | G | 1 | a0001c0001t0003g0019 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.161-12573T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43738338 | ||||||
| chr11:43738385
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.161-12526C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43738385 | ||||||
| chr11:43738665
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0045 | 3 | HG01516.hp2 HG02004.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.161-12246C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43738665 | ||||||
| chr11:43739009
|
T | G | 2 | a0002c0002t0008g0002a0002c0002t0009g0201 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.161-11902T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739009 | ||||||
| chr11:43739057
|
A | G | 98 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(95): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.161-11854A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739057 | ||||||
| chr11:43739070
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.161-11841G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739070 | ||||||
| chr11:43739084
|
C | G | 3 | a0002c0002t0002g0148a0002c0002t0002g0149a0002c0002t0006g0107 | 3 | HG00735.hp1 NA18941.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.161-11827C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739084 | ||||||
| chr11:43739185
|
G | T | 98 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(95): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.161-11726G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739185 | ||||||
| chr11:43739240
|
G | A | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-11671G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739240 | ||||||
| chr11:43739563
|
C | G | 1 | a0002c0002t0002g0178 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.161-11348C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739563 | ||||||
| chr11:43739701
|
T | TC | 222 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.161-11210_161-1120 others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739701 | ||||||
| chr11:43740075
|
C | T | 5 | a0002c0002t0002g0171a0002c0002t0002g0172a0002c0002t0002g0176others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-10836C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740075 | ||||||
| chr11:43740164
|
A | T | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-10747A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740164 | ||||||
| chr11:43740239
|
G | T | 1 | a0002c0002t0006g0107 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.161-10672G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740239 | ||||||
| chr11:43740242
|
C | T | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-10669C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740242 | ||||||
| chr11:43740267
|
C | T | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-10644C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740267 | ||||||
| chr11:43740459
|
A | G | 22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.161-10452A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740459 | ||||||
| chr11:43740660
|
A | G | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.161-10251A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740660 | ||||||
| chr11:43740945
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.161-9966C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740945 | ||||||
| chr11:43741000
|
G | A | 1 | a0001c0001t0003g0012 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.161-9911G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741000 | ||||||
| chr11:43741154
|
A | G | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-9757A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741154 | ||||||
| chr11:43741336
|
C | T | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0203others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-9575C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741336 | ||||||
| chr11:43741455
|
T | TA | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-9447dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43741455 | |||||
| chr11:43741803
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.161-9108G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741803 | ||||||
| chr11:43741819
|
C | T | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-9092C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741819 | ||||||
| chr11:43741820
|
C | T | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-9091C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741820 | ||||||
| chr11:43741915
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG03453.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.161-8996T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741915 | ||||||
| chr11:43742019
|
C | G | 1 | a0001c0001t0001g0009 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.161-8892C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742019 | ||||||
| chr11:43742112
|
A | AAT | 5 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0054others(2): Show | 5 | HG00099.hp1 HG00323.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-8772_161-8771d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742112 | |||||
| chr11:43742112
|
AAT | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0110a0001c0001t0001g0111others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-8772_161-8771d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742112 | |||||
| chr11:43742112
|
AATAT | A | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.161-8774_161-8771d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742112 | |||||
| chr11:43742112
|
AATATAT | A | 3 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195 | 3 | HG02559.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.161-8776_161-8771d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742112 | |||||
| chr11:43742132
|
TATA | T | 21 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(18): Show | 21 | HG01109.hp1 HG01361.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-8778_161-8776d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742132 | ||||||
| chr11:43742134
|
TATA | T | 15 | a0001c0001t0001g0272a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG06807.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-8776_161-8774d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742134 | ||||||
| chr11:43742135
|
A | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0259a0002c0002t0002g0127others(1): Show | 4 | HG01891.hp2 HG02922.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-8776A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742135 | ||||||
| chr11:43742137
|
A | ATT | 12 | a0001c0001t0001g0033a0001c0001t0001g0045a0001c0001t0001g0058others(9): Show | 12 | HG01346.hp2 HG01358.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.161-8773_161-8772i others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742137 | |||||
| chr11:43742137
|
A | T | 88 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.161-8774A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742137 | ||||||
| chr11:43742139
|
A | AT | 5 | a0002c0002t0002g0151a0002c0002t0002g0171a0002c0002t0002g0172others(2): Show | 5 | HG02723.hp1 HG03130.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-8761dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742139 | |||||
| chr11:43742139
|
A | ATATATAT others(3): Show |
3 | a0001c0003t0003g0247a0001c0003t0003g0248a0002c0002t0002g0160 | 3 | HG02004.hp1 HG02155.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.161-8771_161-8770i others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742139 | |||||
| chr11:43742139
|
A | ATATATAT others(5): Show |
1 | a0002c0002t0004g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161-8771_161-8770i others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742139 | |||||
| chr11:43742139
|
A | ATATATTT others(1): Show |
6 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0249others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-8771_161-8770i others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742139 | |||||
| chr11:43742139
|
A | ATATT | 8 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0049others(5): Show | 8 | HG00738.hp2 HG01123.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-8771_161-8770i others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742139 | |||||
| chr11:43742139
|
A | ATT | 59 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(56): Show | 59 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.161-8762_161-8761d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742139 | |||||
| chr11:43742139
|
A | T | 168 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(165): Show | 169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.161-8772A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742139 | ||||||
| chr11:43742140
|
T | TATATATA others(2): Show |
4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-8771_161-8770i others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742140 | ||||||
| chr11:43742141
|
T | A | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161-8770T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742141 | ||||||
| chr11:43742142
|
T | A | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-8769T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742142 | ||||||
| chr11:43742151
|
A | T | 1 | a0001c0001t0001g0197 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.161-8760A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742151 | ||||||
| chr11:43742531
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0052 | 3 | HG02135.hp2 NA19070.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.161-8380T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742531 | ||||||
| chr11:43742752
|
G | T | 19 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0203others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.161-8159G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742752 | ||||||
| chr11:43742754
|
G | T | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-8157G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742754 | ||||||
| chr11:43742756
|
G | T | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-8155G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742756 | ||||||
| chr11:43742758
|
G | GT | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-8152dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742758 | |||||
| chr11:43742760
|
G | GT | 9 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 9 | HG01175.hp2 HG01884.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-8141dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742760 | |||||
| chr11:43742760
|
G | T | 16 | a0001c0001t0001g0081a0001c0001t0003g0012a0001c0001t0003g0013others(13): Show | 16 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.161-8151G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742760 | ||||||
| chr11:43742762
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.161-8149T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742762 | ||||||
| chr11:43742790
|
A | G | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-8121A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742790 | ||||||
| chr11:43743033
|
A | G | 4 | a0002c0002t0002g0001a0002c0002t0002g0026a0002c0002t0002g0057others(1): Show | 5 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-7878A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43743033 | ||||||
| chr11:43743260
|
T | G | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-7651T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43743260 | ||||||
| chr11:43743372
|
T | C | 1 | a0005c0006t0012g0020 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.161-7539T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43743372 | ||||||
| chr11:43743436
|
A | C | 1 | a0001c0001t0001g0058 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.161-7475A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43743436 | ||||||
| chr11:43744139
|
T | G | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161-6772T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43744139 | ||||||
| chr11:43744356
|
T | TA | 26 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(23): Show | 26 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-6545dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43744356 | |||||
| chr11:43744400
|
G | A | 23 | a0001c0001t0001g0008a0001c0001t0001g0187a0001c0001t0001g0209others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.161-6511G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43744400 | ||||||
| chr11:43744640
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.161-6271C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43744640 | ||||||
| chr11:43744764
|
A | T | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-6147A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43744764 | ||||||
| chr11:43744784
|
G | T | 13 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(10): Show | 13 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-6127G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43744784 | ||||||
| chr11:43745274
|
G | A | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-5637G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43745274 | ||||||
| chr11:43745352
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-5559T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43745352 | ||||||
| chr11:43745480
|
A | G | 1 | a0001c0003t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.161-5431A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43745480 | ||||||
| chr11:43745964
|
C | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-4947C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43745964 | ||||||
| chr11:43746000
|
A | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.161-4911A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746000 | ||||||
| chr11:43746034
|
A | G | 2 | a0001c0003t0003g0234a0001c0003t0003g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.161-4877A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746034 | ||||||
| chr11:43746246
|
T | C | 112 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.161-4665T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746246 | ||||||
| chr11:43746301
|
A | G | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.161-4610A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746301 | ||||||
| chr11:43746649
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161-4262G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746649 | ||||||
| chr11:43746704
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-4207A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746704 | ||||||
| chr11:43746928
|
T | G | 11 | a0002c0002t0002g0003a0002c0002t0002g0138a0002c0002t0002g0142others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-3983T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746928 | ||||||
| chr11:43746933
|
A | G | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-3978A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746933 | ||||||
| chr11:43747656
|
C | G | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-3255C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43747656 | ||||||
| chr11:43747675
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00738.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.161-3236G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43747675 | ||||||
| chr11:43747737
|
A | C | 93 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(90): Show | 93 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.161-3174A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43747737 | ||||||
| chr11:43747745
|
C | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-3166C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43747745 | ||||||
| chr11:43747880
|
GC | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-3026delC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43747880 | |||||
| chr11:43748041
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.161-2870C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43748041 | ||||||
| chr11:43748138
|
G | A | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.161-2773G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43748138 | ||||||
| chr11:43748419
|
G | A | 1 | a0001c0003t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.161-2492G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43748419 | ||||||
| chr11:43748518
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.161-2393C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43748518 | ||||||
| chr11:43749375
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.161-1536C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43749375 | ||||||
| chr11:43749443
|
C | T | 2 | a0001c0003t0001g0198a0001c0003t0001g0199 | 2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.161-1468C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43749443 | ||||||
| chr11:43749534
|
A | G | 98 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(95): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.161-1377A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43749534 | ||||||
| chr11:43749552
|
A | T | 1 | a0001c0001t0003g0015 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.161-1359A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43749552 | ||||||
| chr11:43749573
|
G | A | 2 | a0002c0002t0002g0171a0002c0002t0002g0172 | 2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.161-1338G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43749573 | ||||||
| chr11:43749969
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.161-942C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43749969 | ||||||
| chr11:43750264
|
T | A | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.161-647T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750264 | ||||||
| chr11:43750265
|
T | A | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.161-646T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750265 | ||||||
| chr11:43750463
|
A | G | 1 | a0002c0002t0002g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.161-448A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750463 | ||||||
| chr11:43750519
|
T | C | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.161-392T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750519 | ||||||
| chr11:43750557
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-354A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750557 | ||||||
| chr11:43750680
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.161-231G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750680 | ||||||
| chr11:43750868
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.161-43A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750868 | ||||||
| chr11:43750999
|
A | G | 76 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(73): Show | 76 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.207+42A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43750999 | ||||||
| chr11:43751559
|
G | T | 1 | a0001c0001t0001g0041 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.207+602G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43751559 | ||||||
| chr11:43751759
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.207+802T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43751759 | ||||||
| chr11:43751834
|
T | C | 3 | a0002c0002t0004g0206a0002c0002t0004g0275a0002c0002t0009g0201 | 3 | HG02451.hp1 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.207+877T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43751834 | ||||||
| chr11:43751857
|
T | G | 1 | a0001c0001t0001g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.207+900T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43751857 | ||||||
| chr11:43751955
|
C | T | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.207+998C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43751955 | ||||||
| chr11:43752158
|
C | T | 3 | a0002c0002t0002g0181a0004c0005t0002g0010a0004c0005t0002g0011 | 3 | HG01099.hp2 HG01106.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.207+1201C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752158 | ||||||
| chr11:43752263
|
T | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.207+1306T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752263 | ||||||
| chr11:43752283
|
C | T | 1 | a0002c0002t0002g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.207+1326C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752283 | ||||||
| chr11:43752609
|
G | A | 1 | a0002c0002t0002g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.208-1437G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752609 | ||||||
| chr11:43752724
|
A | G | 98 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(95): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.208-1322A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752724 | ||||||
| chr11:43752881
|
C | T | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.208-1165C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752881 | ||||||
| chr11:43752942
|
A | G | 1 | a0002c0002t0002g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208-1104A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752942 | ||||||
| chr11:43752992
|
A | G | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.208-1054A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752992 | ||||||
| chr11:43753126
|
G | A | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.208-920G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753126 | ||||||
| chr11:43753181
|
C | T | 13 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.208-865C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753181 | ||||||
| chr11:43753318
|
T | C | 1 | a0001c0003t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.208-728T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753318 | ||||||
| chr11:43753384
|
CT | C | 275 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.208-644delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 43753384 | |||||
| chr11:43753474
|
A | G | 278 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.208-572A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753474 | ||||||
| chr11:43753557
|
TA | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0221a0001c0001t0001g0259others(8): Show | 11 | HG01261.hp2 HG01496.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-473delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 43753557 | |||||
| chr11:43753557
|
TAAA | T | 11 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(8): Show | 11 | HG02258.hp1 NA18612.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-475_208-473del others(3): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 43753557 | |||||
| chr11:43753627
|
T | C | 2 | a0001c0001t0003g0207a0002c0002t0002g0003 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.208-419T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753627 | ||||||
| chr11:43753815
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.208-231G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753815 | ||||||
| chr11:43753869
|
A | C | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.208-177A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753869 | ||||||
| chr11:43753970
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.208-76A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753970 | ||||||
| chr11:43754184
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+63A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43754184 | ||||||
| chr11:43754333
|
G | A | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0271 | 3 | HG02451.hp2 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.283+212G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43754333 | ||||||
| chr11:43754435
|
G | A | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283+314G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43754435 | ||||||
| chr11:43754538
|
T | A | 1 | a0001c0003t0003g0246 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.283+417T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43754538 | ||||||
| chr11:43754739
|
A | C | 7 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+618A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43754739 | ||||||
| chr11:43754931
|
C | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+810C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43754931 | ||||||
| chr11:43755246
|
G | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+1125G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43755246 | ||||||
| chr11:43755790
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.283+1669G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43755790 | ||||||
| chr11:43755828
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.283+1707G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43755828 | ||||||
| chr11:43755847
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.283+1726G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43755847 | ||||||
| chr11:43755934
|
G | A | 98 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(95): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.283+1813G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43755934 | ||||||
| chr11:43755950
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.283+1829G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43755950 | ||||||
| chr11:43756179
|
C | T | 2 | a0001c0003t0003g0247a0001c0003t0003g0248 | 2 | HG02004.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.283+2058C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43756179 | ||||||
| chr11:43756217
|
CT | C | 16 | a0001c0001t0001g0257a0001c0001t0003g0012a0001c0001t0003g0013others(13): Show | 16 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+2109delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43756217 | |||||
| chr11:43756230
|
T | A | 15 | a0001c0001t0001g0009a0001c0001t0001g0091a0001c0001t0003g0268others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+2109T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43756230 | ||||||
| chr11:43756670
|
A | G | 2 | a0001c0003t0003g0234a0001c0003t0003g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.283+2549A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43756670 | ||||||
| chr11:43757060
|
T | C | 37 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(34): Show | 37 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.283+2939T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757060 | ||||||
| chr11:43757315
|
G | T | 1 | a0001c0001t0001g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.283+3194G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757315 | ||||||
| chr11:43757572
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.283+3451G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757572 | ||||||
| chr11:43757609
|
C | T | 7 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+3488C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757609 | ||||||
| chr11:43757627
|
G | A | 19 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0266others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.283+3506G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757627 | ||||||
| chr11:43757639
|
C | CA | 72 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0037others(69): Show | 72 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.283+3546dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | |||||
| chr11:43757639
|
C | CAA | 48 | a0001c0001t0001g0038a0001c0001t0001g0075a0001c0001t0001g0105others(45): Show | 49 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.283+3545_283+3546d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | |||||
| chr11:43757639
|
C | CAAA | 14 | a0001c0001t0001g0259a0001c0001t0001g0262a0001c0001t0001g0265others(11): Show | 14 | HG01099.hp1 HG01346.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.283+3544_283+3546d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | |||||
| chr11:43757639
|
C | CAAAA | 13 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(10): Show | 13 | HG00642.hp2 HG01496.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+3543_283+3546d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | |||||
| chr11:43757639
|
C | CAAAAA | 16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0123others(13): Show | 16 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+3542_283+3546d others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | |||||
| chr11:43757639
|
C | CAAAAAA | 15 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(12): Show | 15 | HG01106.hp1 HG01168.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+3541_283+3546d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | |||||
| chr11:43757639
|
C | CAAAAAAA | 9 | a0001c0001t0001g0004a0001c0001t0001g0213a0001c0001t0001g0216others(6): Show | 9 | HG00099.hp2 HG01167.hp2 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+3540_283+3546d others(9): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | |||||
| chr11:43757639
|
C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(7): Show | 10 | HG00140.hp1 HG02523.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+3539_283+3546d others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | |||||
| chr11:43757639
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283+3536_283+3546d others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | |||||
| chr11:43757639
|
CAAAAAAA others(3): Show |
C | 1 | a0003c0004t0001g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.283+3537_283+3546d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | |||||
| chr11:43757643
|
A | AACAAAAC others(5): Show |
1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+3523_283+3524i others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757643 | |||||
| chr11:43757646
|
A | AAAACAAA others(7): Show |
1 | a0001c0001t0003g0022 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.283+3528_283+3529i others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757646 | |||||
| chr11:43757648
|
A | C | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+3527A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757648 | ||||||
| chr11:43757651
|
A | AAAACAAA others(7): Show |
13 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(10): Show | 13 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+3533_283+3534i others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757651 | |||||
| chr11:43757651
|
A | C | 1 | a0001c0001t0003g0022 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.283+3530A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757651 | ||||||
| chr11:43757652
|
A | C | 1 | a0001c0001t0001g0092 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.283+3531A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757652 | ||||||
| chr11:43757653
|
A | C | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+3532A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757653 | ||||||
| chr11:43757656
|
A | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+3535A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757656 | ||||||
| chr11:43757658
|
A | C | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+3537A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757658 | ||||||
| chr11:43757661
|
A | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+3540A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757661 | ||||||
| chr11:43757716
|
C | CA | 52 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 52 | HG00099.hp2 HG00140.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.283+3603dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757716 | |||||
| chr11:43757717
|
A | AC | 21 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0215others(18): Show | 21 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.283+3596_283+3597i others(3): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757717 | ||||||
| chr11:43757968
|
G | A | 37 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(34): Show | 37 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.283+3847G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757968 | ||||||
| chr11:43758044
|
C | T | 37 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(34): Show | 37 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.283+3923C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758044 | ||||||
| chr11:43758322
|
G | A | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+4201G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758322 | ||||||
| chr11:43758470
|
C | G | 5 | a0002c0002t0002g0171a0002c0002t0002g0172a0002c0002t0002g0176others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+4349C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758470 | ||||||
| chr11:43758563
|
G | A | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+4442G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758563 | ||||||
| chr11:43758564
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.283+4443G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758564 | ||||||
| chr11:43758643
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.283+4522G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758643 | ||||||
| chr11:43758728
|
T | G | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0203others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+4607T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758728 | ||||||
| chr11:43758782
|
A | G | 1 | a0001c0003t0001g0242 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.283+4661A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758782 | ||||||
| chr11:43758845
|
A | G | 23 | a0002c0002t0002g0024a0002c0002t0002g0108a0002c0002t0002g0115others(20): Show | 23 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.283+4724A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758845 | ||||||
| chr11:43759003
|
C | A | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.283+4882C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759003 | ||||||
| chr11:43759087
|
A | G | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+4966A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759087 | ||||||
| chr11:43759423
|
A | G | 1 | a0002c0002t0002g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.283+5302A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759423 | ||||||
| chr11:43759516
|
A | G | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+5395A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759516 | ||||||
| chr11:43759525
|
A | T | 2 | a0002c0002t0002g0161a0002c0002t0002g0164 | 2 | HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.283+5404A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759525 | ||||||
| chr11:43759750
|
CAG | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+5632_283+5633d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43759750 | |||||
| chr11:43759886
|
C | T | 1 | a0001c0003t0003g0247 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.283+5765C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759886 | ||||||
| chr11:43759909
|
A | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0227 | 2 | HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.283+5788A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759909 | ||||||
| chr11:43759957
|
A | G | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+5836A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759957 | ||||||
| chr11:43759959
|
G | A | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+5838G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759959 | ||||||
| chr11:43760109
|
G | A | 3 | a0003c0004t0001g0231a0003c0004t0001g0244a0003c0004t0001g0252 | 3 | HG02647.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.283+5988G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760109 | ||||||
| chr11:43760201
|
T | A | 1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.283+6080T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760201 | ||||||
| chr11:43760231
|
G | A | 5 | a0002c0002t0002g0171a0002c0002t0002g0172a0002c0002t0002g0176others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+6110G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760231 | ||||||
| chr11:43760308
|
C | A | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+6187C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760308 | ||||||
| chr11:43760324
|
A | G | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+6203A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760324 | ||||||
| chr11:43760540
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.283+6419A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760540 | ||||||
| chr11:43760926
|
G | T | 1 | a0002c0002t0002g0139 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.283+6805G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760926 | ||||||
| chr11:43761078
|
T | TAGTC | 26 | a0001c0001t0001g0008a0001c0001t0001g0103a0001c0001t0001g0129others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.283+6958_283+6961d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43761078 | |||||
| chr11:43761151
|
T | C | 22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+7030T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761151 | ||||||
| chr11:43761174
|
T | C | 1 | a0001c0003t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.283+7053T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761174 | ||||||
| chr11:43761417
|
A | C | 8 | a0002c0002t0002g0003a0002c0002t0002g0144a0002c0002t0002g0145others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+7296A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761417 | ||||||
| chr11:43761485
|
A | C | 6 | a0002c0002t0002g0003a0002c0002t0002g0145a0002c0002t0002g0153others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+7364A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761485 | ||||||
| chr11:43761574
|
T | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+7453T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761574 | ||||||
| chr11:43761595
|
G | A | 1 | a0002c0002t0002g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.283+7474G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761595 | ||||||
| chr11:43761732
|
C | G | 39 | a0002c0002t0002g0003a0002c0002t0002g0024a0002c0002t0002g0108others(36): Show | 39 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.283+7611C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761732 | ||||||
| chr11:43761874
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+7753C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761874 | ||||||
| chr11:43761901
|
C | CTTTAAGT others(6): Show |
1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+7780_283+7781i others(15): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761901 | ||||||
| chr11:43761902
|
C | T | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+7781C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761902 | ||||||
| chr11:43762178
|
G | GA | 77 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(74): Show | 77 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.283+8065dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43762178 | |||||
| chr11:43762184
|
A | G | 22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+8063A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43762184 | ||||||
| chr11:43762429
|
T | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG01884.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+8308T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43762429 | ||||||
| chr11:43762454
|
C | T | 1 | a0001c0001t0003g0012 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.283+8333C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43762454 | ||||||
| chr11:43762718
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.283+8597C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43762718 | ||||||
| chr11:43762788
|
G | A | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+8667G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43762788 | ||||||
| chr11:43763001
|
A | T | 1 | a0001c0001t0001g0040 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.283+8880A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763001 | ||||||
| chr11:43763086
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.283+8965G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763086 | ||||||
| chr11:43763586
|
T | TTA | 59 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0051others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.283+9480_283+9481d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43763586 | |||||
| chr11:43763586
|
T | TTATA | 9 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+9478_283+9481d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43763586 | |||||
| chr11:43763588
|
A | G | 28 | a0002c0002t0002g0024a0002c0002t0002g0108a0002c0002t0002g0115others(25): Show | 28 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.283+9467A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763588 | ||||||
| chr11:43763611
|
T | TTA | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.283+9504_283+9505d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43763611 | |||||
| chr11:43763613
|
A | G | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+9492A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763613 | ||||||
| chr11:43763625
|
A | C | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+9504A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763625 | ||||||
| chr11:43763654
|
G | T | 228 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.283+9533G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763654 | ||||||
| chr11:43763656
|
G | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(39): Show | 42 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+9535G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763656 | ||||||
| chr11:43763658
|
G | T | 2 | a0001c0001t0001g0126a0002c0002t0009g0201 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+9537G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763658 | ||||||
| chr11:43763944
|
C | T | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+9823C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763944 | ||||||
| chr11:43763980
|
G | A | 7 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+9859G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763980 | ||||||
| chr11:43764117
|
T | A | 1 | a0001c0001t0001g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.283+9996T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764117 | ||||||
| chr11:43764118
|
A | T | 1 | a0001c0001t0001g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.283+9997A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764118 | ||||||
| chr11:43764169
|
C | G | 1 | a0002c0002t0002g0185 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.283+10048C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764169 | ||||||
| chr11:43764173
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.283+10052T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764173 | ||||||
| chr11:43764183
|
A | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+10062A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764183 | ||||||
| chr11:43764682
|
T | C | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+10561T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764682 | ||||||
| chr11:43764714
|
A | C | 1 | a0001c0001t0001g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.283+10593A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764714 | ||||||
| chr11:43764763
|
A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.283+10642A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764763 | ||||||
| chr11:43764841
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.283+10720C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764841 | ||||||
| chr11:43764880
|
G | A | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+10759G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764880 | ||||||
| chr11:43764929
|
C | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.283+10808C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764929 | ||||||
| chr11:43765004
|
G | GGATT | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+10883_283+1088 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765004 | ||||||
| chr11:43765011
|
A | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+10890A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765011 | ||||||
| chr11:43765563
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG03453.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.283+11442C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765563 | ||||||
| chr11:43765725
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0104 | 2 | HG01928.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.283+11604C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765725 | ||||||
| chr11:43765880
|
A | C | 17 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0003g0012others(14): Show | 17 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+11759A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765880 | ||||||
| chr11:43765958
|
C | T | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+11837C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765958 | ||||||
| chr11:43765971
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.283+11850G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765971 | ||||||
| chr11:43765986
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+11865C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765986 | ||||||
| chr11:43766015
|
C | T | 16 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0003g0012others(13): Show | 16 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(13): Show |
intron_variant | MODIFIER | c.283+11894C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766015 | ||||||
| chr11:43766105
|
G | A | 1 | a0002c0002t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.283+11984G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766105 | ||||||
| chr11:43766115
|
G | A | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.283+11994G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766115 | ||||||
| chr11:43766124
|
C | T | 19 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0266others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.283+12003C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766124 | ||||||
| chr11:43766154
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.283+12033G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766154 | ||||||
| chr11:43766225
|
C | CAATTAGT others(8): Show |
2 | a0001c0003t0003g0234a0001c0003t0003g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.283+12116_283+1213 others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43766225 | |||||
| chr11:43766258
|
G | T | 2 | a0001c0003t0003g0234a0001c0003t0003g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.283+12137G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766258 | ||||||
| chr11:43766284
|
C | T | 7 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+12163C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766284 | ||||||
| chr11:43766300
|
T | C | 21 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(18): Show | 21 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.283+12179T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766300 | ||||||
| chr11:43766390
|
A | G | 17 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0003g0012others(14): Show | 17 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+12269A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766390 | ||||||
| chr11:43766470
|
A | T | 2 | a0001c0003t0003g0234a0001c0003t0003g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.283+12349A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766470 | ||||||
| chr11:43766780
|
T | C | 113 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(110): Show | 113 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.283+12659T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766780 | ||||||
| chr11:43766811
|
G | T | 22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+12690G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766811 | ||||||
| chr11:43766909
|
C | T | 1 | a0001c0003t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.283+12788C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766909 | ||||||
| chr11:43767117
|
C | T | 17 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(14): Show | 17 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+12996C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43767117 | ||||||
| chr11:43767121
|
A | G | 7 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+13000A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43767121 | ||||||
| chr11:43767127
|
G | T | 1 | a0001c0001t0001g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.283+13006G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43767127 | ||||||
| chr11:43767204
|
T | TA | 77 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(74): Show | 77 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.283+13095dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43767204 | |||||
| chr11:43767214
|
A | AC | 15 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(12): Show | 15 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+13093_283+1309 others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43767214 | ||||||
| chr11:43767215
|
A | C | 13 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+13094A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43767215 | ||||||
| chr11:43767672
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+13551A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43767672 | ||||||
| chr11:43768100
|
T | G | 3 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195 | 3 | HG02559.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.283+13979T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768100 | ||||||
| chr11:43768122
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0069a0001c0001t0001g0091 | 3 | NA18612.hp1 NA18945.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.283+14001C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768122 | ||||||
| chr11:43768140
|
A | G | 1 | a0002c0002t0002g0128 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.283+14019A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768140 | ||||||
| chr11:43768288
|
G | A | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+14167G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768288 | ||||||
| chr11:43768373
|
G | C | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283+14252G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768373 | ||||||
| chr11:43768394
|
C | T | 17 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(14): Show | 17 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+14273C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768394 | ||||||
| chr11:43768440
|
T | C | 1 | a0002c0002t0002g0174 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.283+14319T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768440 | ||||||
| chr11:43768491
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.283+14370C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768491 | ||||||
| chr11:43768519
|
G | C | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.283+14398G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768519 | ||||||
| chr11:43768582
|
G | A | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02602.hp1 HG03834.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+14461G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768582 | ||||||
| chr11:43768633
|
T | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+14512T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768633 | ||||||
| chr11:43768652
|
T | C | 8 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(5): Show | 8 | HG02083.hp2 HG02698.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+14531T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768652 | ||||||
| chr11:43768656
|
A | T | 3 | a0002c0002t0004g0206a0002c0002t0004g0275a0002c0002t0009g0201 | 3 | HG02451.hp1 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.283+14535A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768656 | ||||||
| chr11:43768760
|
G | C | 1 | a0002c0002t0002g0181 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.283+14639G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768760 | ||||||
| chr11:43768764
|
G | T | 3 | a0001c0003t0001g0226a0001c0003t0001g0228a0001c0003t0001g0273 | 3 | HG00140.hp1 HG01167.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.283+14643G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768764 | ||||||
| chr11:43768772
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.283+14651G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768772 | ||||||
| chr11:43768784
|
G | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+14663G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768784 | ||||||
| chr11:43768815
|
C | T | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0203others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+14694C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768815 | ||||||
| chr11:43768825
|
CTGCTGAT others(17): Show |
C | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.283+14724_283+1474 others(28): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43768825 | |||||
| chr11:43769218
|
G | T | 22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+15097G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769218 | ||||||
| chr11:43769430
|
A | G | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+15309A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769430 | ||||||
| chr11:43769579
|
C | G | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+15458C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769579 | ||||||
| chr11:43769643
|
A | T | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+15522A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769643 | ||||||
| chr11:43769697
|
G | A | 1 | a0001c0001t0003g0023 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.283+15576G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769697 | ||||||
| chr11:43769716
|
C | T | 13 | a0002c0002t0002g0024a0002c0002t0002g0132a0002c0002t0002g0133others(10): Show | 13 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+15595C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769716 | ||||||
| chr11:43769907
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.283+15786A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769907 | ||||||
| chr11:43770259
|
C | T | 1 | a0002c0002t0002g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.283+16138C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770259 | ||||||
| chr11:43770315
|
G | A | 93 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(90): Show | 93 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.283+16194G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770315 | ||||||
| chr11:43770486
|
A | T | 1 | a0001c0001t0001g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.283+16365A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770486 | ||||||
| chr11:43770497
|
G | A | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+16376G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770497 | ||||||
| chr11:43770578
|
G | A | 37 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(34): Show | 37 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.283+16457G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770578 | ||||||
| chr11:43770588
|
C | T | 22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+16467C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770588 | ||||||
| chr11:43770598
|
T | C | 22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+16477T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770598 | ||||||
| chr11:43770608
|
C | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+16487C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770608 | ||||||
| chr11:43770630
|
G | A | 1 | a0002c0002t0002g0163 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.283+16509G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770630 | ||||||
| chr11:43771003
|
G | A | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283+16882G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43771003 | ||||||
| chr11:43771071
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.283+16950C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43771071 | ||||||
| chr11:43771311
|
C | G | 5 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(2): Show | 5 | NA18966.hp2 NA18971.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+17190C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43771311 | ||||||
| chr11:43771462
|
C | CT | 143 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0027others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.283+17363dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43771462 | |||||
| chr11:43771462
|
C | CTT | 22 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0031others(19): Show | 22 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+17362_283+1736 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43771462 | |||||
| chr11:43771462
|
CT | C | 16 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(13): Show | 16 | HG00609.hp2 HG00738.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+17363delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43771462 | |||||
| chr11:43771508
|
C | T | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+17387C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43771508 | ||||||
| chr11:43771611
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283+17490C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43771611 | ||||||
| chr11:43771800
|
A | G | 278 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.283+17679A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43771800 | ||||||
| chr11:43771819
|
A | G | 278 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.283+17698A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43771819 | ||||||
| chr11:43772023
|
CAT | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+17915_283+1791 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43772023 | |||||
| chr11:43772249
|
A | G | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.283+18128A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772249 | ||||||
| chr11:43772274
|
C | T | 1 | a0002c0002t0002g0057 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.283+18153C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772274 | ||||||
| chr11:43772533
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.283+18412T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772533 | ||||||
| chr11:43772813
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.283+18692A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772813 | ||||||
| chr11:43772829
|
A | G | 113 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(110): Show | 113 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.283+18708A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772829 | ||||||
| chr11:43772902
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.283+18781G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772902 | ||||||
| chr11:43772920
|
G | A | 23 | a0001c0001t0001g0008a0001c0001t0001g0187a0001c0001t0001g0209others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.283+18799G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772920 | ||||||
| chr11:43772974
|
G | A | 1 | a0002c0002t0002g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.283+18853G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772974 | ||||||
| chr11:43773042
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+18921T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773042 | ||||||
| chr11:43773043
|
G | A | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+18922G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773043 | ||||||
| chr11:43773067
|
C | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+18946C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773067 | ||||||
| chr11:43773340
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0009 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283+19219C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773340 | ||||||
| chr11:43773870
|
T | C | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.283+19749T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773870 | ||||||
| chr11:43773944
|
A | G | 1 | a0002c0002t0005g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+19823A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773944 | ||||||
| chr11:43773993
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.283+19872A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773993 | ||||||
| chr11:43774016
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283+19895T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774016 | ||||||
| chr11:43774128
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0086 | 2 | NA18952.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.283+20007C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774128 | ||||||
| chr11:43774218
|
A | AT | 7 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0203others(4): Show | 7 | HG01109.hp1 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+20111dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43774218 | |||||
| chr11:43774218
|
AT | A | 5 | a0001c0001t0003g0207a0001c0003t0003g0245a0003c0004t0001g0231others(2): Show | 5 | HG02647.hp2 HG03516.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+20111delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43774218 | |||||
| chr11:43774245
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.283+20124C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774245 | ||||||
| chr11:43774282
|
C | T | 43 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.283+20161C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774282 | ||||||
| chr11:43774389
|
G | A | 1 | a0002c0002t0010g0158 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.283+20268G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774389 | ||||||
| chr11:43774465
|
G | A | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+20344G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774465 | ||||||
| chr11:43774585
|
T | C | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+20464T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774585 | ||||||
| chr11:43774633
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.283+20512A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774633 | ||||||
| chr11:43774862
|
T | G | 22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+20741T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774862 | ||||||
| chr11:43775070
|
T | C | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.283+20949T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775070 | ||||||
| chr11:43775087
|
C | A | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0203others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+20966C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775087 | ||||||
| chr11:43775112
|
G | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+20991G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775112 | ||||||
| chr11:43775138
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.283+21017C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775138 | ||||||
| chr11:43775156
|
C | T | 40 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(37): Show | 40 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.283+21035C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775156 | ||||||
| chr11:43775184
|
C | A | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+21063C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775184 | ||||||
| chr11:43775204
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.283+21083G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775204 | ||||||
| chr11:43775249
|
C | A | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.283+21128C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775249 | ||||||
| chr11:43775285
|
C | CAT | 11 | a0002c0002t0002g0003a0002c0002t0002g0138a0002c0002t0002g0142others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+21171_283+2117 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43775285 | |||||
| chr11:43775318
|
G | T | 22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+21197G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775318 | ||||||
| chr11:43775341
|
A | G | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+21220A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775341 | ||||||
| chr11:43775367
|
T | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+21246T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775367 | ||||||
| chr11:43775484
|
AT | A | 52 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 52 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.283+21373delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43775484 | |||||
| chr11:43775714
|
C | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+21593C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775714 | ||||||
| chr11:43775715
|
G | A | 22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+21594G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775715 | ||||||
| chr11:43775742
|
A | G | 3 | a0002c0002t0002g0188a0002c0002t0002g0189a0002c0002t0002g0190 | 3 | HG00140.hp2 HG01167.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.283+21621A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775742 | ||||||
| chr11:43775748
|
T | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+21627T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775748 | ||||||
| chr11:43775758
|
C | G | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+21637C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775758 | ||||||
| chr11:43775764
|
C | T | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0203others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+21643C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775764 | ||||||
| chr11:43775817
|
T | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+21696T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775817 | ||||||
| chr11:43775877
|
C | A | 1 | a0002c0002t0002g0141 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.283+21756C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775877 | ||||||
| chr11:43775878
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+21757A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775878 | ||||||
| chr11:43775924
|
C | T | 66 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.283+21803C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775924 | ||||||
| chr11:43776007
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.283+21886G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776007 | ||||||
| chr11:43776119
|
A | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.283+21998A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776119 | ||||||
| chr11:43776291
|
G | A | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-22029G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776291 | ||||||
| chr11:43776313
|
G | T | 19 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0266others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.284-22007G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776313 | ||||||
| chr11:43776337
|
A | G | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-21983A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776337 | ||||||
| chr11:43776415
|
G | A | 1 | a0001c0003t0003g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.284-21905G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776415 | ||||||
| chr11:43776730
|
C | T | 1 | a0002c0002t0002g0150 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.284-21590C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776730 | ||||||
| chr11:43776773
|
G | A | 13 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-21547G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776773 | ||||||
| chr11:43776802
|
C | T | 2 | a0001c0003t0001g0241a0001c0003t0001g0274 | 2 | HG00642.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.284-21518C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776802 | ||||||
| chr11:43776910
|
A | G | 5 | a0002c0002t0002g0171a0002c0002t0002g0172a0002c0002t0002g0176others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-21410A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776910 | ||||||
| chr11:43776924
|
G | A | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.284-21396G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776924 | ||||||
| chr11:43776941
|
C | T | 7 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-21379C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776941 | ||||||
| chr11:43776942
|
T | A | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.284-21378T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776942 | ||||||
| chr11:43777010
|
G | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-21310G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777010 | ||||||
| chr11:43777138
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.284-21182T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777138 | ||||||
| chr11:43777182
|
T | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.284-21138T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777182 | ||||||
| chr11:43777183
|
A | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.284-21137A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777183 | ||||||
| chr11:43777185
|
AT | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.284-21133delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43777185 | |||||
| chr11:43777190
|
C | CAAGGCAA | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.284-21130_284-2112 others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777190 | ||||||
| chr11:43777280
|
G | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-21040G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777280 | ||||||
| chr11:43777322
|
A | G | 2 | a0001c0003t0001g0241a0001c0003t0001g0274 | 2 | HG00642.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.284-20998A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777322 | ||||||
| chr11:43777506
|
G | T | 1 | a0002c0002t0002g0115 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.284-20814G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777506 | ||||||
| chr11:43777553
|
C | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-20767C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777553 | ||||||
| chr11:43777573
|
G | C | 2 | a0001c0003t0001g0198a0001c0003t0001g0199 | 2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.284-20747G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777573 | ||||||
| chr11:43777576
|
C | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.284-20744C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777576 | ||||||
| chr11:43777684
|
C | T | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-20636C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777684 | ||||||
| chr11:43777725
|
A | G | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.284-20595A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777725 | ||||||
| chr11:43777748
|
G | A | 27 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(24): Show | 27 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.284-20572G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777748 | ||||||
| chr11:43777825
|
T | A | 1 | a0002c0002t0010g0158 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.284-20495T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777825 | ||||||
| chr11:43777825
|
T | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-20495T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777825 | ||||||
| chr11:43777895
|
T | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.284-20425T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777895 | ||||||
| chr11:43777905
|
G | A | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-20415G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777905 | ||||||
| chr11:43777929
|
A | G | 1 | a0002c0002t0002g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.284-20391A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777929 | ||||||
| chr11:43777964
|
G | A | 10 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(7): Show | 10 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-20356G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777964 | ||||||
| chr11:43778153
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.284-20167A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778153 | ||||||
| chr11:43778204
|
C | G | 1 | a0001c0001t0001g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.284-20116C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778204 | ||||||
| chr11:43778211
|
A | G | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.284-20109A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778211 | ||||||
| chr11:43778219
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.284-20101A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778219 | ||||||
| chr11:43778287
|
A | C | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-20033A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778287 | ||||||
| chr11:43778321
|
T | G | 1 | a0002c0002t0002g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.284-19999T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778321 | ||||||
| chr11:43778429
|
C | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-19891C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778429 | ||||||
| chr11:43778514
|
C | T | 22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.284-19806C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778514 | ||||||
| chr11:43778586
|
A | G | 15 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(12): Show | 15 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(12): Show |
intron_variant | MODIFIER | c.284-19734A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778586 | ||||||
| chr11:43778924
|
A | G | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-19396A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778924 | ||||||
| chr11:43778985
|
T | G | 2 | a0002c0002t0002g0039a0002c0002t0002g0157 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.284-19335T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778985 | ||||||
| chr11:43779076
|
T | G | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-19244T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779076 | ||||||
| chr11:43779118
|
A | G | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-19202A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779118 | ||||||
| chr11:43779139
|
G | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.284-19181G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779139 | ||||||
| chr11:43779141
|
A | T | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.284-19179A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779141 | ||||||
| chr11:43779154
|
C | T | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.284-19166C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779154 | ||||||
| chr11:43779217
|
G | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-19103G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779217 | ||||||
| chr11:43779218
|
A | G | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-19102A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779218 | ||||||
| chr11:43779457
|
A | G | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.284-18863A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779457 | ||||||
| chr11:43779511
|
A | T | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-18809A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779511 | ||||||
| chr11:43779519
|
G | T | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-18801G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779519 | ||||||
| chr11:43779552
|
C | A | 1 | a0002c0002t0002g0138 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.284-18768C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779552 | ||||||
| chr11:43779582
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.284-18738A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779582 | ||||||
| chr11:43779728
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.284-18592A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779728 | ||||||
| chr11:43779803
|
C | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-18517C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779803 | ||||||
| chr11:43779845
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.284-18475A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779845 | ||||||
| chr11:43779947
|
A | G | 2 | a0001c0003t0001g0198a0001c0003t0001g0199 | 2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.284-18373A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779947 | ||||||
| chr11:43779966
|
GGTAATCC others(1): Show |
G | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-18351_284-1834 others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43779966 | |||||
| chr11:43780082
|
C | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-18238C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43780082 | ||||||
| chr11:43780245
|
A | C | 1 | a0002c0002t0002g0115 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.284-18075A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43780245 | ||||||
| chr11:43780275
|
C | T | 22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.284-18045C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43780275 | ||||||
| chr11:43781160
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.284-17160A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781160 | ||||||
| chr11:43781316
|
C | A | 13 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(10): Show | 13 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-17004C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781316 | ||||||
| chr11:43781364
|
T | TG | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-16955dupG | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43781364 | |||||
| chr11:43781414
|
T | C | 1 | a0001c0003t0001g0242 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.284-16906T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781414 | ||||||
| chr11:43781563
|
A | G | 72 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(69): Show | 72 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.284-16757A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781563 | ||||||
| chr11:43781608
|
T | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-16712T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781608 | ||||||
| chr11:43781646
|
A | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-16674A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781646 | ||||||
| chr11:43781704
|
G | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.284-16616G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781704 | ||||||
| chr11:43781780
|
TTAAC | T | 2 | a0001c0003t0003g0234a0001c0003t0003g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.284-16536_284-1653 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43781780 | |||||
| chr11:43782007
|
G | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-16313G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782007 | ||||||
| chr11:43782308
|
G | A | 1 | a0002c0002t0002g0168 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.284-16012G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782308 | ||||||
| chr11:43782403
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.284-15917G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782403 | ||||||
| chr11:43782509
|
C | T | 1 | a0001c0001t0003g0015 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.284-15811C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782509 | ||||||
| chr11:43782599
|
C | T | 1 | a0001c0003t0001g0240 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.284-15721C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782599 | ||||||
| chr11:43782669
|
T | C | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-15651T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782669 | ||||||
| chr11:43782674
|
C | CA | 65 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(62): Show | 65 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.284-15630dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43782674 | |||||
| chr11:43782674
|
CA | C | 18 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.284-15630delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43782674 | |||||
| chr11:43782702
|
G | A | 1 | a0002c0002t0002g0109 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.284-15618G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782702 | ||||||
| chr11:43782769
|
A | G | 1 | a0002c0002t0002g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.284-15551A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782769 | ||||||
| chr11:43782876
|
A | G | 1 | a0002c0002t0004g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.284-15444A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782876 | ||||||
| chr11:43782880
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-15440G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782880 | ||||||
| chr11:43783030
|
A | G | 7 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-15290A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43783030 | ||||||
| chr11:43783130
|
A | G | 13 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-15190A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43783130 | ||||||
| chr11:43783331
|
G | A | 13 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-14989G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43783331 | ||||||
| chr11:43783397
|
C | CT | 15 | a0001c0001t0001g0008a0001c0001t0001g0059a0001c0001t0001g0060others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.284-14908dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43783397 | |||||
| chr11:43783604
|
C | G | 19 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0266others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.284-14716C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43783604 | ||||||
| chr11:43783614
|
TC | T | 13 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(10): Show | 13 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-14704delC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43783614 | |||||
| chr11:43783666
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.284-14654C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43783666 | ||||||
| chr11:43783797
|
T | TA | 23 | a0001c0001t0001g0008a0001c0001t0001g0187a0001c0001t0001g0209others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.284-14522dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43783797 | |||||
| chr11:43783955
|
C | G | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-14365C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43783955 | ||||||
| chr11:43784301
|
A | ATAT | 20 | a0001c0001t0001g0112a0001c0001t0001g0261a0001c0001t0001g0262others(17): Show | 20 | HG00408.hp2 HG01099.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.284-13975_284-1397 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | |||||
| chr11:43784301
|
A | ATATTAT | 3 | a0002c0002t0002g0153a0002c0002t0002g0156a0002c0002t0002g0178 | 3 | HG02630.hp2 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.284-13978_284-1397 others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | |||||
| chr11:43784301
|
ATAT | A | 46 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0036others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.284-13975_284-1397 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | |||||
| chr11:43784301
|
ATATTAT | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.284-13978_284-1397 others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | |||||
| chr11:43784301
|
ATATTATT others(2): Show |
A | 6 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0031others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-13981_284-1397 others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | |||||
| chr11:43784301
|
ATATTATT others(5): Show |
A | 1 | a0002c0002t0002g0116 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.284-13984_284-1397 others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | |||||
| chr11:43784301
|
ATATTATT others(11): Show |
A | 1 | a0001c0001t0001g0224 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.284-13990_284-1397 others(22): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | |||||
| chr11:43784432
|
T | A | 22 | a0002c0002t0002g0024a0002c0002t0002g0108a0002c0002t0002g0115others(19): Show | 22 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.284-13888T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43784432 | ||||||
| chr11:43784433
|
C | A | 22 | a0002c0002t0002g0024a0002c0002t0002g0108a0002c0002t0002g0115others(19): Show | 22 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.284-13887C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43784433 | ||||||
| chr11:43784726
|
G | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0087 | 2 | HG03239.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.284-13594G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43784726 | ||||||
| chr11:43784828
|
C | A | 2 | a0002c0002t0002g0039a0002c0002t0002g0157 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.284-13492C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43784828 | ||||||
| chr11:43784898
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.284-13422A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43784898 | ||||||
| chr11:43785096
|
GT | G | 170 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.284-13213delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43785096 | |||||
| chr11:43785097
|
T | G | 1 | a0002c0002t0002g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.284-13223T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785097 | ||||||
| chr11:43785187
|
G | A | 21 | a0001c0001t0001g0187a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-13133G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785187 | ||||||
| chr11:43785357
|
G | A | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-12963G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785357 | ||||||
| chr11:43785407
|
A | G | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.284-12913A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785407 | ||||||
| chr11:43785452
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.284-12868G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785452 | ||||||
| chr11:43785475
|
C | T | 4 | a0002c0002t0002g0163a0002c0002t0002g0181a0004c0005t0002g0010others(1): Show | 4 | HG00323.hp1 HG01099.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-12845C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785475 | ||||||
| chr11:43785723
|
T | C | 17 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(14): Show | 17 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.284-12597T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785723 | ||||||
| chr11:43785752
|
T | C | 1 | a0002c0002t0002g0164 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.284-12568T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785752 | ||||||
| chr11:43785842
|
T | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.284-12478T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785842 | ||||||
| chr11:43785971
|
A | G | 19 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0266others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.284-12349A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785971 | ||||||
| chr11:43786168
|
G | A | 9 | a0002c0002t0002g0003a0002c0002t0002g0144a0002c0002t0002g0145others(6): Show | 9 | HG00609.hp1 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-12152G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786168 | ||||||
| chr11:43786292
|
A | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-12028A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786292 | ||||||
| chr11:43786423
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.284-11897A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786423 | ||||||
| chr11:43786441
|
T | C | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-11879T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786441 | ||||||
| chr11:43786683
|
A | G | 4 | a0002c0002t0002g0001a0002c0002t0002g0026a0002c0002t0002g0057others(1): Show | 5 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-11637A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786683 | ||||||
| chr11:43786701
|
A | G | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-11619A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786701 | ||||||
| chr11:43786724
|
T | C | 33 | a0002c0002t0002g0001a0002c0002t0002g0026a0002c0002t0002g0039others(30): Show | 34 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.284-11596T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786724 | ||||||
| chr11:43786926
|
G | A | 1 | a0001c0003t0001g0274 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.284-11394G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786926 | ||||||
| chr11:43786954
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.284-11366T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786954 | ||||||
| chr11:43787013
|
C | T | 3 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0002g0195 | 3 | HG02559.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.284-11307C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787013 | ||||||
| chr11:43787322
|
A | G | 2 | a0001c0003t0001g0198a0001c0003t0001g0199 | 2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.284-10998A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787322 | ||||||
| chr11:43787361
|
G | T | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-10959G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787361 | ||||||
| chr11:43787489
|
C | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-10831C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787489 | ||||||
| chr11:43787502
|
C | T | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-10818C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787502 | ||||||
| chr11:43787736
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.284-10584C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787736 | ||||||
| chr11:43787738
|
G | GA | 92 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(89): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.284-10569dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43787738 | |||||
| chr11:43787746
|
A | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-10574A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787746 | ||||||
| chr11:43787749
|
A | T | 28 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(25): Show | 28 | HG00280.hp1 HG00609.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.284-10571A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787749 | ||||||
| chr11:43787752
|
T | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0045others(8): Show | 11 | HG00639.hp1 HG01070.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-10568T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787752 | ||||||
| chr11:43787857
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-10463C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787857 | ||||||
| chr11:43788045
|
A | T | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-10275A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788045 | ||||||
| chr11:43788136
|
CTT | C | 17 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(14): Show | 17 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.284-10180_284-1017 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43788136 | |||||
| chr11:43788283
|
C | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 52 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.284-10037C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788283 | ||||||
| chr11:43788445
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.284-9875C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788445 | ||||||
| chr11:43788554
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-9766C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788554 | ||||||
| chr11:43788612
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.284-9708T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788612 | ||||||
| chr11:43788639
|
A | G | 1 | a0002c0002t0002g0141 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.284-9681A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788639 | ||||||
| chr11:43788685
|
CA | C | 32 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.284-9611delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43788685 | |||||
| chr11:43788685
|
CAAAAA | C | 85 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(82): Show | 85 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.284-9615_284-9611d others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43788685 | |||||
| chr11:43788685
|
CAAAAAAA | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-9617_284-9611d others(9): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43788685 | |||||
| chr11:43788709
|
A | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0112 | 3 | HG02300.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.284-9611A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788709 | ||||||
| chr11:43788794
|
A | T | 1 | a0001c0003t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.284-9526A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788794 | ||||||
| chr11:43788909
|
T | C | 112 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.284-9411T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788909 | ||||||
| chr11:43788949
|
A | G | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.284-9371A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788949 | ||||||
| chr11:43789059
|
T | C | 1 | a0001c0003t0001g0242 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.284-9261T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789059 | ||||||
| chr11:43789063
|
G | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-9257G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789063 | ||||||
| chr11:43789067
|
G | C | 3 | a0003c0004t0001g0231a0003c0004t0001g0244a0003c0004t0001g0252 | 3 | HG02647.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.284-9253G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789067 | ||||||
| chr11:43789527
|
C | A | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-8793C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789527 | ||||||
| chr11:43789669
|
T | C | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-8651T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789669 | ||||||
| chr11:43789683
|
T | A | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-8637T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789683 | ||||||
| chr11:43789775
|
C | T | 3 | a0002c0002t0002g0181a0004c0005t0002g0010a0004c0005t0002g0011 | 3 | HG01099.hp2 HG01106.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.284-8545C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789775 | ||||||
| chr11:43789917
|
G | A | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-8403G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789917 | ||||||
| chr11:43789932
|
A | G | 39 | a0002c0002t0002g0003a0002c0002t0002g0024a0002c0002t0002g0108others(36): Show | 39 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.284-8388A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789932 | ||||||
| chr11:43790093
|
C | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-8227C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43790093 | ||||||
| chr11:43790512
|
G | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0048 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.284-7808G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43790512 | ||||||
| chr11:43790681
|
G | A | 21 | a0001c0001t0001g0187a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-7639G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43790681 | ||||||
| chr11:43791014
|
TA | T | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-7297delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43791014 | |||||
| chr11:43791015
|
A | T | 1 | a0001c0003t0001g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.284-7305A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43791015 | ||||||
| chr11:43791267
|
C | T | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0203others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-7053C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43791267 | ||||||
| chr11:43791348
|
G | A | 278 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.284-6972G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43791348 | ||||||
| chr11:43791489
|
A | G | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-6831A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43791489 | ||||||
| chr11:43791647
|
G | A | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-6673G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43791647 | ||||||
| chr11:43791676
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.284-6644G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43791676 | ||||||
| chr11:43791838
|
A | G | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-6482A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43791838 | ||||||
| chr11:43792000
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0009 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.284-6320G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792000 | ||||||
| chr11:43792134
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-6186G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792134 | ||||||
| chr11:43792171
|
G | A | 1 | a0001c0001t0003g0012 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.284-6149G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792171 | ||||||
| chr11:43792226
|
T | G | 222 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.284-6094T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792226 | ||||||
| chr11:43792262
|
G | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0104 | 2 | HG01928.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.284-6058G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792262 | ||||||
| chr11:43792525
|
A | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0009 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.284-5795A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792525 | ||||||
| chr11:43792644
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-5676A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792644 | ||||||
| chr11:43792682
|
C | CT | 64 | a0001c0001t0001g0031a0001c0001t0001g0099a0001c0001t0001g0110others(61): Show | 64 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.284-5616dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43792682 | |||||
| chr11:43792682
|
C | CTT | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(31): Show | 34 | HG00140.hp1 HG01167.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.284-5617_284-5616d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43792682 | |||||
| chr11:43792682
|
C | CTTT | 22 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0215others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.284-5618_284-5616d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43792682 | |||||
| chr11:43792682
|
CT | C | 35 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0059others(32): Show | 35 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.284-5616delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43792682 | |||||
| chr11:43792740
|
C | A | 1 | a0001c0001t0001g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.284-5580C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792740 | ||||||
| chr11:43793020
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0069 | 2 | NA18945.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.284-5300G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793020 | ||||||
| chr11:43793104
|
C | T | 1 | a0002c0002t0002g0185 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.284-5216C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793104 | ||||||
| chr11:43793572
|
A | G | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.284-4748A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793572 | ||||||
| chr11:43793654
|
G | A | 1 | a0002c0002t0002g0277 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.284-4666G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793654 | ||||||
| chr11:43793707
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-4613G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793707 | ||||||
| chr11:43793708
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-4612G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793708 | ||||||
| chr11:43793710
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-4610T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793710 | ||||||
| chr11:43793711
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-4609C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793711 | ||||||
| chr11:43793715
|
T | G | 1 | a0001c0001t0001g0085 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-4605T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793715 | ||||||
| chr11:43793716
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-4604C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793716 | ||||||
| chr11:43793867
|
C | T | 13 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-4453C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793867 | ||||||
| chr11:43794050
|
A | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.284-4270A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794050 | ||||||
| chr11:43794167
|
A | G | 71 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(68): Show | 71 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.284-4153A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794167 | ||||||
| chr11:43794256
|
A | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.284-4064A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794256 | ||||||
| chr11:43794317
|
A | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG03453.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.284-4003A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794317 | ||||||
| chr11:43794513
|
C | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-3807C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794513 | ||||||
| chr11:43794650
|
C | T | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.284-3670C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794650 | ||||||
| chr11:43794845
|
G | A | 2 | a0002c0002t0002g0193a0002c0002t0002g0195 | 2 | HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.284-3475G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794845 | ||||||
| chr11:43795024
|
G | GA | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.284-3288dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43795024 | |||||
| chr11:43795059
|
A | G | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-3261A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795059 | ||||||
| chr11:43795091
|
C | T | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.284-3229C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795091 | ||||||
| chr11:43795575
|
C | T | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.284-2745C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795575 | ||||||
| chr11:43795634
|
C | T | 21 | a0001c0001t0001g0187a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-2686C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795634 | ||||||
| chr11:43795635
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-2685G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795635 | ||||||
| chr11:43795770
|
C | G | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.284-2550C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795770 | ||||||
| chr11:43795812
|
A | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.284-2508A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795812 | ||||||
| chr11:43795820
|
G | A | 4 | a0002c0002t0002g0253a0002c0002t0002g0254a0002c0002t0002g0255others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-2500G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795820 | ||||||
| chr11:43795913
|
G | C | 1 | a0002c0002t0002g0109 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.284-2407G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795913 | ||||||
| chr11:43796044
|
C | G | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.284-2276C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796044 | ||||||
| chr11:43796148
|
A | G | 1 | a0002c0002t0002g0101 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.284-2172A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796148 | ||||||
| chr11:43796161
|
G | A | 1 | a0002c0002t0002g0132 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.284-2159G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796161 | ||||||
| chr11:43796180
|
C | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.284-2140C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796180 | ||||||
| chr11:43796232
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0197 | 2 | NA18943.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.284-2088A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796232 | ||||||
| chr11:43796276
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.284-2044G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796276 | ||||||
| chr11:43796332
|
T | G | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.284-1988T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796332 | ||||||
| chr11:43796505
|
T | C | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.284-1815T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796505 | ||||||
| chr11:43796844
|
C | CT | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.284-1467dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43796844 | |||||
| chr11:43796976
|
T | C | 4 | a0002c0002t0002g0171a0002c0002t0002g0172a0002c0002t0002g0178others(1): Show | 4 | HG02723.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-1344T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796976 | ||||||
| chr11:43797224
|
G | A | 1 | a0001c0003t0001g0238 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.284-1096G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43797224 | ||||||
| chr11:43797273
|
C | G | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-1047C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43797273 | ||||||
| chr11:43797414
|
C | T | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.284-906C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43797414 | ||||||
| chr11:43797814
|
T | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0049others(1): Show | 4 | HG02155.hp1 HG03704.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-506T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43797814 | ||||||
| chr11:43797887
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-433G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43797887 | ||||||
| chr11:43797957
|
A | G | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0271 | 3 | HG02451.hp2 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.284-363A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43797957 | ||||||
| chr11:43798064
|
A | G | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.284-256A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43798064 | ||||||
| chr11:43798453
|
G | GTATTTA | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+27_391+28insAT others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43798453 | |||||
| chr11:43798456
|
C | A | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+29C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43798456 | ||||||
| chr11:43798658
|
C | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.391+231C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43798658 | ||||||
| chr11:43798698
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG01261.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+271A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43798698 | ||||||
| chr11:43798762
|
G | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+335G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43798762 | ||||||
| chr11:43798926
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+499T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43798926 | ||||||
| chr11:43798974
|
C | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+547C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43798974 | ||||||
| chr11:43799169
|
A | G | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.391+742A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43799169 | ||||||
| chr11:43799279
|
A | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0227 | 2 | HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.391+852A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43799279 | ||||||
| chr11:43799454
|
G | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+1027G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43799454 | ||||||
| chr11:43799708
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.391+1281A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43799708 | ||||||
| chr11:43799805
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+1378C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43799805 | ||||||
| chr11:43799857
|
C | T | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.391+1430C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43799857 | ||||||
| chr11:43800048
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.391+1621C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43800048 | ||||||
| chr11:43800204
|
A | C | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.391+1777A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43800204 | ||||||
| chr11:43800438
|
A | C | 7 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.391+2011A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43800438 | ||||||
| chr11:43800509
|
TG | T | 71 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.391+2083delG | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43800509 | ||||||
| chr11:43800909
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.391+2482C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43800909 | ||||||
| chr11:43800959
|
C | T | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.391+2532C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43800959 | ||||||
| chr11:43801038
|
C | T | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.391+2611C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43801038 | ||||||
| chr11:43801087
|
C | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+2660C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43801087 | ||||||
| chr11:43801092
|
T | C | 11 | a0002c0002t0002g0003a0002c0002t0002g0138a0002c0002t0002g0142others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.391+2665T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43801092 | ||||||
| chr11:43801144
|
G | GA | 7 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(4): Show | 7 | HG01109.hp1 HG01496.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.391+2727dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801144 | |||||
| chr11:43801144
|
GA | G | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+2727delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801144 | |||||
| chr11:43801207
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+2780T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43801207 | ||||||
| chr11:43801208
|
G | A | 72 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(69): Show | 72 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.391+2781G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43801208 | ||||||
| chr11:43801335
|
A | G | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.391+2908A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43801335 | ||||||
| chr11:43801593
|
GAGATATA others(33): Show |
G | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.391+3168_391+3207d others(42): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801593 | |||||
| chr11:43801595
|
G | GAT | 6 | a0001c0001t0003g0066a0002c0002t0002g0171a0002c0002t0002g0174others(3): Show | 6 | HG00738.hp1 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.391+3203_391+3204d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | |||||
| chr11:43801595
|
G | GATAT | 11 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0017others(8): Show | 11 | HG00280.hp2 HG01099.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.391+3201_391+3204d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | |||||
| chr11:43801595
|
G | GATATAT | 8 | a0001c0001t0003g0013a0001c0001t0003g0015a0001c0001t0003g0021others(5): Show | 8 | NA18944.hp2 NA18948.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.391+3199_391+3204d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | |||||
| chr11:43801595
|
G | GATATATA others(1): Show |
8 | a0001c0001t0003g0012a0001c0001t0003g0019a0002c0002t0002g0108others(5): Show | 8 | HG00423.hp1 HG02080.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.391+3197_391+3204d others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | |||||
| chr11:43801595
|
G | GATATATA others(3): Show |
2 | a0002c0002t0002g0024a0005c0006t0012g0020 | 2 | HG00609.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.391+3195_391+3204d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | |||||
| chr11:43801595
|
G | GATATATA others(5): Show |
2 | a0001c0001t0003g0093a0002c0002t0002g0255 | 2 | HG01891.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.391+3193_391+3204d others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | |||||
| chr11:43801595
|
G | GATATATA others(3): Show |
1 | a0002c0002t0002g0132 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.391+3176_391+3177i others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | |||||
| chr11:43801595
|
GAT | G | 7 | a0002c0002t0002g0148a0002c0002t0002g0149a0002c0002t0002g0157others(4): Show | 7 | HG02155.hp2 HG02698.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.391+3203_391+3204d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | |||||
| chr11:43801595
|
GATAT | G | 30 | a0002c0002t0002g0001a0002c0002t0002g0026a0002c0002t0002g0039others(27): Show | 31 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.391+3201_391+3204d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | |||||
| chr11:43801595
|
GATATAT | G | 14 | a0002c0002t0002g0057a0002c0002t0002g0116a0002c0002t0002g0117others(11): Show | 14 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.391+3199_391+3204d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | |||||
| chr11:43801595
|
GATATATA others(3): Show |
G | 2 | a0002c0002t0002g0138a0002c0002t0002g0154 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.391+3195_391+3204d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | |||||
| chr11:43801595
|
GATATATA others(5): Show |
G | 12 | a0002c0002t0002g0003a0002c0002t0002g0115a0002c0002t0002g0127others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.391+3193_391+3204d others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | |||||
| chr11:43801977
|
AT | A | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.391+3562delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801977 | |||||
| chr11:43802048
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.391+3621C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802048 | ||||||
| chr11:43802059
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.391+3632C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802059 | ||||||
| chr11:43802208
|
G | A | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+3781G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802208 | ||||||
| chr11:43802413
|
A | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+3986A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802413 | ||||||
| chr11:43802757
|
G | A | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.391+4330G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802757 | ||||||
| chr11:43802811
|
T | C | 1 | a0001c0003t0001g0243 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.391+4384T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802811 | ||||||
| chr11:43802823
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.391+4396G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802823 | ||||||
| chr11:43803083
|
A | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+4656A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803083 | ||||||
| chr11:43803228
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.391+4801G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803228 | ||||||
| chr11:43803488
|
C | T | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.391+5061C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803488 | ||||||
| chr11:43803596
|
T | C | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.391+5169T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803596 | ||||||
| chr11:43803722
|
A | G | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+5295A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803722 | ||||||
| chr11:43803816
|
G | A | 72 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(69): Show | 72 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.391+5389G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803816 | ||||||
| chr11:43803931
|
C | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+5504C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803931 | ||||||
| chr11:43804045
|
G | A | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.391+5618G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43804045 | ||||||
| chr11:43804260
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.391+5833G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43804260 | ||||||
| chr11:43804373
|
C | T | 13 | a0002c0002t0002g0024a0002c0002t0002g0132a0002c0002t0002g0133others(10): Show | 13 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.391+5946C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43804373 | ||||||
| chr11:43804443
|
G | A | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.391+6016G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43804443 | ||||||
| chr11:43805030
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0009 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.391+6603A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805030 | ||||||
| chr11:43805104
|
G | A | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.391+6677G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805104 | ||||||
| chr11:43805179
|
A | G | 1 | a0002c0002t0002g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.391+6752A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805179 | ||||||
| chr11:43805249
|
G | GTAAATAC others(3): Show |
18 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.391+6827_391+6836d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43805249 | |||||
| chr11:43805321
|
T | A | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+6894T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805321 | ||||||
| chr11:43805505
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.391+7078A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805505 | ||||||
| chr11:43805542
|
G | A | 3 | a0001c0003t0001g0241a0001c0003t0001g0242a0001c0003t0001g0274 | 3 | HG00642.hp2 HG02735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.391+7115G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805542 | ||||||
| chr11:43805622
|
T | C | 1 | a0002c0002t0002g0163 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.391+7195T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805622 | ||||||
| chr11:43805701
|
C | T | 2 | a0002c0002t0002g0039a0002c0002t0002g0157 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.391+7274C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805701 | ||||||
| chr11:43805724
|
T | G | 8 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(5): Show | 8 | HG02083.hp2 HG02698.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.391+7297T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805724 | ||||||
| chr11:43805887
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.391+7460G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805887 | ||||||
| chr11:43805961
|
G | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.391+7534G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805961 | ||||||
| chr11:43806095
|
C | T | 1 | a0002c0002t0006g0107 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.391+7668C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806095 | ||||||
| chr11:43806384
|
A | C | 13 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.391+7957A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806384 | ||||||
| chr11:43806460
|
G | A | 1 | a0002c0002t0002g0163 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.391+8033G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806460 | ||||||
| chr11:43806495
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.391+8068A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806495 | ||||||
| chr11:43806513
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.391+8086A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806513 | ||||||
| chr11:43806543
|
A | C | 21 | a0001c0001t0001g0187a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.391+8116A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806543 | ||||||
| chr11:43806544
|
A | G | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.391+8117A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806544 | ||||||
| chr11:43806785
|
A | C | 14 | a0002c0002t0002g0039a0002c0002t0002g0128a0002c0002t0002g0140others(11): Show | 14 | HG00140.hp2 HG00735.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.391+8358A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806785 | ||||||
| chr11:43806840
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.391+8413C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806840 | ||||||
| chr11:43807009
|
A | ACACTGTT others(2): Show |
183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.392-8425_392-8417d others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43807009 | |||||
| chr11:43807209
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.392-8228G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43807209 | ||||||
| chr11:43807262
|
T | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0009 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.392-8175T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43807262 | ||||||
| chr11:43807459
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.392-7978G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43807459 | ||||||
| chr11:43807987
|
A | G | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.392-7450A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43807987 | ||||||
| chr11:43808058
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.392-7379C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43808058 | ||||||
| chr11:43808290
|
AT | A | 128 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(125): Show | 128 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.392-7131delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43808290 | |||||
| chr11:43808931
|
G | T | 2 | a0001c0003t0003g0234a0001c0003t0003g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.392-6506G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43808931 | ||||||
| chr11:43809060
|
A | G | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.392-6377A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809060 | ||||||
| chr11:43809248
|
G | A | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.392-6189G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809248 | ||||||
| chr11:43809345
|
T | C | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.392-6092T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809345 | ||||||
| chr11:43809521
|
A | T | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.392-5916A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809521 | ||||||
| chr11:43809593
|
C | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.392-5844C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809593 | ||||||
| chr11:43809628
|
G | T | 12 | a0002c0002t0002g0132a0002c0002t0002g0133a0002c0002t0002g0134others(9): Show | 12 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.392-5809G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809628 | ||||||
| chr11:43809636
|
T | C | 1 | a0002c0002t0002g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.392-5801T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809636 | ||||||
| chr11:43809684
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.392-5753G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809684 | ||||||
| chr11:43809772
|
C | T | 1 | a0002c0002t0002g0141 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.392-5665C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809772 | ||||||
| chr11:43809961
|
G | A | 18 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.392-5476G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809961 | ||||||
| chr11:43810002
|
G | A | 77 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(74): Show | 77 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.392-5435G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810002 | ||||||
| chr11:43810022
|
T | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0126 | 3 | HG01884.hp2 HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.392-5415T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810022 | ||||||
| chr11:43810226
|
A | G | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.392-5211A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810226 | ||||||
| chr11:43810312
|
CT | C | 13 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(10): Show | 13 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.392-5118delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810312 | |||||
| chr11:43810367
|
T | TTA | 3 | a0002c0002t0002g0131a0002c0002t0002g0136a0002c0002t0002g0185 | 3 | NA18943.hp2 NA18953.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.392-5035_392-5034d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
T | TTATA | 6 | a0002c0002t0002g0137a0002c0002t0002g0140a0002c0002t0002g0141others(3): Show | 6 | HG00140.hp2 HG01123.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-5037_392-5034d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
T | TTATATA | 8 | a0002c0002t0002g0056a0002c0002t0002g0064a0002c0002t0002g0109others(5): Show | 8 | HG00323.hp1 HG01070.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.392-5039_392-5034d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
T | TTATATAT others(1): Show |
11 | a0002c0002t0002g0001a0002c0002t0002g0026a0002c0002t0002g0039others(8): Show | 12 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.392-5041_392-5034d others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
T | TTATATAT others(3): Show |
1 | a0002c0002t0002g0147 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.392-5043_392-5034d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
T | TTATATAT others(5): Show |
5 | a0002c0002t0002g0101a0002c0002t0002g0127a0002c0002t0002g0154others(2): Show | 5 | HG01884.hp1 HG01975.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-5045_392-5034d others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
T | TTATATAT others(7): Show |
2 | a0002c0002t0002g0170a0002c0002t0002g0183 | 2 | NA18964.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.392-5047_392-5034d others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
T | TTATATAT others(9): Show |
5 | a0002c0002t0002g0115a0002c0002t0002g0139a0002c0002t0002g0153others(2): Show | 5 | HG00639.hp1 HG01109.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-5049_392-5034d others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
T | TTATATAT others(11): Show |
4 | a0002c0002t0002g0135a0002c0002t0002g0138a0002c0002t0002g0144others(1): Show | 4 | HG02257.hp2 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-5051_392-5034d others(20): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
T | TTATATAT others(13): Show |
6 | a0002c0002t0002g0003a0002c0002t0002g0024a0002c0002t0002g0156others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-5053_392-5034d others(22): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
T | TTATATAT others(15): Show |
7 | a0002c0002t0002g0108a0002c0002t0002g0133a0002c0002t0002g0134others(4): Show | 7 | HG00423.hp1 HG02723.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-5055_392-5034d others(24): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
T | TTATATAT others(17): Show |
2 | a0002c0002t0002g0142a0002c0002t0002g0175 | 2 | HG02976.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.392-5057_392-5034d others(26): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
T | TTATATAT others(19): Show |
1 | a0002c0002t0002g0192 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.392-5059_392-5034d others(28): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
TTA | T | 3 | a0002c0002t0002g0194a0002c0002t0002g0229a0002c0002t0002g0276 | 3 | HG02559.hp1 HG02723.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.392-5035_392-5034d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
TTATATA | T | 6 | a0002c0002t0002g0193a0002c0002t0002g0195a0002c0002t0002g0253others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-5039_392-5034d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
TTATATAT others(1): Show |
T | 8 | a0002c0002t0002g0132a0002c0002t0002g0165a0002c0002t0002g0166others(5): Show | 8 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.392-5041_392-5034d others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
TTATATAT others(3): Show |
T | 3 | a0001c0001t0001g0005a0001c0001t0001g0009a0002c0002t0002g0151 | 3 | HG02257.hp1 HG04184.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.392-5043_392-5034d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
TTATATAT others(5): Show |
T | 1 | a0001c0001t0001g0071 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.392-5045_392-5034d others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810367
|
TTATATAT others(7): Show |
T | 93 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(90): Show | 93 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.392-5047_392-5034d others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | |||||
| chr11:43810369
|
A | T | 86 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.392-5068A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810369 | ||||||
| chr11:43810379
|
A | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0009 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.392-5058A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810379 | ||||||
| chr11:43810381
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.392-5056A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810381 | ||||||
| chr11:43810383
|
A | T | 91 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(88): Show | 91 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.392-5054A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810383 | ||||||
| chr11:43810390
|
TATATATA others(7): Show |
T | 16 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.392-5045_392-5032d others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810390 | |||||
| chr11:43810392
|
TATATATA others(5): Show |
T | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.392-5043_392-5032d others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810392 | |||||
| chr11:43810394
|
TATATATA others(3): Show |
T | 25 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(22): Show | 25 | HG00280.hp1 HG00609.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.392-5041_392-5032d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810394 | |||||
| chr11:43810396
|
TATATATA others(1): Show |
T | 4 | a0001c0001t0001g0008a0001c0001t0001g0227a0001c0001t0001g0266others(1): Show | 4 | HG01261.hp2 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-5039_392-5032d others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810396 | |||||
| chr11:43810398
|
TATATAA | T | 13 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0267others(10): Show | 13 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.392-5037_392-5032d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810398 | |||||
| chr11:43810402
|
T | A | 2 | a0002c0002t0002g0193a0002c0002t0002g0195 | 2 | HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.392-5035T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810402 | ||||||
| chr11:43810403
|
A | ATATATAT others(8): Show |
2 | a0002c0002t0002g0172a0002c0002t0002g0263 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.392-5034_392-5033i others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810403 | ||||||
| chr11:43810404
|
A | T | 1 | a0003c0004t0001g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.392-5033A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810404 | ||||||
| chr11:43810420
|
C | T | 17 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(14): Show | 17 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.392-5017C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810420 | ||||||
| chr11:43810464
|
G | C | 3 | a0003c0004t0001g0231a0003c0004t0001g0244a0003c0004t0001g0252 | 3 | HG02647.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.392-4973G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810464 | ||||||
| chr11:43810613
|
T | C | 18 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.392-4824T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810613 | ||||||
| chr11:43810746
|
G | A | 19 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0266others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.392-4691G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810746 | ||||||
| chr11:43810951
|
G | A | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-4486G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810951 | ||||||
| chr11:43810955
|
G | A | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.392-4482G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810955 | ||||||
| chr11:43811051
|
A | G | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.392-4386A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43811051 | ||||||
| chr11:43811184
|
G | A | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.392-4253G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43811184 | ||||||
| chr11:43811967
|
C | T | 1 | a0002c0002t0010g0158 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.392-3470C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43811967 | ||||||
| chr11:43812174
|
A | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-3263A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812174 | ||||||
| chr11:43812181
|
C | T | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.392-3256C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812181 | ||||||
| chr11:43812300
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0045 | 2 | HG02004.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.392-3137T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812300 | ||||||
| chr11:43812366
|
G | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.392-3071G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812366 | ||||||
| chr11:43812386
|
T | A | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.392-3051T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812386 | ||||||
| chr11:43812478
|
G | A | 1 | a0002c0002t0002g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.392-2959G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812478 | ||||||
| chr11:43812507
|
G | C | 1 | a0001c0003t0003g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.392-2930G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812507 | ||||||
| chr11:43812901
|
G | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.392-2536G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812901 | ||||||
| chr11:43813290
|
T | A | 1 | a0001c0001t0001g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.392-2147T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43813290 | ||||||
| chr11:43813291
|
A | T | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.392-2146A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43813291 | ||||||
| chr11:43813537
|
TTTTG | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.392-1896_392-1893d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43813537 | |||||
| chr11:43813761
|
T | G | 1 | a0002c0002t0002g0162 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.392-1676T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43813761 | ||||||
| chr11:43813936
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.392-1501T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43813936 | ||||||
| chr11:43813957
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.392-1480C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43813957 | ||||||
| chr11:43814019
|
G | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0051 | 3 | HG03704.hp1 HG03834.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.392-1418G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814019 | ||||||
| chr11:43814164
|
AT | A | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.392-1262delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43814164 | |||||
| chr11:43814197
|
G | C | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.392-1240G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814197 | ||||||
| chr11:43814207
|
G | A | 1 | a0002c0002t0002g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.392-1230G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814207 | ||||||
| chr11:43814289
|
G | A | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0203others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-1148G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814289 | ||||||
| chr11:43814392
|
A | G | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.392-1045A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814392 | ||||||
| chr11:43814455
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.392-982T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814455 | ||||||
| chr11:43814521
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.392-916G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814521 | ||||||
| chr11:43814705
|
T | C | 3 | a0001c0003t0001g0226a0001c0003t0001g0228a0001c0003t0001g0273 | 3 | HG00140.hp1 HG01167.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.392-732T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814705 | ||||||
| chr11:43814789
|
A | G | 2 | a0004c0005t0002g0010a0004c0005t0002g0011 | 2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.392-648A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814789 | ||||||
| chr11:43814821
|
T | C | 1 | a0001c0003t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.392-616T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814821 | ||||||
| chr11:43814906
|
C | T | 7 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-531C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814906 | ||||||
| chr11:43815046
|
T | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.392-391T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43815046 | ||||||
| chr11:43815062
|
C | T | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.392-375C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43815062 | ||||||
| chr11:43815103
|
G | T | 2 | a0001c0003t0003g0234a0001c0003t0003g0235 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.392-334G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43815103 | ||||||
| chr11:43815162
|
T | C | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.392-275T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43815162 | ||||||
| chr11:43815282
|
T | C | 7 | a0002c0002t0002g0165a0002c0002t0002g0166a0002c0002t0002g0167others(4): Show | 7 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-155T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43815282 | ||||||
| chr11:43815523
|
A | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+22A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43815523 | ||||||
| chr11:43815623
|
T | C | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.456+122T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43815623 | ||||||
| chr11:43815696
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0048 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.456+195T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43815696 | ||||||
| chr11:43815804
|
A | G | 7 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(4): Show | 7 | HG01109.hp1 HG01496.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.456+303A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43815804 | ||||||
| chr11:43815848
|
A | C | 1 | a0001c0001t0001g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.456+347A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43815848 | ||||||
| chr11:43815935
|
G | A | 1 | a0002c0002t0004g0275 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457-412G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43815935 | ||||||
| chr11:43816001
|
A | G | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.457-346A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43816001 | ||||||
| chr11:43816039
|
A | G | 1 | a0002c0002t0002g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.457-308A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43816039 | ||||||
| chr11:43816466
|
T | C | 1 | a0002c0002t0002g0108 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.501+75T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43816466 | ||||||
| chr11:43816574
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0078 | 2 | NA18941.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.501+183C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43816574 | ||||||
| chr11:43816585
|
T | C | 13 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.501+194T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43816585 | ||||||
| chr11:43816767
|
T | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.501+376T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43816767 | ||||||
| chr11:43816791
|
C | T | 5 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(2): Show | 5 | NA18966.hp2 NA18971.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+400C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43816791 | ||||||
| chr11:43816890
|
G | A | 28 | a0002c0002t0002g0024a0002c0002t0002g0108a0002c0002t0002g0115others(25): Show | 28 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.501+499G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43816890 | ||||||
| chr11:43816980
|
A | ATATATC | 4 | a0002c0002t0002g0153a0002c0002t0002g0162a0002c0002t0002g0173others(1): Show | 4 | HG02622.hp1 HG02717.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+649_501+654dup others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | |||||
| chr11:43816980
|
A | ATATATCT others(5): Show |
1 | a0002c0002t0002g0156 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.501+643_501+654dup others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | |||||
| chr11:43816980
|
ATATATC | A | 41 | a0002c0002t0002g0001a0002c0002t0002g0026a0002c0002t0002g0055others(38): Show | 42 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.501+649_501+654del others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | |||||
| chr11:43816980
|
ATATATCT others(5): Show |
A | 27 | a0002c0002t0002g0039a0002c0002t0002g0064a0002c0002t0002g0109others(24): Show | 27 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.501+643_501+654del others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | |||||
| chr11:43816980
|
ATATATCT others(11): Show |
A | 8 | a0001c0001t0003g0012a0001c0001t0003g0014a0001c0001t0003g0016others(5): Show | 8 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.501+637_501+654del others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | |||||
| chr11:43816980
|
ATATATCT others(17): Show |
A | 2 | a0001c0001t0003g0022a0002c0002t0008g0002 | 2 | HG00280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.501+631_501+654del others(24): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | |||||
| chr11:43816980
|
ATATATCT others(23): Show |
A | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.501+625_501+654del others(30): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | |||||
| chr11:43816980
|
ATATATCT others(29): Show |
A | 16 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0051others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+619_501+654del others(36): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | |||||
| chr11:43816996
|
ATCTATAT others(31): Show |
A | 1 | a0001c0001t0001g0028 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.501+607_501+644del others(38): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816996 | |||||
| chr11:43816998
|
C | CTA | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+611_501+612dup others(2): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816998 | |||||
| chr11:43816998
|
CTATATCT others(45): Show |
C | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.501+613_501+664del others(52): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816998 | |||||
| chr11:43817002
|
ATCTATAT others(31): Show |
A | 21 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0034others(18): Show | 21 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.501+613_501+650del others(38): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817002 | |||||
| chr11:43817004
|
CTATATCT others(19): Show |
C | 19 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0266others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.501+617_501+642del others(26): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817004 | |||||
| chr11:43817004
|
CTATATCT others(31): Show |
C | 50 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0033others(47): Show | 50 | HG00408.hp1 HG00423.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.501+619_501+656del others(38): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817004 | |||||
| chr11:43817006
|
ATATCTAT others(15): Show |
A | 1 | a0001c0003t0001g0238 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.501+619_501+640del others(22): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817006 | |||||
| chr11:43817006
|
ATATCTAT others(21): Show |
A | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(33): Show | 36 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.501+619_501+646del others(28): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817006 | |||||
| chr11:43817010
|
CTATATCT others(25): Show |
C | 2 | a0001c0001t0001g0085a0001c0001t0001g0113 | 2 | HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.501+625_501+656del others(32): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817010 | |||||
| chr11:43817018
|
ATATC | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+631_501+634del others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817018 | |||||
| chr11:43817018
|
ATATCTAT others(9): Show |
A | 5 | a0001c0001t0003g0013a0001c0001t0003g0015a0001c0001t0003g0017others(2): Show | 5 | NA18945.hp1 NA18948.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+631_501+646del others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817018 | |||||
| chr11:43817024
|
ATATCTAT others(9): Show |
A | 1 | a0001c0001t0003g0093 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.501+637_501+652del others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817024 | |||||
| chr11:43817028
|
C | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+637C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817028 | ||||||
| chr11:43817030
|
A | C | 1 | a0001c0003t0001g0238 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.501+639A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817030 | ||||||
| chr11:43817034
|
C | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.501+643C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817034 | ||||||
| chr11:43817034
|
CTATATCT others(5): Show |
C | 1 | a0002c0002t0002g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.501+649_501+660del others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817034 | |||||
| chr11:43817036
|
A | C | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(33): Show | 36 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.501+645A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817036 | ||||||
| chr11:43817038
|
A | C | 19 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0266others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.501+647A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817038 | ||||||
| chr11:43817040
|
C | A | 44 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0049others(41): Show | 44 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.501+649C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817040 | ||||||
| chr11:43817053
|
T | G | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.501+662T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817053 | ||||||
| chr11:43817058
|
A | C | 23 | a0002c0002t0002g0024a0002c0002t0002g0108a0002c0002t0002g0115others(20): Show | 23 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.501+667A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817058 | ||||||
| chr11:43817104
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.501+713A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817104 | ||||||
| chr11:43817214
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.501+823G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817214 | ||||||
| chr11:43817474
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.501+1083T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817474 | ||||||
| chr11:43817793
|
C | T | 1 | a0001c0003t0001g0238 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.501+1402C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817793 | ||||||
| chr11:43817881
|
A | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.501+1490A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817881 | ||||||
| chr11:43818214
|
C | T | 13 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.501+1823C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43818214 | ||||||
| chr11:43818385
|
G | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.501+1994G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43818385 | ||||||
| chr11:43819052
|
T | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.501+2661T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43819052 | ||||||
| chr11:43819067
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.501+2676C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43819067 | ||||||
| chr11:43819189
|
T | A | 1 | a0001c0003t0001g0238 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.501+2798T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43819189 | ||||||
| chr11:43819371
|
A | G | 1 | a0001c0001t0003g0013 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.501+2980A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43819371 | ||||||
| chr11:43819996
|
G | T | 1 | a0001c0001t0001g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.501+3605G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43819996 | ||||||
| chr11:43820244
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+3853G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43820244 | ||||||
| chr11:43820441
|
A | G | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.501+4050A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43820441 | ||||||
| chr11:43820499
|
A | T | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+4108A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43820499 | ||||||
| chr11:43820867
|
G | A | 1 | a0002c0002t0002g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.501+4476G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43820867 | ||||||
| chr11:43820952
|
A | T | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+4561A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43820952 | ||||||
| chr11:43820968
|
A | G | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.501+4577A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43820968 | ||||||
| chr11:43821228
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.501+4837A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821228 | ||||||
| chr11:43821501
|
C | T | 13 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.501+5110C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821501 | ||||||
| chr11:43821651
|
T | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.501+5260T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821651 | ||||||
| chr11:43821659
|
A | G | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.501+5268A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821659 | ||||||
| chr11:43821788
|
T | A | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.501+5397T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821788 | ||||||
| chr11:43821899
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.501+5508A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821899 | ||||||
| chr11:43821952
|
T | C | 7 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(4): Show | 7 | HG01109.hp1 HG01496.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.501+5561T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821952 | ||||||
| chr11:43822029
|
C | G | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.501+5638C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43822029 | ||||||
| chr11:43822419
|
G | A | 13 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.501+6028G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43822419 | ||||||
| chr11:43822449
|
A | G | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+6058A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43822449 | ||||||
| chr11:43822630
|
C | G | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.501+6239C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43822630 | ||||||
| chr11:43822650
|
C | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.501+6259C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43822650 | ||||||
| chr11:43822950
|
C | T | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.501+6559C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43822950 | ||||||
| chr11:43823357
|
A | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+6966A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823357 | ||||||
| chr11:43823373
|
C | T | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.501+6982C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823373 | ||||||
| chr11:43823688
|
G | A | 2 | a0001c0001t0003g0012a0001c0001t0003g0018 | 2 | NA19005.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.502-7288G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823688 | ||||||
| chr11:43823733
|
A | T | 1 | a0001c0001t0001g0215 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.502-7243A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823733 | ||||||
| chr11:43823824
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.502-7152C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823824 | ||||||
| chr11:43823869
|
G | A | 1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.502-7107G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823869 | ||||||
| chr11:43823895
|
G | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.502-7081G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823895 | ||||||
| chr11:43824048
|
GA | G | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.502-6927delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824048 | ||||||
| chr11:43824263
|
G | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.502-6713G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824263 | ||||||
| chr11:43824290
|
T | G | 1 | a0001c0003t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.502-6686T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824290 | ||||||
| chr11:43824348
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.502-6628C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824348 | ||||||
| chr11:43824503
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.502-6473G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824503 | ||||||
| chr11:43824567
|
C | G | 1 | a0002c0002t0002g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.502-6409C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824567 | ||||||
| chr11:43824957
|
C | G | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.502-6019C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824957 | ||||||
| chr11:43825008
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.502-5968G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43825008 | ||||||
| chr11:43825130
|
C | CA | 149 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.502-5832dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43825130 | |||||
| chr11:43825147
|
T | C | 18 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.502-5829T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43825147 | ||||||
| chr11:43825155
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-5821A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43825155 | ||||||
| chr11:43825300
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-5676T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43825300 | ||||||
| chr11:43825555
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.502-5421G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43825555 | ||||||
| chr11:43825651
|
C | A | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.502-5325C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43825651 | ||||||
| chr11:43825939
|
AATT | A | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.502-5033_502-5031d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43825939 | |||||
| chr11:43826081
|
C | CT | 25 | a0001c0001t0001g0112a0001c0001t0003g0013a0001c0001t0003g0014others(22): Show | 25 | HG00280.hp1 HG00609.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.502-4876dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43826081 | |||||
| chr11:43826081
|
C | T | 1 | a0002c0002t0002g0149 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.502-4895C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826081 | ||||||
| chr11:43826085
|
T | TC | 160 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.502-4891_502-4890i others(3): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826085 | ||||||
| chr11:43826086
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.502-4890T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826086 | ||||||
| chr11:43826089
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.502-4887T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826089 | ||||||
| chr11:43826090
|
T | C | 93 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(90): Show | 93 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.502-4886T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826090 | ||||||
| chr11:43826109
|
G | T | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.502-4867G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826109 | ||||||
| chr11:43826143
|
C | A | 1 | a0001c0003t0001g0236 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.502-4833C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826143 | ||||||
| chr11:43826163
|
A | T | 1 | a0001c0001t0001g0103 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.502-4813A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826163 | ||||||
| chr11:43826361
|
G | A | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.502-4615G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826361 | ||||||
| chr11:43826655
|
AAT | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.502-4319_502-4318d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43826655 | |||||
| chr11:43826752
|
CTAAGAA | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.502-4222_502-4217d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43826752 | |||||
| chr11:43826788
|
G | A | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.502-4188G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826788 | ||||||
| chr11:43826889
|
G | T | 20 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(17): Show | 20 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.502-4087G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826889 | ||||||
| chr11:43827095
|
C | T | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.502-3881C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827095 | ||||||
| chr11:43827204
|
C | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-3772C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827204 | ||||||
| chr11:43827253
|
G | A | 1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.502-3723G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827253 | ||||||
| chr11:43827326
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.502-3650C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827326 | ||||||
| chr11:43827327
|
T | TA | 4 | a0001c0007t0001g0232a0002c0002t0004g0206a0002c0002t0004g0275others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-3643dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43827327 | |||||
| chr11:43827556
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.502-3420A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827556 | ||||||
| chr11:43827570
|
A | G | 72 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(69): Show | 72 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.502-3406A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827570 | ||||||
| chr11:43827743
|
C | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-3233C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827743 | ||||||
| chr11:43828045
|
T | C | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.502-2931T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828045 | ||||||
| chr11:43828074
|
C | A | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.502-2902C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828074 | ||||||
| chr11:43828141
|
C | CT | 9 | a0001c0001t0001g0008a0001c0001t0001g0053a0001c0001t0001g0092others(6): Show | 9 | HG01258.hp1 HG01261.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.502-2816dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43828141 | |||||
| chr11:43828141
|
CT | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0076a0001c0001t0001g0222others(6): Show | 9 | HG01884.hp1 HG02602.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.502-2816delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43828141 | |||||
| chr11:43828256
|
C | G | 1 | a0001c0003t0001g0228 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.502-2720C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828256 | ||||||
| chr11:43828334
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-2642A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828334 | ||||||
| chr11:43828363
|
C | T | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.502-2613C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828363 | ||||||
| chr11:43828385
|
G | GC | 278 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.502-2589dupC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43828385 | |||||
| chr11:43828437
|
G | A | 2 | a0002c0002t0002g0139a0002c0002t0002g0186 | 2 | HG00639.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.502-2539G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828437 | ||||||
| chr11:43828527
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.502-2449A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828527 | ||||||
| chr11:43828566
|
C | T | 1 | a0002c0002t0002g0256 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.502-2410C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828566 | ||||||
| chr11:43828616
|
CAA | C | 5 | a0002c0002t0002g0171a0002c0002t0002g0172a0002c0002t0002g0176others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.502-2356_502-2355d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43828616 | |||||
| chr11:43828873
|
C | T | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.502-2103C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828873 | ||||||
| chr11:43829089
|
A | G | 1 | a0001c0003t0001g0238 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.502-1887A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829089 | ||||||
| chr11:43829175
|
T | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.502-1801T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829175 | ||||||
| chr11:43829189
|
C | T | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.502-1787C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829189 | ||||||
| chr11:43829736
|
CTCCT | C | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.502-1234_502-1231d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43829736 | |||||
| chr11:43829758
|
G | T | 48 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0044others(45): Show | 48 | HG00408.hp1 HG00423.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.502-1218G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829758 | ||||||
| chr11:43829797
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.502-1179T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829797 | ||||||
| chr11:43829924
|
A | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.502-1052A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829924 | ||||||
| chr11:43829947
|
T | C | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0271 | 3 | HG02451.hp2 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.502-1029T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829947 | ||||||
| chr11:43829948
|
A | G | 2 | a0002c0002t0002g0169a0002c0002t0002g0170 | 2 | NA18962.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.502-1028A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829948 | ||||||
| chr11:43830170
|
T | C | 1 | a0002c0002t0010g0158 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.502-806T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830170 | ||||||
| chr11:43830213
|
T | C | 1 | a0001c0001t0001g0258 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.502-763T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830213 | ||||||
| chr11:43830253
|
G | A | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.502-723G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830253 | ||||||
| chr11:43830462
|
T | G | 1 | a0001c0001t0001g0203 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.502-514T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830462 | ||||||
| chr11:43830533
|
C | T | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.502-443C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830533 | ||||||
| chr11:43830547
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.502-429G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830547 | ||||||
| chr11:43830630
|
A | G | 21 | a0001c0001t0001g0187a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.502-346A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830630 | ||||||
| chr11:43830820
|
G | C | 5 | a0002c0002t0002g0171a0002c0002t0002g0172a0002c0002t0002g0176others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.502-156G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830820 | ||||||
| chr11:43830941
|
T | C | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.502-35T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830941 | ||||||
| chr11:43830955
|
G | A | 1 | a0002c0002t0002g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.502-21G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830955 | ||||||
| chr11:43831080
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.536+70C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43831080 | ||||||
| chr11:43831339
|
T | C | 14 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(11): Show | 14 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.536+329T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43831339 | ||||||
| chr11:43831376
|
A | G | 6 | a0002c0002t0002g0108a0002c0002t0002g0169a0002c0002t0002g0170others(3): Show | 6 | HG00423.hp1 NA18944.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.536+366A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43831376 | ||||||
| chr11:43831511
|
G | A | 1 | a0002c0002t0002g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.536+501G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43831511 | ||||||
| chr11:43831565
|
A | G | 72 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(69): Show | 72 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.536+555A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43831565 | ||||||
| chr11:43831830
|
T | C | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.536+820T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43831830 | ||||||
| chr11:43832359
|
T | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.536+1349T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43832359 | ||||||
| chr11:43832458
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.536+1448C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43832458 | ||||||
| chr11:43832471
|
C | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0114 | 2 | NA19068.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.536+1461C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43832471 | ||||||
| chr11:43832701
|
C | A | 1 | a0001c0003t0001g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.536+1691C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43832701 | ||||||
| chr11:43832799
|
G | T | 9 | a0001c0003t0003g0234a0001c0003t0003g0235a0001c0003t0003g0245others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.536+1789G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43832799 | ||||||
| chr11:43833032
|
C | CA | 35 | a0002c0002t0002g0003a0002c0002t0002g0024a0002c0002t0002g0108others(32): Show | 35 | HG00423.hp1 HG00738.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.536+2044dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 43833032 | |||||
| chr11:43833032
|
CAAAAAA | C | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.536+2039_536+2044d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 43833032 | |||||
| chr11:43833060
|
G | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.536+2050G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833060 | ||||||
| chr11:43833146
|
A | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.536+2136A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833146 | ||||||
| chr11:43833360
|
G | C | 73 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(70): Show | 73 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.536+2350G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833360 | ||||||
| chr11:43833522
|
A | G | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.536+2512A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833522 | ||||||
| chr11:43833739
|
TTTG | T | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.536+2738_536+2740d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 43833739 | |||||
| chr11:43833758
|
C | T | 3 | a0002c0002t0004g0206a0002c0002t0004g0275a0002c0002t0009g0201 | 3 | HG02451.hp1 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.536+2748C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833758 | ||||||
| chr11:43833940
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.536+2930A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833940 | ||||||
| chr11:43833943
|
G | A | 2 | a0002c0002t0002g0171a0002c0002t0002g0172 | 2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.536+2933G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833943 | ||||||
| chr11:43834243
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.536+3233C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43834243 | ||||||
| chr11:43834368
|
AT | A | 153 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.536+3371delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 43834368 | |||||
| chr11:43834574
|
A | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.536+3564A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43834574 | ||||||
| chr11:43834748
|
A | G | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0203others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.537-3569A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43834748 | ||||||
| chr11:43834771
|
T | G | 95 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(92): Show | 95 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.537-3546T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43834771 | ||||||
| chr11:43834805
|
G | T | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.537-3512G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43834805 | ||||||
| chr11:43834885
|
GT | G | 12 | a0002c0002t0002g0003a0002c0002t0002g0138a0002c0002t0002g0142others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.537-3426delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 43834885 | |||||
| chr11:43835613
|
T | A | 14 | a0001c0003t0003g0234a0001c0003t0003g0235a0001c0003t0003g0245others(11): Show | 14 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.537-2704T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43835613 | ||||||
| chr11:43835656
|
G | C | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.537-2661G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43835656 | ||||||
| chr11:43835868
|
A | G | 163 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.537-2449A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43835868 | ||||||
| chr11:43835908
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.537-2409A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43835908 | ||||||
| chr11:43836357
|
G | T | 1 | a0002c0002t0002g0169 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.537-1960G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43836357 | ||||||
| chr11:43836378
|
G | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.537-1939G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43836378 | ||||||
| chr11:43836725
|
A | G | 1 | a0002c0002t0002g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.537-1592A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43836725 | ||||||
| chr11:43836748
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0052 | 3 | HG02135.hp2 NA19070.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.537-1569T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43836748 | ||||||
| chr11:43836818
|
A | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.537-1499A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43836818 | ||||||
| chr11:43837001
|
T | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.537-1316T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43837001 | ||||||
| chr11:43837004
|
G | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.537-1313G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43837004 | ||||||
| chr11:43837132
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.537-1185A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43837132 | ||||||
| chr11:43837513
|
C | T | 20 | a0001c0001t0001g0187a0001c0001t0001g0209a0001c0001t0001g0210others(17): Show | 20 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.537-804C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43837513 | ||||||
| chr11:43837937
|
G | C | 1 | a0001c0003t0001g0236 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.537-380G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43837937 | ||||||
| chr11:43837969
|
G | C | 2 | a0002c0002t0002g0178a0002c0002t0002g0263 | 2 | HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.537-348G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43837969 | ||||||
| chr11:43838066
|
A | T | 1 | a0001c0003t0003g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.537-251A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43838066 | ||||||
| chr11:43838120
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.537-197A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43838120 | ||||||
| chr11:43838467
|
G | A | 4 | a0002c0002t0002g0116a0002c0002t0002g0117a0002c0002t0002g0118others(1): Show | 4 | HG00408.hp2 HG02135.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+69G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43838467 | ||||||
| chr11:43838650
|
T | TC | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.618+258dupC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 43838650 | |||||
| chr11:43838750
|
G | A | 77 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(74): Show | 77 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.618+352G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43838750 | ||||||
| chr11:43838840
|
G | T | 1 | a0002c0002t0002g0141 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.618+442G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43838840 | ||||||
| chr11:43839017
|
G | A | 4 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0018others(1): Show | 4 | NA18612.hp2 NA18747.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+619G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839017 | ||||||
| chr11:43839042
|
G | A | 1 | a0002c0002t0004g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.618+644G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839042 | ||||||
| chr11:43839093
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.618+695A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839093 | ||||||
| chr11:43839382
|
A | C | 18 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.619-617A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839382 | ||||||
| chr11:43839547
|
C | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.619-452C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839547 | ||||||
| chr11:43839703
|
T | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.619-296T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839703 | ||||||
| chr11:43839745
|
G | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0114 | 2 | NA19068.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.619-254G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839745 | ||||||
| chr11:43839901
|
G | A | 1 | a0002c0002t0002g0185 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.619-98G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839901 | ||||||
| chr11:43840198
|
G | A | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.684+134G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840198 | ||||||
| chr11:43840387
|
T | C | 1 | a0002c0002t0002g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.684+323T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840387 | ||||||
| chr11:43840503
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.684+439A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840503 | ||||||
| chr11:43840570
|
C | CACTAGTT others(3): Show |
19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+506_684+507ins others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840570 | ||||||
| chr11:43840572
|
A | T | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+508A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840572 | ||||||
| chr11:43840582
|
A | G | 73 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(70): Show | 73 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.684+518A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840582 | ||||||
| chr11:43840775
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.684+711T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840775 | ||||||
| chr11:43840827
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.684+763A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840827 | ||||||
| chr11:43840958
|
T | C | 3 | a0002c0002t0002g0131a0002c0002t0002g0136a0002c0002t0002g0137 | 3 | NA18943.hp2 NA18952.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.684+894T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840958 | ||||||
| chr11:43841326
|
G | T | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+1262G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43841326 | ||||||
| chr11:43841480
|
G | A | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.684+1416G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43841480 | ||||||
| chr11:43841607
|
T | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0094 | 2 | NA18949.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.684+1543T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43841607 | ||||||
| chr11:43841780
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0083 | 2 | HG01123.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.684+1716C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43841780 | ||||||
| chr11:43841793
|
T | C | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+1729T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43841793 | ||||||
| chr11:43841947
|
C | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0078 | 2 | NA18941.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.684+1883C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43841947 | ||||||
| chr11:43842156
|
G | A | 1 | a0001c0001t0003g0019 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.684+2092G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842156 | ||||||
| chr11:43842305
|
G | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0052 | 3 | HG02135.hp2 NA19070.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.684+2241G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842305 | ||||||
| chr11:43842313
|
A | C | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+2249A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842313 | ||||||
| chr11:43842326
|
G | A | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+2262G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842326 | ||||||
| chr11:43842352
|
G | A | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+2288G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842352 | ||||||
| chr11:43842352
|
G | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00738.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.684+2288G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842352 | ||||||
| chr11:43842383
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0051 | 2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.684+2319C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842383 | ||||||
| chr11:43842540
|
C | T | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0126 | 3 | HG01884.hp2 HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.684+2476C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842540 | ||||||
| chr11:43842728
|
T | C | 205 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.684+2664T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842728 | ||||||
| chr11:43842894
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.684+2830G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842894 | ||||||
| chr11:43843391
|
C | A | 8 | a0002c0002t0002g0128a0002c0002t0002g0140a0002c0002t0002g0147others(5): Show | 8 | HG00140.hp2 HG01070.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.684+3327C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43843391 | ||||||
| chr11:43843597
|
GC | G | 6 | a0002c0002t0002g0003a0002c0002t0002g0145a0002c0002t0002g0153others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.684+3536delC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43843597 | |||||
| chr11:43843865
|
C | A | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+3801C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43843865 | ||||||
| chr11:43843910
|
G | A | 1 | a0002c0002t0002g0127 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.684+3846G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43843910 | ||||||
| chr11:43843947
|
T | C | 5 | a0002c0002t0002g0171a0002c0002t0002g0172a0002c0002t0002g0176others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+3883T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43843947 | ||||||
| chr11:43843951
|
A | G | 73 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(70): Show | 73 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.684+3887A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43843951 | ||||||
| chr11:43844164
|
C | T | 1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.684+4100C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43844164 | ||||||
| chr11:43844169
|
G | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.684+4105G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43844169 | ||||||
| chr11:43844338
|
C | A | 1 | a0001c0001t0001g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.684+4274C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43844338 | ||||||
| chr11:43844687
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.684+4623G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43844687 | ||||||
| chr11:43844744
|
T | A | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.684+4680T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43844744 | ||||||
| chr11:43844981
|
G | GTTGT | 78 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(75): Show | 78 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.684+4939_684+4942d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43844981 | |||||
| chr11:43844981
|
GTTGT | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.684+4939_684+4942d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43844981 | |||||
| chr11:43845352
|
T | C | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.684+5288T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43845352 | ||||||
| chr11:43845362
|
T | C | 1 | a0001c0003t0001g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.684+5298T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43845362 | ||||||
| chr11:43845392
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.684+5328C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43845392 | ||||||
| chr11:43845470
|
CTT | C | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.684+5409_684+5410d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43845470 | |||||
| chr11:43845725
|
C | T | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.684+5661C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43845725 | ||||||
| chr11:43845726
|
G | A | 1 | a0001c0003t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.684+5662G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43845726 | ||||||
| chr11:43846048
|
G | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+5984G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846048 | ||||||
| chr11:43846098
|
G | T | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.684+6034G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846098 | ||||||
| chr11:43846102
|
G | A | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.684+6038G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846102 | ||||||
| chr11:43846373
|
G | A | 2 | a0002c0002t0002g0191a0002c0002t0002g0192 | 2 | NA18982.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.684+6309G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846373 | ||||||
| chr11:43846392
|
G | A | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+6328G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846392 | ||||||
| chr11:43846493
|
G | A | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.684+6429G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846493 | ||||||
| chr11:43846818
|
C | G | 222 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.684+6754C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846818 | ||||||
| chr11:43846839
|
C | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0052 | 3 | HG02135.hp2 NA19070.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.684+6775C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846839 | ||||||
| chr11:43847031
|
T | C | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.684+6967T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847031 | ||||||
| chr11:43847087
|
TAG | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.684+7029_684+7030d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847087 | |||||
| chr11:43847101
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.684+7037T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847101 | ||||||
| chr11:43847170
|
G | A | 1 | a0002c0002t0002g0143 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.684+7106G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847170 | ||||||
| chr11:43847632
|
A | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.685-7083A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847632 | ||||||
| chr11:43847659
|
A | G | 1 | a0002c0002t0009g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.685-7056A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847659 | ||||||
| chr11:43847664
|
GTCACTGC others(2): Show |
G | 9 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 9 | HG01261.hp2 HG01884.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-7048_685-7040d others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847664 | |||||
| chr11:43847715
|
C | CAAA | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(13): Show | 16 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.685-6984_685-6982d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | |||||
| chr11:43847715
|
C | CAAAA | 74 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(71): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.685-6985_685-6982d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | |||||
| chr11:43847715
|
C | CAAAAA | 22 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0058others(19): Show | 22 | HG01123.hp1 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.685-6986_685-6982d others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | |||||
| chr11:43847715
|
C | CAAAAAAA others(2): Show |
37 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.685-6990_685-6982d others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | |||||
| chr11:43847715
|
C | CAAAAAAA others(3): Show |
18 | a0001c0001t0001g0130a0001c0001t0001g0187a0001c0001t0001g0209others(15): Show | 18 | HG01069.hp1 HG01106.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.685-6991_685-6982d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | |||||
| chr11:43847715
|
C | CAAAAAAA others(4): Show |
9 | a0001c0001t0003g0279a0001c0003t0001g0274a0001c0003t0003g0245others(6): Show | 9 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-6992_685-6982d others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | |||||
| chr11:43847715
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0011g0270 | 3 | HG02572.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.685-6993_685-6982d others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | |||||
| chr11:43847715
|
C | CAAAAAAA others(10): Show |
2 | a0001c0003t0001g0233a0002c0002t0008g0002 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.685-6998_685-6982d others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | |||||
| chr11:43847811
|
T | C | 1 | a0002c0002t0002g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.685-6904T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847811 | ||||||
| chr11:43847931
|
A | G | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.685-6784A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847931 | ||||||
| chr11:43848120
|
G | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.685-6595G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848120 | ||||||
| chr11:43848273
|
C | T | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.685-6442C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848273 | ||||||
| chr11:43848295
|
G | A | 1 | a0001c0003t0001g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.685-6420G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848295 | ||||||
| chr11:43848310
|
C | G | 222 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.685-6405C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848310 | ||||||
| chr11:43848354
|
C | T | 7 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.685-6361C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848354 | ||||||
| chr11:43848389
|
G | A | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.685-6326G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848389 | ||||||
| chr11:43848430
|
C | T | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.685-6285C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848430 | ||||||
| chr11:43848673
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0069 | 2 | NA18945.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.685-6042G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848673 | ||||||
| chr11:43849321
|
C | CA | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.685-5387dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43849321 | |||||
| chr11:43849325
|
A | AC | 3 | a0003c0004t0001g0231a0003c0004t0001g0244a0003c0004t0001g0252 | 3 | HG02647.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.685-5390_685-5389i others(3): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43849325 | ||||||
| chr11:43849629
|
C | A | 1 | a0001c0001t0001g0043 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.685-5086C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43849629 | ||||||
| chr11:43849662
|
C | G | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.685-5053C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43849662 | ||||||
| chr11:43849805
|
T | C | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.685-4910T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43849805 | ||||||
| chr11:43849975
|
G | A | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.685-4740G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43849975 | ||||||
| chr11:43850032
|
C | A | 1 | a0002c0002t0002g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.685-4683C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850032 | ||||||
| chr11:43850128
|
C | T | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.685-4587C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850128 | ||||||
| chr11:43850247
|
G | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.685-4468G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850247 | ||||||
| chr11:43850446
|
A | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.685-4269A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850446 | ||||||
| chr11:43850905
|
T | C | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.685-3810T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850905 | ||||||
| chr11:43850934
|
G | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0204others(1): Show | 4 | HG02055.hp1 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-3781G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850934 | ||||||
| chr11:43850967
|
A | C | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.685-3748A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850967 | ||||||
| chr11:43851356
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.685-3359T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43851356 | ||||||
| chr11:43851394
|
C | A | 94 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.685-3321C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43851394 | ||||||
| chr11:43851456
|
T | C | 2 | a0002c0002t0002g0150a0002c0002t0002g0160 | 2 | HG00609.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.685-3259T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43851456 | ||||||
| chr11:43851798
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.685-2917G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43851798 | ||||||
| chr11:43851828
|
T | C | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.685-2887T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43851828 | ||||||
| chr11:43851989
|
C | A | 39 | a0002c0002t0002g0003a0002c0002t0002g0024a0002c0002t0002g0108others(36): Show | 39 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.685-2726C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43851989 | ||||||
| chr11:43852064
|
C | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0052 | 3 | HG02135.hp2 NA19070.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.685-2651C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852064 | ||||||
| chr11:43852085
|
T | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.685-2630T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852085 | ||||||
| chr11:43852184
|
C | T | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.685-2531C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852184 | ||||||
| chr11:43852189
|
G | A | 1 | a0002c0002t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.685-2526G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852189 | ||||||
| chr11:43852274
|
A | G | 3 | a0003c0004t0001g0231a0003c0004t0001g0244a0003c0004t0001g0252 | 3 | HG02647.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.685-2441A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852274 | ||||||
| chr11:43852353
|
A | G | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.685-2362A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852353 | ||||||
| chr11:43852369
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.685-2346G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852369 | ||||||
| chr11:43852459
|
G | GT | 38 | a0001c0001t0001g0037a0001c0001t0001g0110a0001c0001t0001g0111others(35): Show | 38 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.685-2245dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43852459 | |||||
| chr11:43852459
|
G | GTT | 71 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(68): Show | 71 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.685-2246_685-2245d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43852459 | |||||
| chr11:43852500
|
T | C | 4 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0279others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-2215T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852500 | ||||||
| chr11:43852516
|
G | T | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.685-2199G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852516 | ||||||
| chr11:43852674
|
C | T | 4 | a0002c0002t0002g0163a0002c0002t0002g0181a0004c0005t0002g0010others(1): Show | 4 | HG00323.hp1 HG01099.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-2041C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852674 | ||||||
| chr11:43852731
|
C | A | 7 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(4): Show | 7 | HG01928.hp2 HG02523.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-1984C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852731 | ||||||
| chr11:43852751
|
A | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0052 | 3 | HG02135.hp2 NA19070.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.685-1964A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852751 | ||||||
| chr11:43853123
|
G | C | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.685-1592G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853123 | ||||||
| chr11:43853178
|
A | T | 1 | a0002c0002t0002g0254 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.685-1537A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853178 | ||||||
| chr11:43853329
|
C | T | 28 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 28 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.685-1386C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853329 | ||||||
| chr11:43853337
|
C | CA | 62 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0029others(59): Show | 62 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.685-1351dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853337 | |||||
| chr11:43853337
|
C | CAA | 25 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0040others(22): Show | 25 | HG00738.hp2 HG01175.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.685-1352_685-1351d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853337 | |||||
| chr11:43853337
|
CA | C | 16 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0264others(13): Show | 16 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.685-1351delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853337 | |||||
| chr11:43853337
|
CAAAAAAA others(2): Show |
C | 93 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0024others(90): Show | 94 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.685-1359_685-1351d others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853337 | |||||
| chr11:43853337
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0007t0001g0232a0002c0002t0009g0201 | 2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.685-1360_685-1351d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853337 | |||||
| chr11:43853337
|
CAAAAAAA others(6): Show |
C | 28 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 28 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.685-1363_685-1351d others(15): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853337 | |||||
| chr11:43853404
|
C | T | 1 | a0001c0001t0003g0018 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.685-1311C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853404 | ||||||
| chr11:43853633
|
T | A | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.685-1082T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853633 | ||||||
| chr11:43853762
|
C | G | 14 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.685-953C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853762 | ||||||
| chr11:43853766
|
G | A | 99 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0024others(96): Show | 100 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.685-949G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853766 | ||||||
| chr11:43853819
|
TATC | T | 99 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0024others(96): Show | 100 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.685-893_685-891del others(3): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853819 | |||||
| chr11:43854024
|
G | C | 2 | a0002c0002t0004g0206a0002c0002t0004g0275 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.685-691G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854024 | ||||||
| chr11:43854145
|
G | A | 4 | a0002c0002t0002g0116a0002c0002t0002g0117a0002c0002t0002g0118others(1): Show | 4 | HG00408.hp2 HG02135.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-570G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854145 | ||||||
| chr11:43854164
|
T | C | 99 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0024others(96): Show | 100 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.685-551T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854164 | ||||||
| chr11:43854224
|
C | T | 2 | a0002c0002t0002g0191a0002c0002t0002g0192 | 2 | NA18982.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.685-491C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854224 | ||||||
| chr11:43854464
|
A | G | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.685-251A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854464 | ||||||
| chr11:43854532
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.685-183A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854532 | ||||||
| chr11:43854586
|
C | G | 1 | a0001c0007t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.685-129C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854586 | ||||||
| chr11:43854885
|
A | G | 100 | a0001c0007t0001g0232a0002c0002t0002g0001a0002c0002t0002g0003others(97): Show | 101 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.834+21A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 10/10 | chr11 | 43854885 | ||||||
| chr11:43854990
|
A | G | 28 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 28 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.834+126A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 10/10 | chr11 | 43854990 | ||||||
| chr11:43855059
|
C | T | 1 | a0001c0001t0003g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.835-85C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 10/10 | chr11 | 43855059 |