| geneid | 23253 |
|---|---|
| ensemblid | ENSG00000101745.17 |
| hgncid | 29135 |
| symbol | ANKRD12 |
| name | ankyrin repeat domain 12 |
| refseq_nuc | NM_015208.5 |
| refseq_prot | NP_056023.3 |
| ensembl_nuc | ENST00000262126.9 |
| ensembl_prot | ENSP00000262126.3 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 9136781 |
| end | 9285985 |
| strand | + |
| ver | v1.2 |
| region | chr18:9136781-9285985 |
| region5000 | chr18:9131781-9290985 |
| regionname0 | ANKRD12_chr18_9136781_9285985 |
| regionname5000 | ANKRD12_chr18_9131781_9290985 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 2062 | 139 | 32 | 24 | 57 | 8 | 17 | 44 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002 | 1/0 | 2062 | 81 | 37 | 17 | 16 | 3 | 7 | 13 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0003 | 0/0 | 2062 | 44 | 1 | 3 | 36 | 1 | 3 | 33 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0004 | 0/0 | 2062 | 34 | 7 | 2 | 23 | 1 | 1 | 20 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0005 | 0/0 | 2062 | 5 | 0 | 4 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0006 | 0/0 | 2062 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0007 | 0/0 | 2062 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0008 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0009 | 0/0 | 2062 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0010 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0011 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0012 | 0/0 | 2062 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0013 | 0/0 | 2062 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0014 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0015 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0016 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 6189 | 129 | 25 | 24 | 57 | 8 | 14 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0002 | 1/0 | 6189 | 74 | 34 | 13 | 16 | 3 | 7 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0003 | 0/0 | 6189 | 44 | 1 | 3 | 36 | 1 | 3 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0004 | 0/0 | 6189 | 33 | 7 | 2 | 22 | 1 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0005 | 0/0 | 6189 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0006 | 0/0 | 6189 | 5 | 0 | 4 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0007 | 0/0 | 6189 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0008 | 0/0 | 6189 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0009 | 0/0 | 6189 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0010 | 0/0 | 6189 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0011 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0012 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0013 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0014 | 0/0 | 6189 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0015 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0016 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0017 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0018 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0019 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0020 | 0/0 | 6189 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0021 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0022 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0023 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0024 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0025 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0026 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0027 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0028 | 0/0 | 6189 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| c0029 | 0/0 | 6189 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| 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 | 5096 | 67 | 8 | 11 | 37 | 3 | 7 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0002 | 0/0 | 5097 | 24 | 0 | 3 | 14 | 0 | 7 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0003 | 0/0 | 5096 | 24 | 6 | 5 | 8 | 1 | 4 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0004 | 0/0 | 5093 | 23 | 1 | 2 | 20 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0005 | 0/0 | 5098 | 19 | 3 | 1 | 13 | 0 | 2 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0006 | 0/0 | 5096 | 16 | 8 | 5 | 0 | 1 | 2 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0007 | 0/0 | 5096 | 9 | 0 | 7 | 0 | 1 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0008 | 0/0 | 5097 | 9 | 1 | 1 | 6 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0009 | 0/0 | 5096 | 8 | 8 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0010 | 0/0 | 5099 | 6 | 0 | 0 | 6 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0011 | 0/0 | 5092 | 6 | 0 | 1 | 5 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0012 | 0/0 | 5093 | 5 | 0 | 2 | 0 | 3 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0013 | 0/0 | 5096 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0014 | 0/0 | 5094 | 4 | 3 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0015 | 0/0 | 5096 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0016 | 0/1 | 5097 | 4 | 1 | 1 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0017 | 0/0 | 5096 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0018 | 0/0 | 5094 | 3 | 1 | 0 | 2 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0019 | 0/0 | 5096 | 3 | 2 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0020 | 0/0 | 5096 | 3 | 0 | 2 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0021 | 0/0 | 5096 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0022 | 0/0 | 5097 | 3 | 2 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0023 | 0/0 | 5096 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0024 | 0/0 | 5095 | 2 | 0 | 0 | 0 | 1 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0025 | 0/0 | 5097 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0026 | 0/0 | 5096 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0027 | 0/0 | 5097 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0028 | 0/0 | 5096 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0029 | 0/0 | 5096 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0030 | 0/0 | 5096 | 2 | 0 | 1 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0031 | 0/0 | 5096 | 2 | 0 | 0 | 0 | 2 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0032 | 0/0 | 5097 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0033 | 0/0 | 5096 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0034 | 0/0 | 5096 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0035 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0036 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0037 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0038 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0039 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0040 | 0/0 | 5097 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0041 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0042 | 0/0 | 5096 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0043 | 0/0 | 5097 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0044 | 0/0 | 5097 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0045 | 0/0 | 5098 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0046 | 0/0 | 5099 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0047 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0048 | 0/0 | 5098 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0049 | 0/0 | 5096 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0050 | 0/0 | 5098 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0051 | 0/0 | 5097 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0052 | 0/0 | 5096 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0053 | 0/0 | 5097 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0054 | 0/0 | 5098 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0055 | 0/0 | 5098 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0056 | 0/0 | 5097 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0057 | 0/0 | 5095 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0058 | 0/0 | 5097 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0059 | 0/0 | 5096 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0060 | 0/0 | 5096 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0061 | 0/0 | 5096 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0062 | 0/0 | 5097 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0063 | 0/0 | 5096 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0064 | 0/0 | 5092 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0065 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0066 | 0/0 | 5098 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0067 | 0/0 | 5097 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0068 | 0/0 | 5096 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0069 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0070 | 0/0 | 5095 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0071 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0072 | 0/0 | 5096 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0073 | 0/0 | 5097 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0074 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| t0075 | 0/0 | 5098 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| 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 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| 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 | 0/1 | 6189 | 129 | 25 | 24 | 57 | 8 | 14 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0007 | 0/0 | 6189 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0009 | 0/0 | 6189 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0010 | 0/0 | 6189 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0012 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0024 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0029 | 0/0 | 6189 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002 | 1/0 | 6189 | 74 | 34 | 13 | 16 | 3 | 7 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0008 | 0/0 | 6189 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0013 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0015 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0018 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0022 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0025 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0003c0003 | 0/0 | 6189 | 44 | 1 | 3 | 36 | 1 | 3 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0004c0004 | 0/0 | 6189 | 33 | 7 | 2 | 22 | 1 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0004c0028 | 0/0 | 6189 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0005c0006 | 0/0 | 6189 | 5 | 0 | 4 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0006c0005 | 0/0 | 6189 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0007c0027 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0008c0026 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0009c0014 | 0/0 | 6189 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0010c0023 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0011c0017 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0012c0016 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0013c0020 | 0/0 | 6189 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0014c0021 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0015c0019 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0016c0011 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 11285 | 21 | 0 | 3 | 14 | 0 | 4 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0003 | 0/0 | 11284 | 21 | 4 | 5 | 8 | 1 | 3 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0005 | 0/0 | 11286 | 19 | 3 | 1 | 13 | 0 | 2 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0007 | 0/0 | 11284 | 4 | 0 | 3 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0009 | 0/0 | 11284 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0010 | 0/0 | 11287 | 6 | 0 | 0 | 6 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0011 | 0/0 | 11280 | 6 | 0 | 1 | 5 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0012 | 0/0 | 11281 | 5 | 0 | 2 | 0 | 3 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0016 | 0/1 | 11285 | 4 | 1 | 1 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0017 | 0/0 | 11284 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0020 | 0/0 | 11284 | 3 | 0 | 2 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0021 | 0/0 | 11284 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0022 | 0/0 | 11285 | 3 | 2 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0027 | 0/0 | 11285 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0029 | 0/0 | 11284 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0030 | 0/0 | 11284 | 2 | 0 | 1 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0031 | 0/0 | 11284 | 2 | 0 | 0 | 0 | 2 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0034 | 0/0 | 11284 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0041 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0044 | 0/0 | 11285 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0045 | 0/0 | 11286 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0046 | 0/0 | 11287 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0047 | 0/0 | 11282 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0048 | 0/0 | 11286 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0049 | 0/0 | 11284 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0050 | 0/0 | 11286 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0051 | 0/0 | 11285 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0052 | 0/0 | 11284 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0054 | 0/0 | 11286 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0055 | 0/0 | 11286 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0056 | 0/0 | 11285 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0057 | 0/0 | 11283 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0058 | 0/0 | 11285 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0066 | 0/0 | 11286 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0001t0075 | 0/0 | 11286 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0007t0028 | 0/0 | 11284 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0007t0053 | 0/0 | 11285 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0009t0033 | 0/0 | 11284 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0010t0002 | 0/0 | 11285 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0012t0003 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0024t0074 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0001c0029t0002 | 0/0 | 11285 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0001 | 1/0 | 11284 | 32 | 8 | 6 | 12 | 2 | 3 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0006 | 0/0 | 11284 | 13 | 6 | 4 | 0 | 1 | 2 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0008 | 0/0 | 11285 | 5 | 1 | 1 | 2 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0009 | 0/0 | 11284 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0013 | 0/0 | 11284 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0019 | 0/0 | 11284 | 3 | 2 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0025 | 0/0 | 11285 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0026 | 0/0 | 11284 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0032 | 0/0 | 11285 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0043 | 0/0 | 11285 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0059 | 0/0 | 11284 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0061 | 0/0 | 11284 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0067 | 0/0 | 11285 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0068 | 0/0 | 11284 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0069 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0002t0072 | 0/0 | 11284 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0008t0006 | 0/0 | 11284 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0013t0071 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0015t0006 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0018t0042 | 0/0 | 11284 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0022t0064 | 0/0 | 11280 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0002c0025t0001 | 0/0 | 11284 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0003c0003t0001 | 0/0 | 11284 | 32 | 0 | 3 | 25 | 1 | 3 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0003c0003t0008 | 0/0 | 11285 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0003c0003t0023 | 0/0 | 11284 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0003c0003t0060 | 0/0 | 11284 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0003c0003t0062 | 0/0 | 11285 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0003c0003t0063 | 0/0 | 11284 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0003c0003t0065 | 0/0 | 11280 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0003c0003t0073 | 0/0 | 11285 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0004c0004t0004 | 0/0 | 11281 | 21 | 1 | 1 | 19 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0004c0004t0014 | 0/0 | 11282 | 4 | 3 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0004c0004t0018 | 0/0 | 11282 | 3 | 1 | 0 | 2 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0004c0004t0024 | 0/0 | 11283 | 2 | 0 | 0 | 0 | 1 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0004c0004t0036 | 0/0 | 11277 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0004c0004t0037 | 0/0 | 11282 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0004c0004t0038 | 0/0 | 11282 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0004c0028t0004 | 0/0 | 11281 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0005c0006t0007 | 0/0 | 11284 | 5 | 0 | 4 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0006c0005t0015 | 0/0 | 11284 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0006c0005t0040 | 0/0 | 11285 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0007c0027t0004 | 0/0 | 11281 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0008c0026t0039 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0009c0014t0001 | 0/0 | 11284 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0010c0023t0035 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0011c0017t0013 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0012c0016t0001 | 0/0 | 11284 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0013c0020t0003 | 0/0 | 11284 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0014c0021t0003 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0015c0019t0070 | 0/0 | 11283 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| a0016c0011t0013 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | copy fasta | chr18 | 9131781 | 9290985 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0007g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0007g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0010g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0010g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0010g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0010g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0010g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0011g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0011g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0011g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0011g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0011g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0011g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0012g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0012g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0012g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0012g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0012g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0016g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0016g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0016g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0016g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0017g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0017g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0017g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0017g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0020g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0020g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0020g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0021g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0021g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0021g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0022g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0022g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0022g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0027g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0027g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0029g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0029g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0030g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0030g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0031g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0031g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0034g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0034g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0041g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0044g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0045g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0046g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0047g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0048g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0049g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0050g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0051g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0052g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0054g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0055g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0056g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0057g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0058g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0066g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0001t0075g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0007t0028g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0007t0028g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0007t0053g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0009t0033g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0009t0033g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0010t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0010t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0012t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0024t0074g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0001c0029t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0006g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0006g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0006g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0006g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0008g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0008g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0008g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0008g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0013g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0013g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0013g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0019g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0019g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0019g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0025g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0025g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0026g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0026g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0032g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0032g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0043g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0059g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0061g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0067g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0068g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0069g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0002t0072g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0008t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0008t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0013t0071g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0015t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0018t0042g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0022t0064g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0002c0025t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0008g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0008g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0023g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0023g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0023g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0060g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0062g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0063g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0065g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0003c0003t0073g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0014g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0014g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0014g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0014g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0018g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0018g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0018g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0024g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0024g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0036g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0037g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0004t0038g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0004c0028t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0005c0006t0007g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0005c0006t0007g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0005c0006t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0005c0006t0007g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0005c0006t0007g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0006c0005t0015g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0006c0005t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0006c0005t0015g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0006c0005t0015g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0006c0005t0040g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0007c0027t0004g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0008c0026t0039g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0009c0014t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0010c0023t0035g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0011c0017t0013g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0012c0016t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0013c0020t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0014c0021t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0015c0019t0070g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| a0016c0011t0013g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0005 | c0006 | t0007 | g0179 | EUR | GBR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00099 | hp2 | a0001 | c0001 | t0045 | g0208 | EUR | GBR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00140 | hp1 | a0004 | c0004 | t0024 | g0307 | EUR | GBR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00140 | hp2 | a0002 | c0002 | t0006 | g0053 | EUR | GBR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0101 | EUR | FIN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00280 | hp2 | a0001 | c0001 | t0016 | g0184 | EUR | FIN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00323 | hp1 | a0003 | c0003 | t0001 | g0083 | EUR | FIN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00323 | hp2 | a0001 | c0001 | t0012 | g0210 | EUR | FIN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | CHS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00423 | hp2 | a0001 | c0001 | t0011 | g0247 | EAS | CHS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0138 | EAS | CHS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | CHS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00621 | hp1 | a0003 | c0003 | t0001 | g0108 | EAS | CHS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00621 | hp2 | a0001 | c0001 | t0011 | g0241 | EAS | CHS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00639 | hp1 | a0007 | c0027 | t0004 | g0309 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00639 | hp2 | a0001 | c0001 | t0054 | g0003 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0240 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00733 | hp2 | a0002 | c0002 | t0006 | g0051 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0259 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG00735 | hp2 | a0002 | c0002 | t0068 | g0143 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01069 | hp1 | a0001 | c0001 | t0012 | g0212 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01069 | hp2 | a0002 | c0002 | t0008 | g0155 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01070 | hp2 | a0002 | c0002 | t0019 | g0057 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01071 | hp2 | a0001 | c0001 | t0012 | g0213 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0275 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01081 | hp2 | a0002 | c0008 | t0006 | g0049 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01106 | hp1 | a0001 | c0001 | t0020 | g0182 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01106 | hp2 | a0002 | c0018 | t0042 | g0315 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01109 | hp1 | a0012 | c0016 | t0001 | g0079 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0187 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01167 | hp1 | a0002 | c0022 | t0064 | g0316 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01167 | hp2 | a0002 | c0025 | t0001 | g0120 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01168 | hp2 | a0001 | c0001 | t0057 | g0244 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01243 | hp1 | a0002 | c0002 | t0006 | g0038 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0035 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01255 | hp1 | a0005 | c0006 | t0007 | g0178 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01255 | hp2 | a0002 | c0002 | t0006 | g0039 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01256 | hp1 | a0005 | c0006 | t0007 | g0204 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01256 | hp2 | a0001 | c0001 | t0016 | g0177 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0066 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01433 | hp1 | a0001 | c0001 | t0020 | g0183 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0074 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01515 | hp1 | a0001 | c0001 | t0031 | g0317 | EUR | IBS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01515 | hp2 | a0001 | c0001 | t0031 | g0248 | EUR | IBS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01516 | hp1 | a0001 | c0001 | t0012 | g0192 | EUR | IBS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0198 | EUR | IBS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01884 | hp1 | a0006 | c0005 | t0015 | g0008 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01884 | hp2 | a0014 | c0021 | t0003 | g0168 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01891 | hp2 | a0002 | c0002 | t0032 | g0160 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01928 | hp2 | a0005 | c0006 | t0007 | g0270 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01934 | hp1 | a0001 | c0001 | t0027 | g0065 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01934 | hp2 | a0004 | c0004 | t0004 | g0286 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0189 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0076 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01952 | hp1 | a0001 | c0001 | t0011 | g0171 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01952 | hp2 | a0004 | c0004 | t0014 | g0312 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02004 | hp1 | a0005 | c0006 | t0007 | g0176 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02004 | hp2 | a0002 | c0002 | t0006 | g0050 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02015 | hp1 | a0004 | c0004 | t0004 | g0283 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02055 | hp1 | a0001 | c0001 | t0017 | g0029 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02055 | hp2 | a0001 | c0001 | t0022 | g0002 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02071 | hp1 | a0002 | c0002 | t0008 | g0134 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02071 | hp2 | a0001 | c0001 | t0011 | g0250 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0206 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02129 | hp1 | a0001 | c0001 | t0049 | g0180 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02132 | hp1 | a0001 | c0001 | t0021 | g0191 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02132 | hp2 | a0004 | c0004 | t0004 | g0288 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0220 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02135 | hp2 | a0004 | c0004 | t0004 | g0284 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0100 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02148 | hp2 | a0001 | c0001 | t0030 | g0276 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02258 | hp1 | a0001 | c0001 | t0047 | g0214 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0150 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02300 | hp2 | a0001 | c0001 | t0022 | g0170 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02451 | hp1 | a0002 | c0002 | t0006 | g0042 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0116 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0111 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0209 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02572 | hp1 | a0002 | c0002 | t0019 | g0056 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02572 | hp2 | a0001 | c0007 | t0053 | g0027 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0148 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02615 | hp2 | a0004 | c0004 | t0038 | g0310 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02622 | hp1 | a0004 | c0004 | t0014 | g0313 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02622 | hp2 | a0002 | c0002 | t0025 | g0060 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02630 | hp2 | a0006 | c0005 | t0040 | g0166 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02647 | hp1 | a0006 | c0005 | t0015 | g0007 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0024 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0099 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02683 | hp2 | a0001 | c0010 | t0002 | g0175 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02717 | hp1 | a0002 | c0002 | t0009 | g0147 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02717 | hp2 | a0002 | c0002 | t0006 | g0041 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02723 | hp1 | a0004 | c0004 | t0014 | g0311 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02723 | hp2 | a0002 | c0002 | t0006 | g0052 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0271 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02809 | hp1 | a0006 | c0005 | t0015 | g0009 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02809 | hp2 | a0004 | c0004 | t0004 | g0308 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02886 | hp1 | a0002 | c0002 | t0067 | g0165 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02895 | hp1 | a0001 | c0001 | t0055 | g0001 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02895 | hp2 | a0016 | c0011 | t0013 | g0140 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0110 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0023 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02922 | hp2 | a0001 | c0001 | t0017 | g0015 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02965 | hp1 | a0002 | c0002 | t0009 | g0164 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02965 | hp2 | a0015 | c0019 | t0070 | g0266 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02970 | hp1 | a0002 | c0002 | t0013 | g0114 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02970 | hp2 | a0001 | c0001 | t0075 | g0004 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02976 | hp1 | a0004 | c0004 | t0014 | g0314 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02976 | hp2 | a0010 | c0023 | t0035 | g0061 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03017 | hp1 | a0001 | c0001 | t0048 | g0232 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0152 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03041 | hp1 | a0001 | c0001 | t0056 | g0174 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03041 | hp2 | a0002 | c0002 | t0013 | g0069 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03098 | hp1 | a0001 | c0001 | t0017 | g0021 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03098 | hp2 | a0001 | c0001 | t0022 | g0005 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03130 | hp1 | a0001 | c0007 | t0028 | g0026 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03130 | hp2 | a0001 | c0001 | t0041 | g0169 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03139 | hp1 | a0006 | c0005 | t0015 | g0006 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03139 | hp2 | a0002 | c0002 | t0009 | g0118 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03209 | hp1 | a0001 | c0024 | t0074 | g0018 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03209 | hp2 | a0004 | c0004 | t0037 | g0289 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03225 | hp1 | a0002 | c0002 | t0043 | g0040 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03225 | hp2 | a0002 | c0002 | t0013 | g0115 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03239 | hp1 | a0001 | c0029 | t0002 | g0229 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0096 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03453 | hp1 | a0001 | c0009 | t0033 | g0019 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03453 | hp2 | a0002 | c0002 | t0026 | g0046 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0119 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03486 | hp2 | a0001 | c0001 | t0034 | g0030 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03490 | hp2 | a0009 | c0014 | t0001 | g0078 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03540 | hp2 | a0002 | c0002 | t0006 | g0059 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03579 | hp1 | a0002 | c0002 | t0006 | g0037 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03579 | hp2 | a0002 | c0013 | t0071 | g0162 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03654 | hp1 | a0002 | c0002 | t0006 | g0055 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03654 | hp2 | a0004 | c0004 | t0024 | g0272 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0255 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0142 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03688 | hp1 | a0013 | c0020 | t0003 | g0265 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03688 | hp2 | a0002 | c0002 | t0072 | g0141 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03704 | hp1 | a0001 | c0001 | t0046 | g0190 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03704 | hp2 | a0002 | c0002 | t0006 | g0062 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03710 | hp1 | a0001 | c0001 | t0066 | g0102 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03710 | hp2 | a0001 | c0010 | t0002 | g0185 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03831 | hp1 | a0001 | c0001 | t0020 | g0197 | SAS | BEB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03831 | hp2 | a0003 | c0003 | t0001 | g0090 | SAS | BEB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0228 | SAS | BEB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03942 | hp2 | a0002 | c0002 | t0008 | g0126 | SAS | BEB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0089 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0279 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0278 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0222 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0263 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | YRI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18522 | hp2 | a0002 | c0002 | t0009 | g0086 | AFR | YRI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | CHB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18612 | hp2 | a0001 | c0001 | t0029 | g0269 | EAS | CHB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18906 | hp1 | a0002 | c0002 | t0026 | g0043 | AFR | YRI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18906 | hp2 | a0002 | c0002 | t0008 | g0149 | AFR | YRI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18939 | hp1 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18939 | hp2 | a0003 | c0003 | t0001 | g0093 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0144 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18943 | hp2 | a0003 | c0003 | t0001 | g0103 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18948 | hp2 | a0003 | c0003 | t0023 | g0012 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18950 | hp2 | a0003 | c0003 | t0001 | g0085 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18953 | hp1 | a0003 | c0003 | t0001 | g0088 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18956 | hp1 | a0001 | c0001 | t0011 | g0245 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18956 | hp2 | a0003 | c0003 | t0001 | g0109 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18957 | hp1 | a0003 | c0003 | t0001 | g0104 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18957 | hp2 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18959 | hp1 | a0003 | c0003 | t0023 | g0097 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0181 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18960 | hp1 | a0004 | c0004 | t0004 | g0287 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18960 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18963 | hp1 | a0004 | c0004 | t0018 | g0291 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18967 | hp1 | a0004 | c0028 | t0004 | g0282 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18967 | hp2 | a0003 | c0003 | t0008 | g0084 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18969 | hp1 | a0004 | c0004 | t0004 | g0298 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18969 | hp2 | a0001 | c0001 | t0021 | g0267 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18973 | hp1 | a0004 | c0004 | t0004 | g0292 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18973 | hp2 | a0003 | c0003 | t0001 | g0082 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18977 | hp2 | a0003 | c0003 | t0060 | g0098 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18979 | hp2 | a0002 | c0002 | t0008 | g0159 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18980 | hp1 | a0001 | c0001 | t0010 | g0203 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18980 | hp2 | a0003 | c0003 | t0001 | g0077 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18981 | hp1 | a0001 | c0001 | t0010 | g0226 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0139 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18982 | hp1 | a0001 | c0001 | t0051 | g0230 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18982 | hp2 | a0003 | c0003 | t0001 | g0087 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18983 | hp1 | a0002 | c0002 | t0061 | g0130 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18983 | hp2 | a0001 | c0001 | t0030 | g0243 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18984 | hp1 | a0003 | c0003 | t0008 | g0105 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18984 | hp2 | a0004 | c0004 | t0004 | g0295 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18985 | hp1 | a0003 | c0003 | t0073 | g0011 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18986 | hp1 | a0004 | c0004 | t0004 | g0281 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18986 | hp2 | a0001 | c0001 | t0029 | g0252 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18990 | hp2 | a0003 | c0003 | t0008 | g0075 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18991 | hp1 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18991 | hp2 | a0004 | c0004 | t0004 | g0301 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18992 | hp1 | a0004 | c0004 | t0004 | g0302 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18994 | hp2 | a0001 | c0001 | t0010 | g0227 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18997 | hp1 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18997 | hp2 | a0004 | c0004 | t0004 | g0290 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19003 | hp2 | a0003 | c0003 | t0008 | g0112 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19004 | hp2 | a0003 | c0003 | t0001 | g0121 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19005 | hp1 | a0004 | c0004 | t0036 | g0293 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19005 | hp2 | a0003 | c0003 | t0001 | g0092 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19006 | hp1 | a0001 | c0001 | t0010 | g0224 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19007 | hp2 | a0003 | c0003 | t0001 | g0091 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19009 | hp1 | a0001 | c0001 | t0052 | g0256 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19009 | hp2 | a0004 | c0004 | t0004 | g0297 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19010 | hp1 | a0004 | c0004 | t0004 | g0296 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19010 | hp2 | a0003 | c0003 | t0001 | g0106 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19012 | hp1 | a0003 | c0003 | t0001 | g0113 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19012 | hp2 | a0001 | c0001 | t0058 | g0253 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19030 | hp1 | a0004 | c0004 | t0018 | g0306 | AFR | LWK | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19030 | hp2 | a0002 | c0002 | t0009 | g0163 | AFR | LWK | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19043 | hp1 | a0011 | c0017 | t0013 | g0145 | AFR | LWK | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19043 | hp2 | a0002 | c0015 | t0006 | g0047 | AFR | LWK | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19055 | hp2 | a0004 | c0004 | t0004 | g0294 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19057 | hp2 | a0003 | c0003 | t0063 | g0071 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19058 | hp2 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19064 | hp1 | a0002 | c0002 | t0059 | g0129 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19064 | hp2 | a0004 | c0004 | t0004 | g0305 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19065 | hp1 | a0001 | c0001 | t0050 | g0221 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19070 | hp2 | a0004 | c0004 | t0004 | g0300 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19077 | hp1 | a0003 | c0003 | t0023 | g0010 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19077 | hp2 | a0001 | c0001 | t0021 | g0257 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19079 | hp2 | a0004 | c0004 | t0004 | g0304 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19081 | hp1 | a0001 | c0001 | t0011 | g0237 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19081 | hp2 | a0004 | c0004 | t0004 | g0303 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19082 | hp1 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19082 | hp2 | a0001 | c0001 | t0010 | g0264 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19083 | hp1 | a0003 | c0003 | t0062 | g0072 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19083 | hp2 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0107 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19089 | hp1 | a0003 | c0003 | t0001 | g0234 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19089 | hp2 | a0001 | c0001 | t0010 | g0238 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19090 | hp1 | a0004 | c0004 | t0018 | g0299 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19240 | hp1 | a0002 | c0002 | t0032 | g0161 | AFR | YRI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA19240 | hp2 | a0001 | c0009 | t0033 | g0020 | AFR | YRI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA20129 | hp1 | a0002 | c0002 | t0019 | g0058 | AFR | ASW | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA20129 | hp2 | a0001 | c0001 | t0017 | g0028 | AFR | ASW | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA20805 | hp1 | a0001 | c0001 | t0012 | g0196 | EUR | TSI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0153 | EUR | TSI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG01123 | hp2 | a0001 | c0001 | t0027 | g0131 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02109 | hp1 | a0001 | c0007 | t0028 | g0025 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02486 | hp1 | a0002 | c0002 | t0025 | g0036 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02486 | hp2 | a0001 | c0001 | t0016 | g0223 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02559 | hp1 | a0002 | c0002 | t0006 | g0054 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG02559 | hp2 | a0001 | c0012 | t0003 | g0280 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03471 | hp1 | a0008 | c0026 | t0039 | g0016 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG03471 | hp2 | a0002 | c0008 | t0006 | g0048 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG06807 | hp1 | a0001 | c0001 | t0044 | g0258 | AFR | USA | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0151 | AFR | USA | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA18955 | hp2 | a0004 | c0004 | t0004 | g0285 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA20300 | hp1 | a0003 | c0003 | t0065 | g0122 | AFR | USA | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA20300 | hp2 | a0001 | c0001 | t0034 | g0031 | AFR | USA | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA21309 | hp1 | a0002 | c0002 | t0069 | g0063 | AFR | LWK | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | LWK | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0016 | g0277 | REF | REF | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0156 | REF | REF | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:9221885
|
C | G | 2 | a0004a0007 | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
missense_variant | MODERATE | c.829C>G | p.Pro277Ala | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/13 | 1065/11284 | 829/6189 | 277/2062 | chr18 | 9221885 | ||
| chr18:9254391
|
T | C | 1 | a0016 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.1124T>C | p.Ile375Thr | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 1360/11284 | 1124/6189 | 375/2062 | chr18 | 9254391 | ||
| chr18:9254449
|
A | C | 1 | a0008 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1182A>C | p.Glu394Asp | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 1418/11284 | 1182/6189 | 394/2062 | chr18 | 9254449 | ||
| chr18:9254787
|
C | T | 2 | a0004a0007 | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
missense_variant | MODERATE | c.1520C>T | p.Thr507Ile | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 1756/11284 | 1520/6189 | 507/2062 | chr18 | 9254787 | ||
| chr18:9254859
|
C | G | 1 | a0005 | 5 | HG00099.hp1 HG01255.hp1 HG01256.hp1 others(2): Show |
missense_variant | MODERATE | c.1592C>G | p.Thr531Ser | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 1828/11284 | 1592/6189 | 531/2062 | chr18 | 9254859 | ||
| chr18:9255473
|
A | G | 1 | a0007 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.2206A>G | p.Thr736Ala | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2442/11284 | 2206/6189 | 736/2062 | chr18 | 9255473 | ||
| chr18:9255720
|
G | A | 2 | a0003a0009 | 45 | HG00323.hp1 HG00609.hp1 HG00621.hp1 others(42): Show |
missense_variant | MODERATE | c.2453G>A | p.Ser818Asn | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2689/11284 | 2453/6189 | 818/2062 | chr18 | 9255720 | ||
| chr18:9255786
|
C | A | 3 | a0004a0006a0007 | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
missense_variant | MODERATE | c.2519C>A | p.Thr840Asn | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2755/11284 | 2519/6189 | 840/2062 | chr18 | 9255786 | ||
| chr18:9255867
|
T | G | 1 | a0009 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.2600T>G | p.Ile867Arg | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2836/11284 | 2600/6189 | 867/2062 | chr18 | 9255867 | ||
| chr18:9255891
|
C | T | 1 | a0010 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.2624C>T | p.Ser875Leu | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2860/11284 | 2624/6189 | 875/2062 | chr18 | 9255891 | ||
| chr18:9255984
|
A | G | 6 | a0001a0005a0008others(3): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(145): Show |
missense_variant | MODERATE | c.2717A>G | p.Lys906Arg | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2953/11284 | 2717/6189 | 906/2062 | chr18 | 9255984 | ||
| chr18:9256048
|
A | C | 1 | a0006 | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
missense_variant | MODERATE | c.2781A>C | p.Glu927Asp | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 3017/11284 | 2781/6189 | 927/2062 | chr18 | 9256048 | ||
| chr18:9256232
|
G | A | 1 | a0015 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.2965G>A | p.Gly989Ser | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 3201/11284 | 2965/6189 | 989/2062 | chr18 | 9256232 | ||
| chr18:9256635
|
A | C | 1 | a0016 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.3368A>C | p.Lys1123Thr | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 3604/11284 | 3368/6189 | 1123/2062 | chr18 | 9256635 | ||
| chr18:9256857
|
C | T | 1 | a0011 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.3590C>T | p.Pro1197Leu | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 3826/11284 | 3590/6189 | 1197/2062 | chr18 | 9256857 | ||
| chr18:9257061
|
G | A | 1 | a0013 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.3794G>A | p.Ser1265Asn | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 4030/11284 | 3794/6189 | 1265/2062 | chr18 | 9257061 | ||
| chr18:9257579
|
A | G | 1 | a0014 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.4312A>G | p.Asn1438Asp | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 4548/11284 | 4312/6189 | 1438/2062 | chr18 | 9257579 | ||
| chr18:9258090
|
A | G | 1 | a0012 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.4823A>G | p.Lys1608Arg | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 5059/11284 | 4823/6189 | 1608/2062 | chr18 | 9258090 | ||
| chr18:9258539
|
T | C | 4 | a0004a0006a0007others(1): Show | 41 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(38): Show |
missense_variant | MODERATE | c.5272T>C | p.Ser1758Pro | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 5508/11284 | 5272/6189 | 1758/2062 | chr18 | 9258539 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:9204537
|
A | G | 1 | a0001c0029 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.297A>G | p.Thr99Thr | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/13 | 533/11284 | 297/6189 | 99/2062 | chr18 | 9204537 | ||
| chr18:9254722
|
C | T | 1 | a0001c0007 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.1455C>T | p.Asn485Asn | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 1691/11284 | 1455/6189 | 485/2062 | chr18 | 9254722 | ||
| chr18:9254887
|
T | G | 1 | a0002c0008 | 2 | HG01081.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.1620T>G | p.Thr540Thr | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 1856/11284 | 1620/6189 | 540/2062 | chr18 | 9254887 | ||
| chr18:9255124
|
A | G | 1 | a0004c0028 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.1857A>G | p.Lys619Lys | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2093/11284 | 1857/6189 | 619/2062 | chr18 | 9255124 | ||
| chr18:9255214
|
A | G | 1 | a0002c0025 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.1947A>G | p.Thr649Thr | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2183/11284 | 1947/6189 | 649/2062 | chr18 | 9255214 | ||
| chr18:9255304
|
G | A | 1 | a0001c0012 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.2037G>A | p.Lys679Lys | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2273/11284 | 2037/6189 | 679/2062 | chr18 | 9255304 | ||
| chr18:9255541
|
C | T | 1 | a0001c0010 | 2 | HG02683.hp2 HG03710.hp2 |
synonymous_variant | LOW | c.2274C>T | p.Ser758Ser | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2510/11284 | 2274/6189 | 758/2062 | chr18 | 9255541 | ||
| chr18:9255574
|
T | C | 1 | a0002c0013 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.2307T>C | p.Asp769Asp | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2543/11284 | 2307/6189 | 769/2062 | chr18 | 9255574 | ||
| chr18:9255577
|
A | G | 1 | a0001c0024 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.2310A>G | p.Leu770Leu | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2546/11284 | 2310/6189 | 770/2062 | chr18 | 9255577 | ||
| chr18:9255961
|
C | T | 2 | a0002c0013a0002c0022 | 2 | HG01167.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.2694C>T | p.Asp898Asp | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2930/11284 | 2694/6189 | 898/2062 | chr18 | 9255961 | ||
| chr18:9256132
|
C | T | 1 | a0002c0018 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.2865C>T | p.Asp955Asp | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 3101/11284 | 2865/6189 | 955/2062 | chr18 | 9256132 | ||
| chr18:9257153
|
C | T | 1 | a0001c0009 | 2 | HG03453.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.3886C>T | p.Leu1296Leu | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 4122/11284 | 3886/6189 | 1296/2062 | chr18 | 9257153 | ||
| chr18:9258533
|
C | T | 5 | a0004c0004a0004c0028a0006c0005others(2): Show | 41 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(38): Show |
synonymous_variant | LOW | c.5266C>T | p.Leu1756Leu | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 5502/11284 | 5266/6189 | 1756/2062 | chr18 | 9258533 | ||
| chr18:9258904
|
C | T | 2 | a0002c0008a0002c0015 | 3 | HG01081.hp2 HG03471.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.5637C>T | p.Asn1879Asn | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 5873/11284 | 5637/6189 | 1879/2062 | chr18 | 9258904 | ||
| chr18:9275544
|
C | T | 3 | a0004c0004a0004c0028a0007c0027 | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
synonymous_variant | LOW | c.5784C>T | p.Asn1928Asn | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/13 | 6020/11284 | 5784/6189 | 1928/2062 | chr18 | 9275544 | ||
| chr18:9275565
|
T | G | 3 | a0004c0004a0004c0028a0007c0027 | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
synonymous_variant | LOW | c.5805T>G | p.Val1935Val | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/13 | 6041/11284 | 5805/6189 | 1935/2062 | chr18 | 9275565 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:9281317
|
G | C | 1 | a0010c0023t0035 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 191 | chr18 | 9281317 | |||||
| chr18:9281325
|
T | A | 9 | a0004c0004t0004a0004c0004t0014a0004c0004t0018others(6): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*199T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 199 | chr18 | 9281325 | |||||
| chr18:9281550
|
G | A | 1 | a0008c0026t0039 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*424G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 424 | chr18 | 9281550 | |||||
| chr18:9281569
|
T | C | 11 | a0004c0004t0004a0004c0004t0014a0004c0004t0018others(8): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*443T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 443 | chr18 | 9281569 | |||||
| chr18:9281782
|
T | A | 1 | a0001c0001t0041 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*656T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 656 | chr18 | 9281782 | |||||
| chr18:9282144
|
T | C | 6 | a0002c0002t0006a0002c0002t0019a0002c0002t0025others(3): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1018T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 1018 | chr18 | 9282144 | |||||
| chr18:9282482
|
G | A | 1 | a0002c0018t0042 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1356G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 1356 | chr18 | 9282482 | |||||
| chr18:9282585
|
G | A | 1 | a0002c0002t0043 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1459G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 1459 | chr18 | 9282585 | |||||
| chr18:9282857
|
T | TA | 17 | a0001c0001t0002a0001c0001t0005a0001c0001t0010others(14): Show | 71 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1741dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 1742 | INFO_REALIGN_3_PRIME | chr18 | 9282857 | ||||
| chr18:9283160
|
T | G | 1 | a0001c0001t0027 | 2 | HG01123.hp2 HG01934.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2034T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2034 | chr18 | 9283160 | |||||
| chr18:9283181
|
A | G | 1 | a0002c0002t0026 | 2 | HG03453.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2055A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2055 | chr18 | 9283181 | |||||
| chr18:9283219
|
A | G | 1 | a0001c0001t0075 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2093A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2093 | chr18 | 9283219 | |||||
| chr18:9283699
|
T | C | 2 | a0001c0001t0021a0001c0001t0052 | 4 | HG02132.hp1 NA18969.hp2 NA19009.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2573T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2573 | chr18 | 9283699 | |||||
| chr18:9283785
|
C | T | 1 | a0001c0001t0034 | 2 | HG03486.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2659C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2659 | chr18 | 9283785 | |||||
| chr18:9284084
|
G | A | 2 | a0001c0007t0028a0001c0007t0053 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2958G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2958 | chr18 | 9284084 | |||||
| chr18:9284087
|
C | T | 1 | a0001c0009t0033 | 2 | HG03453.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2961C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2961 | chr18 | 9284087 | |||||
| chr18:9284202
|
A | G | 1 | a0010c0023t0035 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3076A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3076 | chr18 | 9284202 | |||||
| chr18:9284402
|
TTG | T | 9 | a0004c0004t0004a0004c0004t0014a0004c0004t0018others(6): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3278_*3279delGT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3278 | INFO_REALIGN_3_PRIME | chr18 | 9284402 | ||||
| chr18:9284428
|
A | G | 1 | a0004c0004t0038 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3302A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3302 | chr18 | 9284428 | |||||
| chr18:9284604
|
T | C | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(34): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*3478T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3478 | chr18 | 9284604 | |||||
| chr18:9284829
|
A | G | 3 | a0001c0024t0074a0002c0002t0032a0010c0023t0035 | 4 | HG01891.hp2 HG02976.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3703A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3703 | chr18 | 9284829 | |||||
| chr18:9284935
|
A | G | 1 | a0001c0001t0051 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3809A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3809 | chr18 | 9284935 | |||||
| chr18:9284943
|
G | A | 2 | a0001c0001t0020a0001c0001t0044 | 4 | HG01106.hp1 HG01433.hp1 HG03831.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3817G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3817 | chr18 | 9284943 | |||||
| chr18:9284944
|
C | T | 2 | a0001c0001t0020a0001c0001t0044 | 4 | HG01106.hp1 HG01433.hp1 HG03831.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3818C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3818 | chr18 | 9284944 | |||||
| chr18:9284953
|
T | C | 1 | a0002c0018t0042 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3827T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3827 | chr18 | 9284953 | |||||
| chr18:9284972
|
C | T | 1 | a0001c0001t0031 | 2 | HG01515.hp1 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3846C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3846 | chr18 | 9284972 | |||||
| chr18:9284973
|
A | G | 2 | a0001c0001t0031a0004c0004t0037 | 3 | HG01515.hp1 HG01515.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3847A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3847 | chr18 | 9284973 | |||||
| chr18:9284978
|
G | A | 1 | a0001c0009t0033 | 2 | HG03453.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3852G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3852 | chr18 | 9284978 | |||||
| chr18:9284988
|
C | T | 6 | a0002c0002t0006a0002c0002t0019a0002c0002t0025others(3): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3862C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3862 | chr18 | 9284988 | |||||
| chr18:9285017
|
T | C | 1 | a0002c0002t0059 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3891T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3891 | chr18 | 9285017 | |||||
| chr18:9285019
|
A | G | 1 | a0001c0001t0050 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3893A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3893 | chr18 | 9285019 | |||||
| chr18:9285030
|
C | A | 3 | a0002c0002t0013a0011c0017t0013a0016c0011t0013 | 5 | HG02895.hp2 HG02970.hp1 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3904C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3904 | chr18 | 9285030 | |||||
| chr18:9285034
|
G | A | 2 | a0004c0004t0014a0004c0004t0038 | 5 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3908G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3908 | chr18 | 9285034 | |||||
| chr18:9285125
|
C | T | 18 | a0001c0001t0002a0001c0001t0005a0001c0001t0010others(15): Show | 68 | HG01099.hp1 HG01106.hp1 HG01123.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*3999C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3999 | chr18 | 9285125 | |||||
| chr18:9285130
|
G | A | 19 | a0001c0001t0002a0001c0001t0005a0001c0001t0010others(16): Show | 69 | HG01099.hp1 HG01106.hp1 HG01123.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*4004G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4004 | chr18 | 9285130 | |||||
| chr18:9285133
|
T | C | 19 | a0001c0001t0002a0001c0001t0005a0001c0001t0010others(16): Show | 69 | HG01099.hp1 HG01106.hp1 HG01123.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*4007T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4007 | chr18 | 9285133 | |||||
| chr18:9285141
|
G | A | 2 | a0002c0002t0059a0002c0002t0061 | 2 | NA18983.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4015G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4015 | chr18 | 9285141 | |||||
| chr18:9285163
|
C | T | 1 | a0004c0004t0036 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4037C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4037 | chr18 | 9285163 | |||||
| chr18:9285165
|
T | C | 3 | a0003c0003t0062a0003c0003t0063a0004c0004t0036 | 3 | NA19005.hp1 NA19057.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4039T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4039 | chr18 | 9285165 | |||||
| chr18:9285208
|
C | CA | 8 | a0001c0001t0022a0001c0001t0046a0001c0001t0054others(5): Show | 14 | HG00140.hp1 HG00639.hp2 HG01106.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4097dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4098 | INFO_REALIGN_3_PRIME | chr18 | 9285208 | ||||
| chr18:9285220
|
AAAAG | A | 6 | a0001c0001t0011a0001c0001t0012a0001c0001t0047others(3): Show | 15 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4102_*4105delGAAA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4102 | INFO_REALIGN_3_PRIME | chr18 | 9285220 | ||||
| chr18:9285234
|
A | T | 1 | a0002c0002t0072 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4108A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4108 | chr18 | 9285234 | |||||
| chr18:9285245
|
A | G | 1 | a0002c0002t0032 | 2 | HG01891.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4119A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4119 | chr18 | 9285245 | |||||
| chr18:9285296
|
C | T | 3 | a0002c0013t0071a0006c0005t0015a0006c0005t0040 | 6 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4170C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4170 | chr18 | 9285296 | |||||
| chr18:9285302
|
C | T | 1 | a0008c0026t0039 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4176C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4176 | chr18 | 9285302 | |||||
| chr18:9285427
|
C | CA | 20 | a0001c0001t0005a0001c0001t0045a0001c0001t0046others(17): Show | 47 | HG00099.hp2 HG00639.hp2 HG01069.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*4324dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4325 | INFO_REALIGN_3_PRIME | chr18 | 9285427 | ||||
| chr18:9285427
|
C | CAA | 3 | a0001c0001t0010a0001c0001t0055a0001c0001t0066 | 8 | HG02895.hp1 HG03710.hp1 NA18980.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4323_*4324dupAA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4325 | INFO_REALIGN_3_PRIME | chr18 | 9285427 | ||||
| chr18:9285427
|
CA | C | 11 | a0001c0001t0020a0001c0001t0049a0001c0001t0057others(8): Show | 36 | HG00639.hp1 HG01106.hp1 HG01106.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*4324delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4324 | INFO_REALIGN_3_PRIME | chr18 | 9285427 | ||||
| chr18:9285428
|
A | C | 4 | a0001c0001t0017a0001c0001t0034a0001c0024t0074others(1): Show | 8 | HG02055.hp1 HG02922.hp2 HG03098.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4302A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4302 | chr18 | 9285428 | |||||
| chr18:9285511
|
C | T | 1 | a0002c0002t0032 | 2 | HG01891.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4385C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4385 | chr18 | 9285511 | |||||
| chr18:9285540
|
T | G | 1 | a0001c0001t0029 | 2 | NA18612.hp2 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4414T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4414 | chr18 | 9285540 | |||||
| chr18:9285724
|
C | G | 5 | a0002c0002t0006a0002c0002t0025a0002c0002t0026others(2): Show | 20 | HG00140.hp2 HG00733.hp2 HG01081.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4598C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4598 | chr18 | 9285724 | |||||
| chr18:9285826
|
T | C | 24 | a0001c0001t0048a0001c0009t0033a0002c0002t0006others(21): Show | 70 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*4700T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4700 | chr18 | 9285826 | |||||
| chr18:9285889
|
G | C | 1 | a0002c0002t0069 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4763G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4763 | chr18 | 9285889 | |||||
| chr18:9285894
|
T | G | 40 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(37): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*4768T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4768 | chr18 | 9285894 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:9137220
|
C | CCCGCCCG others(11): Show |
1 | a0001c0001t0031g0317 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-52+258_-52+275dup others(18): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9137220 | |||||
| chr18:9137251
|
A | G | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-52+286A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137251 | ||||||
| chr18:9137280
|
A | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-52+315A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137280 | ||||||
| chr18:9137308
|
G | A | 4 | a0001c0001t0022g0002a0001c0001t0022g0005a0001c0001t0054g0003others(1): Show | 4 | HG00639.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+343G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137308 | ||||||
| chr18:9137333
|
G | A | 4 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+368G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137333 | ||||||
| chr18:9137406
|
G | T | 34 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(31): Show | 34 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.-52+441G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137406 | ||||||
| chr18:9137456
|
G | C | 3 | a0003c0003t0023g0010a0003c0003t0023g0012a0003c0003t0073g0011 | 3 | NA18948.hp2 NA18985.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-52+491G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137456 | ||||||
| chr18:9137507
|
G | T | 1 | a0001c0012t0003g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-52+542G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137507 | ||||||
| chr18:9137518
|
C | T | 5 | a0004c0004t0014g0311a0004c0004t0014g0312a0004c0004t0014g0313others(2): Show | 5 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+553C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137518 | ||||||
| chr18:9137564
|
G | T | 1 | a0007c0027t0004g0309 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-52+599G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137564 | ||||||
| chr18:9137583
|
G | T | 121 | a0001c0001t0002g0188a0001c0001t0002g0194a0001c0001t0002g0195others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-52+618G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137583 | ||||||
| chr18:9137612
|
G | A | 1 | a0002c0002t0001g0013 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-52+647G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137612 | ||||||
| chr18:9137612
|
G | C | 1 | a0003c0003t0001g0014 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-52+647G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137612 | ||||||
| chr18:9137620
|
T | G | 203 | a0001c0001t0002g0188a0001c0001t0002g0194a0001c0001t0002g0195others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.-52+655T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137620 | ||||||
| chr18:9137808
|
A | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+843A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137808 | ||||||
| chr18:9137843
|
C | G | 1 | a0002c0002t0006g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-52+878C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137843 | ||||||
| chr18:9137858
|
A | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+893A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137858 | ||||||
| chr18:9137866
|
A | G | 1 | a0002c0002t0006g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-52+901A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137866 | ||||||
| chr18:9137952
|
G | C | 1 | a0002c0002t0069g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-52+987G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137952 | ||||||
| chr18:9138092
|
A | G | 1 | a0004c0004t0004g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-52+1127A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138092 | ||||||
| chr18:9138121
|
G | T | 1 | a0004c0004t0024g0307 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-52+1156G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138121 | ||||||
| chr18:9138222
|
CAT | C | 3 | a0002c0002t0009g0163a0002c0002t0009g0164a0002c0002t0067g0165 | 3 | HG02886.hp1 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-52+1260_-52+1261d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9138222 | |||||
| chr18:9138247
|
T | G | 139 | a0001c0001t0002g0064a0001c0001t0002g0188a0001c0001t0002g0194others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-52+1282T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138247 | ||||||
| chr18:9138324
|
C | A | 1 | a0001c0001t0027g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-52+1359C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138324 | ||||||
| chr18:9138360
|
A | G | 2 | a0001c0001t0002g0278a0001c0001t0003g0279 | 2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-52+1395A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138360 | ||||||
| chr18:9138372
|
G | C | 139 | a0001c0001t0002g0064a0001c0001t0002g0188a0001c0001t0002g0194others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-52+1407G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138372 | ||||||
| chr18:9138408
|
G | A | 1 | a0001c0001t0005g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-52+1443G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138408 | ||||||
| chr18:9138481
|
C | G | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-52+1516C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138481 | ||||||
| chr18:9138525
|
AAAAC | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+1580_-52+1583d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9138525 | |||||
| chr18:9138549
|
A | C | 1 | a0004c0004t0018g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-52+1584A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138549 | ||||||
| chr18:9138663
|
A | G | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+1698A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138663 | ||||||
| chr18:9138684
|
A | G | 1 | a0007c0027t0004g0309 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-52+1719A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138684 | ||||||
| chr18:9138841
|
T | C | 4 | a0001c0001t0003g0001a0001c0001t0041g0169a0001c0001t0055g0001others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+1876T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138841 | ||||||
| chr18:9138996
|
C | T | 1 | a0001c0001t0003g0279 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-52+2031C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138996 | ||||||
| chr18:9139101
|
A | T | 3 | a0001c0001t0017g0029a0001c0001t0034g0030a0001c0001t0034g0031 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-52+2136A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139101 | ||||||
| chr18:9139159
|
A | G | 1 | a0001c0001t0016g0277 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-52+2194A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139159 | ||||||
| chr18:9139210
|
C | CGT | 3 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0025g0036 | 3 | HG01243.hp1 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-52+2245_-52+2246i others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139210 | ||||||
| chr18:9139211
|
T | C | 3 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0025g0036 | 3 | HG01243.hp1 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-52+2246T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139211 | ||||||
| chr18:9139248
|
C | T | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+2283C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139248 | ||||||
| chr18:9139358
|
A | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+2393A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139358 | ||||||
| chr18:9139445
|
A | T | 2 | a0001c0001t0003g0275a0001c0001t0030g0276 | 2 | HG01081.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-52+2480A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139445 | ||||||
| chr18:9139534
|
T | C | 3 | a0001c0001t0017g0029a0001c0001t0034g0030a0001c0001t0034g0031 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-52+2569T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139534 | ||||||
| chr18:9139592
|
G | A | 1 | a0004c0004t0004g0281 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-52+2627G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139592 | ||||||
| chr18:9139605
|
C | G | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-52+2640C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139605 | ||||||
| chr18:9139607
|
C | T | 4 | a0002c0002t0001g0013a0002c0002t0001g0157a0002c0002t0001g0158others(1): Show | 4 | NA18941.hp1 NA18971.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+2642C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139607 | ||||||
| chr18:9139613
|
A | G | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | NA18941.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-52+2648A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139613 | ||||||
| chr18:9139841
|
C | A | 1 | a0002c0002t0006g0039 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-52+2876C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139841 | ||||||
| chr18:9139922
|
C | A | 1 | a0001c0001t0017g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-52+2957C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139922 | ||||||
| chr18:9139966
|
C | T | 1 | a0003c0003t0023g0012 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-52+3001C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139966 | ||||||
| chr18:9140331
|
T | C | 3 | a0001c0001t0003g0172a0001c0001t0011g0171a0001c0001t0022g0170 | 3 | HG01361.hp2 HG01952.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-52+3366T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9140331 | ||||||
| chr18:9140479
|
T | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+3514T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9140479 | ||||||
| chr18:9140837
|
A | AATC | 42 | a0001c0001t0003g0271a0001c0001t0022g0005a0004c0004t0004g0281others(39): Show | 42 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.-52+3875_-52+3877d others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9140837 | |||||
| chr18:9140953
|
G | C | 316 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-52+3988G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9140953 | ||||||
| chr18:9141025
|
G | A | 3 | a0001c0001t0003g0173a0001c0001t0056g0174a0001c0012t0003g0280 | 3 | HG02559.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52+4060G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141025 | ||||||
| chr18:9141042
|
T | C | 1 | a0001c0010t0002g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-52+4077T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141042 | ||||||
| chr18:9141065
|
C | T | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0002c0002t0001g0154 | 3 | HG01099.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-52+4100C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141065 | ||||||
| chr18:9141215
|
TGTG | T | 215 | a0001c0001t0002g0188a0001c0001t0002g0194a0001c0001t0002g0195others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-52+4268_-52+4270d others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9141215 | |||||
| chr18:9141406
|
G | A | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-52+4441G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141406 | ||||||
| chr18:9141464
|
G | T | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-52+4499G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141464 | ||||||
| chr18:9141475
|
C | T | 1 | a0005c0006t0007g0270 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-52+4510C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141475 | ||||||
| chr18:9141815
|
T | C | 5 | a0001c0001t0016g0177a0005c0006t0007g0176a0005c0006t0007g0178others(2): Show | 5 | HG00099.hp1 HG01255.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+4850T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141815 | ||||||
| chr18:9141956
|
A | G | 1 | a0001c0001t0017g0028 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-52+4991A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141956 | ||||||
| chr18:9141992
|
C | T | 5 | a0001c0001t0003g0173a0001c0001t0034g0030a0001c0001t0034g0031others(2): Show | 5 | HG02559.hp2 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+5027C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141992 | ||||||
| chr18:9142033
|
A | G | 1 | a0001c0001t0029g0269 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-52+5068A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142033 | ||||||
| chr18:9142137
|
C | T | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-52+5172C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142137 | ||||||
| chr18:9142200
|
C | G | 2 | a0002c0002t0001g0150a0002c0002t0001g0151 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-52+5235C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142200 | ||||||
| chr18:9142213
|
A | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-52+5248A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142213 | ||||||
| chr18:9142232
|
C | G | 1 | a0003c0003t0001g0146 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-52+5267C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142232 | ||||||
| chr18:9142317
|
G | T | 1 | a0001c0001t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-52+5352G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142317 | ||||||
| chr18:9142522
|
C | CT | 25 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0006g0037others(22): Show | 25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-52+5558dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9142522 | |||||
| chr18:9142717
|
A | G | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+5752A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142717 | ||||||
| chr18:9142723
|
G | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+5758G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142723 | ||||||
| chr18:9142736
|
T | C | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+5771T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142736 | ||||||
| chr18:9142745
|
G | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+5780G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142745 | ||||||
| chr18:9142753
|
G | A | 120 | a0001c0001t0002g0188a0001c0001t0002g0194a0001c0001t0002g0195others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-52+5788G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142753 | ||||||
| chr18:9142882
|
CA | C | 212 | a0001c0001t0002g0188a0001c0001t0002g0194a0001c0001t0002g0195others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-52+5928delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9142882 | |||||
| chr18:9143268
|
T | C | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+6303T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143268 | ||||||
| chr18:9143396
|
C | G | 2 | a0002c0002t0043g0040a0010c0023t0035g0061 | 2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-52+6431C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143396 | ||||||
| chr18:9143444
|
A | C | 1 | a0011c0017t0013g0145 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-52+6479A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143444 | ||||||
| chr18:9143708
|
C | G | 1 | a0003c0003t0001g0144 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-52+6743C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143708 | ||||||
| chr18:9143776
|
C | T | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+6811C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143776 | ||||||
| chr18:9143799
|
C | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+6834C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143799 | ||||||
| chr18:9143813
|
G | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+6848G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143813 | ||||||
| chr18:9143822
|
AGT | A | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+6862_-52+6863d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9143822 | |||||
| chr18:9143916
|
C | G | 1 | a0002c0002t0025g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-52+6951C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143916 | ||||||
| chr18:9143944
|
A | G | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-52+6979A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143944 | ||||||
| chr18:9144223
|
G | A | 1 | a0001c0001t0005g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-52+7258G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144223 | ||||||
| chr18:9144298
|
T | G | 1 | a0001c0001t0049g0180 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-52+7333T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144298 | ||||||
| chr18:9144352
|
C | A | 1 | a0001c0001t0005g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-52+7387C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144352 | ||||||
| chr18:9144421
|
A | G | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-52+7456A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144421 | ||||||
| chr18:9144490
|
T | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+7525T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144490 | ||||||
| chr18:9144571
|
C | T | 1 | a0003c0003t0001g0014 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-52+7606C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144571 | ||||||
| chr18:9144871
|
A | T | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+7906A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144871 | ||||||
| chr18:9144877
|
TTGTA | T | 4 | a0001c0001t0020g0182a0001c0001t0020g0183a0003c0003t0001g0066others(1): Show | 4 | HG01106.hp1 HG01361.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+7921_-52+7924d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9144877 | |||||
| chr18:9144883
|
G | A | 2 | a0005c0006t0007g0176a0005c0006t0007g0270 | 2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-52+7918G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144883 | ||||||
| chr18:9144980
|
GT | G | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0002c0002t0001g0154 | 3 | HG01099.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-52+8016delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144980 | ||||||
| chr18:9145080
|
A | G | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+8115A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145080 | ||||||
| chr18:9145091
|
A | G | 1 | a0003c0003t0073g0011 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-52+8126A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145091 | ||||||
| chr18:9145169
|
C | T | 2 | a0001c0001t0054g0003a0001c0001t0075g0004 | 2 | HG00639.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-52+8204C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145169 | ||||||
| chr18:9145262
|
G | A | 1 | a0001c0024t0074g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-52+8297G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145262 | ||||||
| chr18:9145440
|
A | C | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-52+8475A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145440 | ||||||
| chr18:9145527
|
G | C | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+8562G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145527 | ||||||
| chr18:9145584
|
A | G | 1 | a0002c0002t0006g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-52+8619A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145584 | ||||||
| chr18:9145585
|
C | T | 3 | a0002c0002t0001g0150a0002c0002t0001g0151a0002c0002t0008g0149 | 3 | HG02258.hp2 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-52+8620C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145585 | ||||||
| chr18:9145586
|
G | A | 1 | a0004c0004t0038g0310 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-52+8621G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145586 | ||||||
| chr18:9145624
|
A | AATC | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-52+8661_-52+8663d others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9145624 | |||||
| chr18:9145778
|
T | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+8813T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145778 | ||||||
| chr18:9145923
|
G | T | 1 | a0001c0001t0002g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-52+8958G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145923 | ||||||
| chr18:9146872
|
A | G | 1 | a0002c0002t0008g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-52+9907A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9146872 | ||||||
| chr18:9146978
|
C | T | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+10013C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9146978 | ||||||
| chr18:9146979
|
G | A | 2 | a0001c0001t0016g0184a0001c0001t0016g0277 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-52+10014G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9146979 | ||||||
| chr18:9147314
|
G | A | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-52+10349G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147314 | ||||||
| chr18:9147546
|
T | A | 1 | a0001c0010t0002g0185 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-52+10581T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147546 | ||||||
| chr18:9147622
|
C | T | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+10657C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147622 | ||||||
| chr18:9147637
|
G | C | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+10672G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147637 | ||||||
| chr18:9147721
|
A | G | 1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-52+10756A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147721 | ||||||
| chr18:9147800
|
C | T | 1 | a0001c0001t0020g0183 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-52+10835C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147800 | ||||||
| chr18:9147914
|
A | G | 3 | a0002c0002t0001g0142a0002c0002t0068g0143a0002c0002t0072g0141 | 3 | HG00735.hp2 HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-52+10949A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147914 | ||||||
| chr18:9147966
|
A | G | 1 | a0001c0001t0021g0267 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-52+11001A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147966 | ||||||
| chr18:9148166
|
T | C | 138 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-52+11201T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148166 | ||||||
| chr18:9148323
|
T | C | 1 | a0002c0002t0013g0069 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-52+11358T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148323 | ||||||
| chr18:9148333
|
C | CAT | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+11368_-52+1136 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148333 | ||||||
| chr18:9148417
|
A | G | 1 | a0016c0011t0013g0140 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-52+11452A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148417 | ||||||
| chr18:9148631
|
C | T | 1 | a0015c0019t0070g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-52+11666C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148631 | ||||||
| chr18:9148668
|
C | T | 1 | a0001c0001t0017g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-52+11703C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148668 | ||||||
| chr18:9148674
|
C | T | 1 | a0001c0001t0002g0274 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-52+11709C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148674 | ||||||
| chr18:9148863
|
A | T | 140 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-52+11898A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148863 | ||||||
| chr18:9148912
|
A | AT | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+11951dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9148912 | |||||
| chr18:9148954
|
T | C | 1 | a0001c0001t0005g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-52+11989T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148954 | ||||||
| chr18:9149109
|
G | A | 1 | a0001c0001t0005g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-52+12144G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149109 | ||||||
| chr18:9149176
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+12211T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149176 | ||||||
| chr18:9149415
|
G | A | 2 | a0002c0002t0043g0040a0010c0023t0035g0061 | 2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-52+12450G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149415 | ||||||
| chr18:9149417
|
A | G | 25 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0006g0037others(22): Show | 25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-52+12452A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149417 | ||||||
| chr18:9149439
|
A | T | 140 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-52+12474A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149439 | ||||||
| chr18:9149515
|
G | A | 1 | a0002c0002t0001g0070 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-52+12550G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149515 | ||||||
| chr18:9149636
|
G | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+12671G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149636 | ||||||
| chr18:9149719
|
A | G | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-52+12754A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149719 | ||||||
| chr18:9149771
|
G | GATTT | 159 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.-52+12822_-52+1282 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9149771 | |||||
| chr18:9149771
|
G | GATTTATT others(5): Show |
5 | a0004c0004t0014g0311a0004c0004t0014g0312a0004c0004t0014g0313others(2): Show | 5 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+12814_-52+1282 others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9149771 | |||||
| chr18:9149788
|
A | ATTTAT | 4 | a0004c0004t0004g0283a0004c0004t0004g0284a0004c0004t0004g0285others(1): Show | 4 | HG02015.hp1 HG02135.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+12825_-52+1282 others(9): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9149788 | |||||
| chr18:9149791
|
A | T | 208 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-52+12826A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149791 | ||||||
| chr18:9149792
|
A | ATTT | 34 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0005g0167others(31): Show | 34 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-52+12827_-52+1282 others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149792 | ||||||
| chr18:9149792
|
A | ATTTT | 5 | a0004c0004t0004g0281a0004c0004t0004g0304a0004c0004t0004g0305others(2): Show | 5 | HG00639.hp1 HG02809.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+12827_-52+1282 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149792 | ||||||
| chr18:9149792
|
A | C | 3 | a0004c0004t0004g0283a0004c0004t0004g0284a0004c0004t0004g0285 | 3 | HG02015.hp1 HG02135.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-52+12827A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149792 | ||||||
| chr18:9149792
|
A | T | 1 | a0004c0004t0018g0299 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-52+12827A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149792 | ||||||
| chr18:9149793
|
A | T | 178 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-52+12828A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149793 | ||||||
| chr18:9149796
|
T | TA | 5 | a0004c0004t0004g0286a0004c0004t0004g0287a0004c0004t0004g0288others(2): Show | 5 | HG01934.hp2 HG02132.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+12831_-52+1283 others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149796 | ||||||
| chr18:9149796
|
T | TTTTA | 3 | a0004c0004t0004g0301a0004c0004t0004g0302a0004c0004t0004g0303 | 3 | NA18991.hp2 NA18992.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-52+12832_-52+1283 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9149796 | |||||
| chr18:9149797
|
T | TTA | 27 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0005g0167others(24): Show | 27 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-52+12832_-52+1283 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149797 | ||||||
| chr18:9149798
|
A | T | 55 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0005g0167others(52): Show | 55 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-52+12833A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149798 | ||||||
| chr18:9149799
|
T | A | 1 | a0001c0001t0007g0189 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-52+12834T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149799 | ||||||
| chr18:9149801
|
T | A | 1 | a0001c0001t0007g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-52+12836T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149801 | ||||||
| chr18:9149802
|
T | A | 4 | a0002c0002t0009g0163a0002c0002t0009g0164a0004c0004t0014g0311others(1): Show | 4 | HG02723.hp1 HG02965.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+12837T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149802 | ||||||
| chr18:9149804
|
T | A | 4 | a0001c0001t0002g0188a0001c0001t0002g0273a0001c0001t0002g0274others(1): Show | 4 | HG03486.hp2 NA18612.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+12839T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149804 | ||||||
| chr18:9149806
|
T | A | 2 | a0004c0004t0024g0272a0004c0004t0024g0307 | 2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-52+12841T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149806 | ||||||
| chr18:9149953
|
C | T | 3 | a0002c0002t0001g0137a0003c0003t0001g0138a0003c0003t0001g0139 | 3 | HG00609.hp1 NA18981.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-52+12988C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149953 | ||||||
| chr18:9150017
|
G | C | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-52+13052G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150017 | ||||||
| chr18:9150091
|
G | A | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-52+13126G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150091 | ||||||
| chr18:9150143
|
T | A | 216 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.-52+13178T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150143 | ||||||
| chr18:9150153
|
G | C | 1 | a0001c0001t0002g0188 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-52+13188G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150153 | ||||||
| chr18:9150235
|
C | A | 3 | a0001c0001t0017g0029a0001c0001t0034g0030a0001c0001t0034g0031 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-52+13270C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150235 | ||||||
| chr18:9150497
|
A | G | 1 | a0001c0001t0003g0263 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-52+13532A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150497 | ||||||
| chr18:9150637
|
T | A | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+13672T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150637 | ||||||
| chr18:9150638
|
T | A | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162others(1): Show | 4 | HG01167.hp1 HG01891.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+13673T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150638 | ||||||
| chr18:9150639
|
A | T | 19 | a0001c0001t0027g0065a0001c0001t0027g0131a0002c0002t0001g0013others(16): Show | 19 | HG00423.hp1 HG01123.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.-52+13674A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150639 | ||||||
| chr18:9150656
|
T | A | 1 | a0001c0001t0046g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-52+13691T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150656 | ||||||
| chr18:9150740
|
G | A | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162others(1): Show | 4 | HG01167.hp1 HG01891.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+13775G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150740 | ||||||
| chr18:9150754
|
G | A | 220 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.-52+13789G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150754 | ||||||
| chr18:9150897
|
C | T | 1 | a0003c0003t0065g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-52+13932C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150897 | ||||||
| chr18:9150920
|
T | A | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-52+13955T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150920 | ||||||
| chr18:9150964
|
T | TA | 148 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.-52+14009dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9150964 | |||||
| chr18:9151030
|
A | G | 2 | a0002c0002t0043g0040a0010c0023t0035g0061 | 2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-52+14065A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151030 | ||||||
| chr18:9151092
|
A | C | 1 | a0001c0001t0075g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-52+14127A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151092 | ||||||
| chr18:9151211
|
C | T | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+14246C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151211 | ||||||
| chr18:9151277
|
G | A | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+14312G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151277 | ||||||
| chr18:9151316
|
A | G | 1 | a0004c0004t0037g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-52+14351A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151316 | ||||||
| chr18:9151351
|
A | G | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-52+14386A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151351 | ||||||
| chr18:9151465
|
T | C | 1 | a0001c0001t0021g0191 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-52+14500T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151465 | ||||||
| chr18:9151493
|
G | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+14528G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151493 | ||||||
| chr18:9151624
|
C | G | 131 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0188others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.-52+14659C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151624 | ||||||
| chr18:9151683
|
C | G | 1 | a0004c0004t0004g0300 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-52+14718C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151683 | ||||||
| chr18:9151714
|
G | A | 3 | a0001c0001t0003g0173a0001c0001t0056g0174a0001c0012t0003g0280 | 3 | HG02559.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52+14749G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151714 | ||||||
| chr18:9151983
|
G | A | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | NA18955.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-52+15018G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151983 | ||||||
| chr18:9152086
|
A | G | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+15121A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152086 | ||||||
| chr18:9152117
|
A | G | 1 | a0001c0001t0034g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-52+15152A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152117 | ||||||
| chr18:9152579
|
A | G | 1 | a0003c0003t0001g0121 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-52+15614A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152579 | ||||||
| chr18:9152636
|
C | T | 140 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-52+15671C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152636 | ||||||
| chr18:9152664
|
A | T | 2 | a0002c0002t0001g0119a0002c0025t0001g0120 | 2 | HG01167.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-52+15699A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152664 | ||||||
| chr18:9152695
|
A | G | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-52+15730A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152695 | ||||||
| chr18:9152716
|
C | T | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+15751C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152716 | ||||||
| chr18:9152748
|
A | G | 2 | a0002c0002t0001g0135a0002c0002t0001g0136 | 2 | HG02129.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-52+15783A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152748 | ||||||
| chr18:9152848
|
C | T | 12 | a0002c0002t0001g0116a0002c0002t0001g0117a0002c0002t0001g0119others(9): Show | 12 | HG01167.hp2 HG01891.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-52+15883C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152848 | ||||||
| chr18:9152877
|
T | A | 25 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0006g0037others(22): Show | 25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-52+15912T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152877 | ||||||
| chr18:9152948
|
A | ATAAACTC others(316): Show |
3 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0005g0017 | 3 | HG03490.hp1 NA19058.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-52+15996_-52+1599 others(327): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9152948 | |||||
| chr18:9152948
|
A | ATAAACTC others(317): Show |
1 | a0001c0001t0005g0262 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-52+15996_-52+1599 others(328): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9152948 | |||||
| chr18:9152958
|
T | A | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+15993T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152958 | ||||||
| chr18:9153195
|
A | G | 2 | a0001c0001t0003g0259a0001c0001t0003g0263 | 2 | HG00735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-52+16230A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9153195 | ||||||
| chr18:9153237
|
G | A | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+16272G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9153237 | ||||||
| chr18:9153542
|
A | G | 4 | a0004c0004t0014g0311a0004c0004t0014g0313a0004c0004t0014g0314others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+16577A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9153542 | ||||||
| chr18:9153714
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+16749T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9153714 | ||||||
| chr18:9153787
|
G | T | 26 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(23): Show | 26 | HG00639.hp1 HG01934.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.-52+16822G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9153787 | ||||||
| chr18:9154215
|
A | G | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+17250A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154215 | ||||||
| chr18:9154241
|
G | A | 1 | a0001c0001t0012g0192 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-52+17276G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154241 | ||||||
| chr18:9154275
|
A | G | 2 | a0001c0001t0017g0021a0001c0001t0017g0028 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-52+17310A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154275 | ||||||
| chr18:9154363
|
G | A | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+17398G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154363 | ||||||
| chr18:9154572
|
A | C | 1 | a0002c0002t0025g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-52+17607A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154572 | ||||||
| chr18:9154682
|
AGAGAT | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+17720_-52+1772 others(9): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9154682 | |||||
| chr18:9154777
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+17812T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154777 | ||||||
| chr18:9154822
|
G | A | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-52+17857G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154822 | ||||||
| chr18:9155098
|
A | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+18133A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155098 | ||||||
| chr18:9155148
|
C | T | 1 | a0001c0024t0074g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-52+18183C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155148 | ||||||
| chr18:9155344
|
C | T | 1 | a0001c0001t0044g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-52+18379C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155344 | ||||||
| chr18:9155515
|
G | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+18550G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155515 | ||||||
| chr18:9155529
|
G | A | 139 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0188others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-52+18564G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155529 | ||||||
| chr18:9155668
|
T | C | 1 | a0002c0002t0001g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-52+18703T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155668 | ||||||
| chr18:9155675
|
T | C | 7 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0006g0041others(4): Show | 7 | HG02109.hp2 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52+18710T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155675 | ||||||
| chr18:9156119
|
C | G | 1 | a0001c0001t0049g0180 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-52+19154C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156119 | ||||||
| chr18:9156137
|
C | CA | 67 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0009t0033g0019others(64): Show | 67 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.-52+19190dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9156137 | |||||
| chr18:9156137
|
C | CAA | 6 | a0001c0001t0009g0023a0002c0018t0042g0315a0004c0004t0018g0299others(3): Show | 6 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+19189_-52+1919 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9156137 | |||||
| chr18:9156137
|
C | CAAA | 124 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0188others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-52+19188_-52+1919 others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9156137 | |||||
| chr18:9156137
|
C | CAAAA | 12 | a0001c0001t0003g0173a0001c0001t0003g0193a0001c0001t0003g0263others(9): Show | 12 | HG01106.hp1 HG01123.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.-52+19187_-52+1919 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9156137 | |||||
| chr18:9156160
|
A | G | 1 | a0001c0010t0002g0185 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-52+19195A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156160 | ||||||
| chr18:9156205
|
C | A | 5 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162others(2): Show | 5 | HG01106.hp2 HG01167.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+19240C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156205 | ||||||
| chr18:9156316
|
T | C | 1 | a0001c0001t0010g0264 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-52+19351T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156316 | ||||||
| chr18:9156319
|
A | G | 1 | a0001c0001t0002g0278 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-52+19354A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156319 | ||||||
| chr18:9156344
|
T | C | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | NA18977.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-52+19379T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156344 | ||||||
| chr18:9156352
|
G | A | 62 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0188others(59): Show | 62 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.-52+19387G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156352 | ||||||
| chr18:9156534
|
G | A | 3 | a0002c0002t0001g0070a0002c0002t0001g0080a0012c0016t0001g0079 | 3 | HG01109.hp1 HG01168.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-52+19569G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156534 | ||||||
| chr18:9156600
|
A | G | 2 | a0003c0003t0001g0113a0003c0003t0008g0112 | 2 | NA19003.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-52+19635A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156600 | ||||||
| chr18:9156685
|
A | G | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+19720A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156685 | ||||||
| chr18:9156748
|
C | T | 6 | a0002c0002t0006g0053a0002c0002t0006g0054a0002c0002t0006g0055others(3): Show | 6 | HG00140.hp2 HG01070.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+19783C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156748 | ||||||
| chr18:9156926
|
T | TAGAGTAG others(14): Show |
1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-52+19963_-52+1998 others(25): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9156926 | |||||
| chr18:9156932
|
A | G | 1 | a0002c0002t0008g0134 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-52+19967A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156932 | ||||||
| chr18:9156973
|
G | A | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-52+20008G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156973 | ||||||
| chr18:9157141
|
A | G | 123 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0188others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.-52+20176A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157141 | ||||||
| chr18:9157159
|
A | G | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-52+20194A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157159 | ||||||
| chr18:9157241
|
T | TA | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-52+20277dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157241 | |||||
| chr18:9157255
|
G | A | 1 | a0001c0001t0005g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-52+20290G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157255 | ||||||
| chr18:9157426
|
T | C | 1 | a0002c0002t0001g0157 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-52+20461T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157426 | ||||||
| chr18:9157437
|
C | T | 7 | a0002c0002t0001g0116a0002c0002t0001g0117a0002c0002t0001g0119others(4): Show | 7 | HG01167.hp2 HG01891.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52+20472C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157437 | ||||||
| chr18:9157480
|
C | T | 2 | a0001c0001t0009g0022a0001c0001t0009g0023 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-52+20515C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157480 | ||||||
| chr18:9157550
|
G | GGT | 4 | a0003c0003t0001g0103a0003c0003t0001g0104a0003c0003t0008g0105others(1): Show | 4 | NA18943.hp2 NA18957.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+20620_-52+2062 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | |||||
| chr18:9157550
|
G | GGTGT | 3 | a0003c0003t0001g0014a0003c0003t0001g0138a0003c0003t0001g0139 | 3 | HG00609.hp1 NA18960.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.-52+20618_-52+2062 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | |||||
| chr18:9157550
|
G | GGTGTGT | 3 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109 | 3 | HG00621.hp1 NA18956.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-52+20616_-52+2062 others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | |||||
| chr18:9157550
|
G | GGTGTGTA others(3): Show |
2 | a0001c0001t0017g0015a0008c0026t0039g0016 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-52+20591_-52+2059 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | |||||
| chr18:9157550
|
G | GGTGTGTA others(7): Show |
2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-52+20591_-52+2059 others(18): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | |||||
| chr18:9157550
|
G | GGTGTGTA others(7): Show |
4 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+20591_-52+2059 others(18): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | |||||
| chr18:9157550
|
G | GGTGTGTA others(9): Show |
1 | a0001c0001t0017g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-52+20591_-52+2059 others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | |||||
| chr18:9157550
|
G | GGTGTGTA others(39): Show |
1 | a0001c0007t0028g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-52+20591_-52+2059 others(50): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | |||||
| chr18:9157550
|
G | GGTGTGTA others(41): Show |
1 | a0001c0007t0028g0026 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+20591_-52+2059 others(52): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | |||||
| chr18:9157550
|
G | GGTGTGTA others(45): Show |
1 | a0001c0007t0053g0027 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-52+20591_-52+2059 others(56): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | |||||
| chr18:9157550
|
G | T | 1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-52+20585G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157550 | ||||||
| chr18:9157550
|
GGT | G | 3 | a0001c0001t0005g0181a0002c0002t0001g0013a0002c0002t0001g0158 | 3 | NA18941.hp1 NA18959.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-52+20620_-52+2062 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | |||||
| chr18:9157551
|
G | GTGTGTAT others(5): Show |
20 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0006g0037others(17): Show | 20 | HG00733.hp2 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.-52+20591_-52+2059 others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157551 | |||||
| chr18:9157552
|
T | G | 1 | a0004c0004t0018g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-52+20587T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157552 | ||||||
| chr18:9157553
|
G | GTGTATGT others(3): Show |
5 | a0002c0002t0006g0053a0002c0002t0006g0059a0002c0008t0006g0048others(2): Show | 5 | HG00140.hp2 HG01081.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+20591_-52+2059 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157553 | |||||
| chr18:9157555
|
G | GTATGTGT others(9): Show |
1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-52+20591_-52+2059 others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157555 | |||||
| chr18:9157557
|
G | A | 133 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0188others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-52+20592G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157557 | ||||||
| chr18:9157559
|
G | A | 1 | a0001c0001t0003g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-52+20594G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157559 | ||||||
| chr18:9157571
|
G | A | 6 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+20606G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157571 | ||||||
| chr18:9157575
|
G | GTATATAT others(9): Show |
2 | a0004c0004t0004g0283a0004c0004t0004g0284 | 2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-52+20611_-52+2061 others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157575 | |||||
| chr18:9157577
|
G | A | 2 | a0004c0004t0004g0283a0004c0004t0004g0284 | 2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-52+20612G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157577 | ||||||
| chr18:9157577
|
G | GTATATAT others(3): Show |
1 | a0004c0004t0024g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-52+20613_-52+2061 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157577 | |||||
| chr18:9157577
|
G | GTATATAT others(5): Show |
1 | a0004c0004t0024g0307 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-52+20613_-52+2061 others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157577 | |||||
| chr18:9157577
|
G | GTATATAT others(11): Show |
1 | a0004c0004t0004g0286 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-52+20613_-52+2061 others(22): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157577 | |||||
| chr18:9157579
|
G | A | 5 | a0004c0004t0004g0283a0004c0004t0004g0284a0004c0004t0004g0286others(2): Show | 5 | HG00140.hp1 HG01934.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+20614G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157579 | ||||||
| chr18:9157579
|
G | GTATATAT others(3): Show |
1 | a0004c0004t0018g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-52+20615_-52+2061 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | |||||
| chr18:9157579
|
G | GTATATAT others(5): Show |
4 | a0004c0004t0014g0311a0004c0004t0014g0312a0004c0004t0014g0313others(1): Show | 4 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+20615_-52+2061 others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | |||||
| chr18:9157579
|
G | GTATATAT others(11): Show |
2 | a0004c0004t0004g0285a0004c0004t0004g0300 | 2 | NA18955.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-52+20615_-52+2061 others(22): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | |||||
| chr18:9157579
|
G | GTATATAT others(13): Show |
6 | a0004c0004t0004g0294a0004c0004t0004g0295a0004c0004t0004g0296others(3): Show | 6 | HG00639.hp1 NA18969.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+20615_-52+2061 others(24): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | |||||
| chr18:9157579
|
G | GTATATAT others(15): Show |
2 | a0004c0004t0004g0303a0004c0004t0036g0293 | 2 | NA19005.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-52+20615_-52+2061 others(26): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | |||||
| chr18:9157579
|
G | GTATATAT others(17): Show |
1 | a0004c0004t0004g0281 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-52+20615_-52+2061 others(28): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | |||||
| chr18:9157579
|
G | GTATATAT others(19): Show |
4 | a0004c0004t0004g0292a0004c0004t0004g0301a0004c0004t0004g0302others(1): Show | 4 | NA18973.hp1 NA18991.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+20615_-52+2061 others(30): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | |||||
| chr18:9157579
|
G | GTATATAT others(21): Show |
1 | a0004c0004t0018g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-52+20615_-52+2061 others(32): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | |||||
| chr18:9157581
|
G | A | 27 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(24): Show | 27 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.-52+20616G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157581 | ||||||
| chr18:9157581
|
G | GTATATAT others(5): Show |
1 | a0004c0004t0004g0305 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-52+20617_-52+2061 others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157581 | |||||
| chr18:9157581
|
G | GTATATAT others(7): Show |
1 | a0004c0004t0014g0314 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-52+20617_-52+2061 others(18): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157581 | |||||
| chr18:9157581
|
G | GTATATAT others(9): Show |
1 | a0004c0004t0037g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-52+20617_-52+2061 others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157581 | |||||
| chr18:9157581
|
G | GTATATAT others(11): Show |
1 | a0004c0004t0004g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-52+20617_-52+2061 others(22): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157581 | |||||
| chr18:9157581
|
G | GTATATAT others(19): Show |
1 | a0004c0004t0004g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-52+20617_-52+2061 others(30): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157581 | |||||
| chr18:9157583
|
G | A | 144 | a0001c0001t0002g0188a0001c0001t0002g0194a0001c0001t0002g0195others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-52+20618G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157583 | ||||||
| chr18:9157583
|
G | GTATATAT others(7): Show |
1 | a0001c0001t0017g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-52+20619_-52+2062 others(18): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157583 | |||||
| chr18:9157585
|
G | A | 188 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-52+20620G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157585 | ||||||
| chr18:9157585
|
G | GTA | 14 | a0002c0002t0001g0070a0002c0002t0001g0080a0002c0002t0001g0152others(11): Show | 14 | HG00323.hp1 HG01168.hp1 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52+20634_-52+2063 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTATA | 3 | a0002c0002t0006g0039a0002c0002t0025g0060a0002c0022t0064g0316 | 3 | HG01167.hp1 HG01255.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-52+20632_-52+2063 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTATATA | 19 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0006g0041others(16): Show | 19 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.-52+20630_-52+2063 others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTATATAT others(3): Show |
3 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0025g0036 | 3 | HG01243.hp1 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-52+20626_-52+2063 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTATATAT others(9): Show |
1 | a0001c0001t0017g0028 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-52+20635_-52+2063 others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTATATAT others(15): Show |
1 | a0004c0004t0004g0288 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-52+20635_-52+2063 others(26): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTGTA | 42 | a0001c0001t0066g0102a0002c0002t0001g0094a0002c0002t0001g0095others(39): Show | 42 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.-52+20621_-52+2062 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTGTGTA | 11 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0035others(8): Show | 11 | HG00735.hp2 HG01243.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.-52+20621_-52+2062 others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTGTGTAT others(3): Show |
1 | a0001c0001t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTGTGTGT others(3): Show |
1 | a0003c0003t0023g0010 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTGTGTGT others(17): Show |
1 | a0001c0024t0074g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(28): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTGTGTGT others(11): Show |
2 | a0001c0001t0034g0030a0001c0001t0034g0031 | 2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-52+20621_-52+2062 others(22): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTGTGTGT others(17): Show |
1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(28): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTGTGTGT others(19): Show |
1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(30): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTGTGTGT others(23): Show |
1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(34): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTGTGTGT others(25): Show |
1 | a0002c0002t0032g0160 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(36): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157585
|
G | GTGTGTGT others(25): Show |
1 | a0002c0002t0032g0161 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(36): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | |||||
| chr18:9157587
|
A | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+20622A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157587 | ||||||
| chr18:9157597
|
A | ATATATAT others(21): Show |
1 | a0004c0004t0004g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-52+20635_-52+2063 others(32): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157597 | |||||
| chr18:9157601
|
G | A | 13 | a0001c0001t0002g0261a0001c0001t0003g0198a0001c0001t0003g0259others(10): Show | 13 | HG00735.hp1 HG01106.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.-52+20636G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157601 | ||||||
| chr18:9157603
|
A | ATATATAT others(20): Show |
1 | a0004c0004t0004g0304 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-52+20639_-52+2064 others(31): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157603 | |||||
| chr18:9157603
|
A | ATATATAT others(12): Show |
1 | a0004c0028t0004g0282 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-52+20639_-52+2064 others(23): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157603 | |||||
| chr18:9157603
|
A | G | 11 | a0001c0001t0002g0261a0001c0001t0003g0198a0001c0001t0003g0259others(8): Show | 11 | HG00735.hp1 HG01106.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.-52+20638A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157603 | ||||||
| chr18:9157603
|
AT | A | 107 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0188others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-52+20655delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157603 | |||||
| chr18:9157604
|
T | TA | 11 | a0001c0001t0002g0261a0001c0001t0003g0198a0001c0001t0003g0259others(8): Show | 11 | HG00735.hp1 HG01106.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.-52+20639_-52+2064 others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157604 | ||||||
| chr18:9157635
|
C | T | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-52+20670C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157635 | ||||||
| chr18:9157955
|
G | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+20990G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157955 | ||||||
| chr18:9158314
|
C | G | 5 | a0001c0001t0016g0177a0005c0006t0007g0176a0005c0006t0007g0178others(2): Show | 5 | HG00099.hp1 HG01255.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+21349C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158314 | ||||||
| chr18:9158328
|
G | A | 1 | a0002c0002t0006g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-52+21363G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158328 | ||||||
| chr18:9158364
|
G | A | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-52+21399G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158364 | ||||||
| chr18:9158512
|
T | C | 1 | a0001c0001t0003g0233 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-52+21547T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158512 | ||||||
| chr18:9158645
|
G | A | 7 | a0003c0003t0001g0077a0003c0003t0001g0081a0003c0003t0001g0082others(4): Show | 7 | NA18943.hp2 NA18957.hp1 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52+21680G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158645 | ||||||
| chr18:9158783
|
G | C | 211 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-52+21818G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158783 | ||||||
| chr18:9158983
|
T | C | 1 | a0002c0002t0009g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-52+22018T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158983 | ||||||
| chr18:9159196
|
A | T | 1 | a0002c0002t0069g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-52+22231A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159196 | ||||||
| chr18:9159225
|
ATATGTG | A | 4 | a0001c0001t0017g0015a0001c0001t0017g0021a0001c0001t0017g0028others(1): Show | 4 | HG02922.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+22264_-52+2226 others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9159225 | |||||
| chr18:9159229
|
G | A | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+22264G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159229 | ||||||
| chr18:9159349
|
A | G | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+22384A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159349 | ||||||
| chr18:9159443
|
A | G | 1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-52+22478A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159443 | ||||||
| chr18:9159492
|
C | T | 1 | a0015c0019t0070g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-52+22527C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159492 | ||||||
| chr18:9159599
|
A | AT | 201 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0188others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-52+22647dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9159599 | |||||
| chr18:9159599
|
A | ATT | 9 | a0002c0002t0006g0038a0002c0002t0043g0040a0004c0004t0018g0299others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-52+22646_-52+2264 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9159599 | |||||
| chr18:9159963
|
C | T | 2 | a0004c0004t0004g0308a0007c0027t0004g0309 | 2 | HG00639.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-51-22419C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159963 | ||||||
| chr18:9159971
|
A | G | 1 | a0003c0003t0001g0106 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-51-22411A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159971 | ||||||
| chr18:9159998
|
G | A | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-22384G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159998 | ||||||
| chr18:9160070
|
G | C | 1 | a0002c0002t0006g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-51-22312G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160070 | ||||||
| chr18:9160191
|
G | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-22191G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160191 | ||||||
| chr18:9160441
|
G | GT | 25 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0006g0037others(22): Show | 25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51-21934dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9160441 | |||||
| chr18:9160491
|
C | G | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-21891C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160491 | ||||||
| chr18:9160577
|
T | C | 1 | a0001c0001t0002g0194 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-51-21805T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160577 | ||||||
| chr18:9160648
|
C | G | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-21734C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160648 | ||||||
| chr18:9160668
|
T | A | 2 | a0003c0003t0062g0072a0003c0003t0063g0071 | 2 | NA19057.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-51-21714T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160668 | ||||||
| chr18:9160709
|
C | T | 2 | a0002c0002t0043g0040a0010c0023t0035g0061 | 2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-51-21673C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160709 | ||||||
| chr18:9160915
|
G | T | 1 | a0001c0001t0022g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-51-21467G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160915 | ||||||
| chr18:9160942
|
T | C | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-21440T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160942 | ||||||
| chr18:9161069
|
G | A | 1 | a0001c0012t0003g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-51-21313G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161069 | ||||||
| chr18:9161106
|
G | T | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-21276G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161106 | ||||||
| chr18:9161180
|
A | G | 1 | a0003c0003t0001g0109 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-51-21202A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161180 | ||||||
| chr18:9161354
|
TTTTTA | T | 3 | a0001c0001t0003g0173a0001c0001t0056g0174a0001c0012t0003g0280 | 3 | HG02559.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-51-21014_-51-2101 others(9): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9161354 | |||||
| chr18:9161534
|
C | T | 2 | a0002c0002t0009g0163a0002c0002t0009g0164 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-51-20848C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161534 | ||||||
| chr18:9161577
|
G | A | 1 | a0002c0002t0006g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-51-20805G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161577 | ||||||
| chr18:9161622
|
C | T | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-20760C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161622 | ||||||
| chr18:9161623
|
G | A | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-20759G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161623 | ||||||
| chr18:9161637
|
A | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-20745A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161637 | ||||||
| chr18:9161655
|
T | C | 316 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-51-20727T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161655 | ||||||
| chr18:9161726
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-20656T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161726 | ||||||
| chr18:9161738
|
A | ATG | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-20630_-51-2062 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9161738 | |||||
| chr18:9161740
|
G | A | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-51-20642G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161740 | ||||||
| chr18:9161750
|
G | GTA | 3 | a0002c0008t0006g0048a0002c0008t0006g0049a0002c0015t0006g0047 | 3 | HG01081.hp2 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-51-20631_-51-2063 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9161750 | |||||
| chr18:9161752
|
G | A | 3 | a0002c0008t0006g0048a0002c0008t0006g0049a0002c0015t0006g0047 | 3 | HG01081.hp2 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-51-20630G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161752 | ||||||
| chr18:9161752
|
G | GTA | 22 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0006g0037others(19): Show | 22 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-51-20619_-51-2061 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9161752 | |||||
| chr18:9161754
|
A | G | 8 | a0004c0004t0004g0283a0004c0004t0004g0284a0004c0004t0004g0285others(5): Show | 8 | HG02015.hp1 HG02132.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.-51-20628A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161754 | ||||||
| chr18:9161873
|
C | T | 214 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0188others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-51-20509C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161873 | ||||||
| chr18:9162016
|
C | T | 1 | a0003c0003t0062g0072 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-51-20366C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162016 | ||||||
| chr18:9162197
|
C | T | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-20185C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162197 | ||||||
| chr18:9162224
|
T | G | 215 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-51-20158T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162224 | ||||||
| chr18:9162422
|
T | C | 2 | a0002c0002t0043g0040a0010c0023t0035g0061 | 2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-51-19960T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162422 | ||||||
| chr18:9162444
|
C | T | 1 | a0009c0014t0001g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-51-19938C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162444 | ||||||
| chr18:9162620
|
C | T | 1 | a0001c0001t0017g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-51-19762C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162620 | ||||||
| chr18:9162710
|
C | T | 1 | a0001c0001t0007g0255 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-51-19672C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162710 | ||||||
| chr18:9162804
|
T | C | 138 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-51-19578T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162804 | ||||||
| chr18:9162808
|
G | GT | 138 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-51-19566dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9162808 | |||||
| chr18:9162818
|
A | G | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-19564A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162818 | ||||||
| chr18:9162914
|
T | C | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-19468T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162914 | ||||||
| chr18:9163142
|
C | G | 26 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(23): Show | 26 | HG00639.hp1 HG01934.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51-19240C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9163142 | ||||||
| chr18:9163148
|
T | C | 3 | a0004c0004t0004g0283a0004c0004t0004g0284a0004c0004t0004g0285 | 3 | HG02015.hp1 HG02135.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-51-19234T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9163148 | ||||||
| chr18:9163261
|
G | A | 2 | a0001c0001t0002g0199a0001c0001t0010g0264 | 2 | NA18953.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-51-19121G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9163261 | ||||||
| chr18:9163387
|
G | T | 138 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-51-18995G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9163387 | ||||||
| chr18:9163477
|
T | C | 138 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-51-18905T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9163477 | ||||||
| chr18:9163511
|
C | T | 4 | a0001c0001t0017g0015a0001c0001t0017g0021a0001c0001t0017g0028others(1): Show | 4 | HG02922.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-18871C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9163511 | ||||||
| chr18:9164011
|
G | A | 212 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-51-18371G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164011 | ||||||
| chr18:9164101
|
G | C | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-18281G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164101 | ||||||
| chr18:9164209
|
T | C | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-18173T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164209 | ||||||
| chr18:9164357
|
C | G | 3 | a0002c0002t0019g0056a0002c0002t0019g0057a0002c0002t0019g0058 | 3 | HG01070.hp2 HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-51-18025C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164357 | ||||||
| chr18:9164599
|
C | T | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-17783C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164599 | ||||||
| chr18:9164756
|
G | A | 1 | a0001c0001t0017g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-51-17626G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164756 | ||||||
| chr18:9164761
|
T | G | 128 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-51-17621T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164761 | ||||||
| chr18:9164890
|
C | T | 1 | a0004c0004t0018g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-51-17492C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164890 | ||||||
| chr18:9165215
|
G | A | 1 | a0003c0003t0023g0012 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-51-17167G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165215 | ||||||
| chr18:9165249
|
A | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-17133A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165249 | ||||||
| chr18:9165382
|
G | A | 215 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-51-17000G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165382 | ||||||
| chr18:9165678
|
G | A | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162others(1): Show | 4 | HG01167.hp1 HG01891.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-16704G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165678 | ||||||
| chr18:9165681
|
T | C | 1 | a0001c0001t0005g0200 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-51-16701T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165681 | ||||||
| chr18:9165720
|
T | A | 51 | a0001c0001t0002g0278a0001c0001t0003g0172a0001c0001t0003g0193others(48): Show | 51 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-51-16662T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165720 | ||||||
| chr18:9165743
|
A | T | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | NA18955.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-51-16639A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165743 | ||||||
| chr18:9165815
|
T | C | 216 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.-51-16567T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165815 | ||||||
| chr18:9165863
|
T | TC | 9 | a0001c0001t0003g0271a0001c0001t0005g0200a0001c0001t0005g0262others(6): Show | 9 | HG02647.hp1 HG02738.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51-16512dupC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9165863 | |||||
| chr18:9165871
|
T | C | 39 | a0001c0001t0002g0201a0001c0001t0002g0202a0004c0004t0004g0283others(36): Show | 39 | HG00140.hp1 HG00639.hp1 HG01928.hp1 others(36): Show |
intron_variant | MODIFIER | c.-51-16511T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165871 | ||||||
| chr18:9165877
|
C | T | 91 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-51-16505C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165877 | ||||||
| chr18:9165878
|
A | C | 7 | a0004c0004t0004g0281a0004c0004t0004g0290a0004c0004t0004g0301others(4): Show | 7 | NA18986.hp1 NA18991.hp2 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-16504A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165878 | ||||||
| chr18:9166065
|
G | A | 2 | a0004c0004t0004g0294a0004c0004t0004g0295 | 2 | NA18984.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-51-16317G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166065 | ||||||
| chr18:9166169
|
C | T | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-16213C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166169 | ||||||
| chr18:9166170
|
G | A | 4 | a0002c0002t0009g0086a0002c0002t0009g0163a0002c0002t0009g0164others(1): Show | 4 | HG02886.hp1 HG02965.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-16212G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166170 | ||||||
| chr18:9166236
|
A | G | 25 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0006g0037others(22): Show | 25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51-16146A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166236 | ||||||
| chr18:9166244
|
G | A | 4 | a0002c0002t0001g0013a0002c0002t0001g0157a0002c0002t0001g0158others(1): Show | 4 | NA18941.hp1 NA18971.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-16138G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166244 | ||||||
| chr18:9166283
|
G | C | 1 | a0003c0003t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-51-16099G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166283 | ||||||
| chr18:9166348
|
G | A | 1 | a0006c0005t0015g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-51-16034G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166348 | ||||||
| chr18:9166353
|
C | T | 1 | a0011c0017t0013g0145 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-51-16029C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166353 | ||||||
| chr18:9166380
|
C | T | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-16002C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166380 | ||||||
| chr18:9166406
|
T | C | 43 | a0003c0003t0001g0103a0003c0003t0001g0104a0003c0003t0008g0105others(40): Show | 43 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.-51-15976T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166406 | ||||||
| chr18:9166415
|
G | A | 1 | a0004c0004t0004g0281 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-51-15967G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166415 | ||||||
| chr18:9166450
|
T | C | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-15932T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166450 | ||||||
| chr18:9166459
|
C | T | 1 | a0001c0001t0003g0254 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-51-15923C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166459 | ||||||
| chr18:9166497
|
T | C | 1 | a0001c0001t0005g0228 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-51-15885T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166497 | ||||||
| chr18:9166934
|
T | C | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-15448T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166934 | ||||||
| chr18:9167045
|
C | T | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-15337C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167045 | ||||||
| chr18:9167070
|
GTC | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-15310_-51-1530 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9167070 | |||||
| chr18:9167074
|
A | G | 140 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-51-15308A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167074 | ||||||
| chr18:9167145
|
C | T | 9 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162others(6): Show | 9 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-15237C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167145 | ||||||
| chr18:9167225
|
TTAAAGTA others(10): Show |
T | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-51-15156_-51-1514 others(21): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167225 | ||||||
| chr18:9167245
|
TCTG | T | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-51-15136_-51-1513 others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167245 | ||||||
| chr18:9167249
|
T | G | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-51-15133T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167249 | ||||||
| chr18:9167349
|
G | A | 1 | a0001c0024t0074g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-51-15033G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167349 | ||||||
| chr18:9167370
|
G | T | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-15012G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167370 | ||||||
| chr18:9167423
|
A | G | 6 | a0001c0001t0058g0253a0006c0005t0015g0006a0006c0005t0015g0007others(3): Show | 6 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51-14959A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167423 | ||||||
| chr18:9167440
|
G | T | 1 | a0002c0002t0001g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-51-14942G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167440 | ||||||
| chr18:9167649
|
C | T | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-14733C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167649 | ||||||
| chr18:9167773
|
G | C | 2 | a0001c0001t0054g0003a0001c0001t0075g0004 | 2 | HG00639.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-51-14609G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167773 | ||||||
| chr18:9167796
|
A | G | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-14586A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167796 | ||||||
| chr18:9167875
|
G | A | 1 | a0002c0002t0006g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-51-14507G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167875 | ||||||
| chr18:9167887
|
G | A | 6 | a0001c0009t0033g0019a0001c0009t0033g0020a0002c0002t0032g0160others(3): Show | 6 | HG01167.hp1 HG01891.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51-14495G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167887 | ||||||
| chr18:9167893
|
T | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-14489T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167893 | ||||||
| chr18:9167921
|
G | A | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-14461G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167921 | ||||||
| chr18:9167927
|
AG | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-14452delG | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9167927 | |||||
| chr18:9168045
|
G | T | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-14337G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168045 | ||||||
| chr18:9168053
|
T | C | 1 | a0006c0005t0015g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-51-14329T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168053 | ||||||
| chr18:9168376
|
G | A | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-14006G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168376 | ||||||
| chr18:9168589
|
G | A | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-13793G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168589 | ||||||
| chr18:9168591
|
C | T | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-13791C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168591 | ||||||
| chr18:9168596
|
T | C | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-13786T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168596 | ||||||
| chr18:9168614
|
T | C | 1 | a0002c0002t0008g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-51-13768T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168614 | ||||||
| chr18:9168626
|
C | T | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-13756C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168626 | ||||||
| chr18:9168662
|
G | A | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-51-13720G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168662 | ||||||
| chr18:9168747
|
C | T | 2 | a0001c0001t0029g0252a0001c0001t0029g0269 | 2 | NA18612.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-51-13635C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168747 | ||||||
| chr18:9168809
|
G | C | 1 | a0001c0001t0058g0253 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-51-13573G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168809 | ||||||
| chr18:9168821
|
A | G | 1 | a0002c0002t0001g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-51-13561A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168821 | ||||||
| chr18:9168949
|
C | T | 25 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0006g0037others(22): Show | 25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51-13433C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168949 | ||||||
| chr18:9168975
|
T | G | 2 | a0002c0002t0001g0150a0002c0002t0001g0151 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-51-13407T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168975 | ||||||
| chr18:9168985
|
G | A | 1 | a0002c0002t0001g0135 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-51-13397G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168985 | ||||||
| chr18:9169020
|
C | T | 214 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-51-13362C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169020 | ||||||
| chr18:9169088
|
T | C | 1 | a0003c0003t0001g0014 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-51-13294T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169088 | ||||||
| chr18:9169217
|
G | A | 7 | a0001c0001t0003g0233a0001c0001t0003g0235a0001c0001t0003g0236others(4): Show | 7 | HG00609.hp2 HG02080.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-13165G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169217 | ||||||
| chr18:9169517
|
C | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-12865C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169517 | ||||||
| chr18:9169588
|
T | C | 3 | a0001c0001t0007g0187a0001c0001t0007g0189a0001c0001t0007g0240 | 3 | HG00733.hp1 HG01109.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-51-12794T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169588 | ||||||
| chr18:9169793
|
G | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-12589G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169793 | ||||||
| chr18:9169824
|
T | G | 1 | a0003c0003t0001g0138 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-51-12558T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169824 | ||||||
| chr18:9170001
|
G | T | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-12381G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170001 | ||||||
| chr18:9170012
|
A | C | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-12370A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170012 | ||||||
| chr18:9170030
|
G | A | 3 | a0001c0001t0003g0173a0001c0001t0056g0174a0001c0012t0003g0280 | 3 | HG02559.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-51-12352G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170030 | ||||||
| chr18:9170089
|
G | A | 72 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(69): Show | 72 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.-51-12293G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170089 | ||||||
| chr18:9170173
|
T | A | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-12209T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170173 | ||||||
| chr18:9170246
|
T | C | 1 | a0001c0001t0010g0203 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-51-12136T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170246 | ||||||
| chr18:9170467
|
G | A | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-11915G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170467 | ||||||
| chr18:9170527
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-11855T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170527 | ||||||
| chr18:9170675
|
A | C | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-51-11707A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170675 | ||||||
| chr18:9170740
|
G | A | 1 | a0001c0001t0005g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-51-11642G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170740 | ||||||
| chr18:9171002
|
A | G | 215 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-51-11380A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171002 | ||||||
| chr18:9171009
|
G | A | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-11373G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171009 | ||||||
| chr18:9171034
|
G | A | 4 | a0004c0004t0014g0311a0004c0004t0014g0313a0004c0004t0014g0314others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-11348G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171034 | ||||||
| chr18:9171109
|
G | A | 1 | a0003c0003t0008g0112 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-51-11273G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171109 | ||||||
| chr18:9171134
|
T | C | 1 | a0001c0001t0011g0241 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-51-11248T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171134 | ||||||
| chr18:9171163
|
G | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-11219G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171163 | ||||||
| chr18:9171179
|
C | T | 50 | a0001c0001t0002g0278a0001c0001t0003g0172a0001c0001t0003g0193others(47): Show | 50 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-51-11203C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171179 | ||||||
| chr18:9171228
|
A | T | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-11154A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171228 | ||||||
| chr18:9171403
|
T | C | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-51-10979T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171403 | ||||||
| chr18:9171536
|
T | C | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-10846T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171536 | ||||||
| chr18:9171589
|
A | G | 3 | a0001c0001t0007g0187a0001c0001t0007g0189a0001c0001t0007g0240 | 3 | HG00733.hp1 HG01109.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-51-10793A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171589 | ||||||
| chr18:9171600
|
C | G | 1 | a0001c0010t0002g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-51-10782C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171600 | ||||||
| chr18:9171758
|
C | T | 1 | a0002c0002t0068g0143 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-51-10624C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171758 | ||||||
| chr18:9171855
|
A | T | 4 | a0001c0001t0005g0186a0001c0001t0005g0225a0001c0001t0010g0226others(1): Show | 4 | NA18957.hp2 NA18981.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-10527A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171855 | ||||||
| chr18:9171884
|
G | T | 19 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0006g0037others(16): Show | 19 | HG00733.hp2 HG01081.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-51-10498G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171884 | ||||||
| chr18:9171929
|
A | G | 3 | a0002c0002t0006g0050a0002c0002t0006g0051a0002c0002t0006g0062 | 3 | HG00733.hp2 HG02004.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-51-10453A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171929 | ||||||
| chr18:9172025
|
C | CA | 147 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.-51-10342dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9172025 | |||||
| chr18:9172025
|
C | CAA | 9 | a0001c0001t0003g0242a0001c0001t0003g0254a0001c0001t0005g0228others(6): Show | 9 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51-10343_-51-1034 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9172025 | |||||
| chr18:9172041
|
C | A | 91 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-51-10341C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172041 | ||||||
| chr18:9172084
|
T | TCAAAAAA others(3): Show |
1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-10298_-51-1029 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172084 | ||||||
| chr18:9172085
|
T | G | 1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-10297T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172085 | ||||||
| chr18:9172088
|
C | T | 1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-10294C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172088 | ||||||
| chr18:9172089
|
A | G | 1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-10293A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172089 | ||||||
| chr18:9172339
|
C | G | 26 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(23): Show | 26 | HG00639.hp1 HG01934.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51-10043C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172339 | ||||||
| chr18:9172587
|
T | C | 1 | a0001c0001t0002g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-51-9795T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172587 | ||||||
| chr18:9172620
|
C | G | 1 | a0002c0002t0006g0055 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-51-9762C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172620 | ||||||
| chr18:9172702
|
T | G | 1 | a0003c0003t0001g0144 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-51-9680T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172702 | ||||||
| chr18:9172757
|
C | T | 2 | a0001c0001t0021g0257a0001c0001t0052g0256 | 2 | NA19009.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-51-9625C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172757 | ||||||
| chr18:9172779
|
A | C | 215 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-51-9603A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172779 | ||||||
| chr18:9172853
|
T | C | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-9529T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172853 | ||||||
| chr18:9172886
|
T | A | 4 | a0002c0002t0001g0013a0002c0002t0001g0157a0002c0002t0001g0158others(1): Show | 4 | NA18941.hp1 NA18971.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-9496T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172886 | ||||||
| chr18:9172892
|
G | T | 1 | a0001c0024t0074g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-51-9490G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172892 | ||||||
| chr18:9172925
|
A | G | 211 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-51-9457A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172925 | ||||||
| chr18:9172930
|
C | CT | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-9451dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9172930 | |||||
| chr18:9172961
|
G | A | 3 | a0001c0001t0007g0187a0001c0001t0007g0189a0001c0001t0007g0240 | 3 | HG00733.hp1 HG01109.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-51-9421G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172961 | ||||||
| chr18:9172993
|
G | A | 2 | a0004c0004t0024g0272a0004c0004t0024g0307 | 2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-51-9389G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172993 | ||||||
| chr18:9172996
|
A | G | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-9386A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172996 | ||||||
| chr18:9173067
|
A | AT | 30 | a0001c0001t0003g0001a0001c0001t0003g0251a0001c0001t0003g0271others(27): Show | 30 | HG00423.hp1 HG00639.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.-51-9295dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9173067 | |||||
| chr18:9173067
|
AT | A | 43 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0005g0032others(40): Show | 43 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.-51-9295delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9173067 | |||||
| chr18:9173106
|
A | G | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-9276A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173106 | ||||||
| chr18:9173162
|
C | T | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-51-9220C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173162 | ||||||
| chr18:9173293
|
C | A | 1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-51-9089C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173293 | ||||||
| chr18:9173449
|
A | G | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-8933A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173449 | ||||||
| chr18:9173538
|
A | G | 34 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(31): Show | 34 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.-51-8844A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173538 | ||||||
| chr18:9173545
|
C | T | 1 | a0001c0001t0016g0277 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-51-8837C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173545 | ||||||
| chr18:9173558
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-51-8824G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173558 | ||||||
| chr18:9173577
|
T | C | 215 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-51-8805T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173577 | ||||||
| chr18:9173616
|
T | TG | 48 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0001g0070others(45): Show | 48 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-51-8756dupG | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9173616 | |||||
| chr18:9173616
|
T | TGG | 21 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(18): Show | 21 | HG00140.hp2 HG00733.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51-8757_-51-8756d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9173616 | |||||
| chr18:9173619
|
G | C | 1 | a0004c0004t0004g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-51-8763G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173619 | ||||||
| chr18:9173619
|
G | T | 2 | a0001c0001t0027g0131a0002c0018t0042g0315 | 2 | HG01106.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-51-8763G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173619 | ||||||
| chr18:9173622
|
G | GT | 143 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.-51-8760_-51-8759i others(3): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173622 | ||||||
| chr18:9173623
|
G | T | 1 | a0001c0001t0066g0102 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-51-8759G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173623 | ||||||
| chr18:9173626
|
G | C | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-8756G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173626 | ||||||
| chr18:9173628
|
A | G | 25 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0006g0037others(22): Show | 25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51-8754A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173628 | ||||||
| chr18:9173790
|
G | C | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-8592G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173790 | ||||||
| chr18:9173828
|
G | A | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-8554G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173828 | ||||||
| chr18:9173836
|
G | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-8546G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173836 | ||||||
| chr18:9173888
|
T | G | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-8494T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173888 | ||||||
| chr18:9173891
|
T | G | 1 | a0002c0002t0006g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-51-8491T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173891 | ||||||
| chr18:9173894
|
G | T | 121 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-51-8488G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173894 | ||||||
| chr18:9173935
|
G | C | 69 | a0001c0001t0003g0044a0001c0001t0003g0045a0002c0002t0006g0037others(66): Show | 69 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.-51-8447G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173935 | ||||||
| chr18:9174033
|
C | CA | 3 | a0003c0003t0001g0103a0003c0003t0001g0104a0003c0003t0008g0105 | 3 | NA18943.hp2 NA18957.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-51-8348dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9174033 | |||||
| chr18:9174046
|
T | C | 34 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(31): Show | 34 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.-51-8336T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174046 | ||||||
| chr18:9174123
|
C | T | 13 | a0001c0001t0005g0186a0001c0001t0005g0200a0001c0001t0005g0219others(10): Show | 13 | HG02135.hp1 HG03017.hp1 HG03704.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51-8259C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174123 | ||||||
| chr18:9174206
|
C | T | 1 | a0002c0002t0001g0158 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-51-8176C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174206 | ||||||
| chr18:9174452
|
C | T | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-7930C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174452 | ||||||
| chr18:9174574
|
A | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-7808A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174574 | ||||||
| chr18:9174582
|
C | T | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-7800C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174582 | ||||||
| chr18:9174652
|
C | T | 1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-51-7730C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174652 | ||||||
| chr18:9174660
|
T | C | 2 | a0001c0001t0030g0243a0001c0001t0058g0253 | 2 | NA18983.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-51-7722T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174660 | ||||||
| chr18:9174713
|
G | T | 5 | a0002c0002t0006g0053a0002c0002t0006g0055a0002c0002t0019g0056others(2): Show | 5 | HG00140.hp2 HG01070.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-7669G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174713 | ||||||
| chr18:9174723
|
T | G | 211 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-51-7659T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174723 | ||||||
| chr18:9174741
|
A | G | 123 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.-51-7641A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174741 | ||||||
| chr18:9174787
|
C | A | 1 | a0001c0001t0057g0244 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-51-7595C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174787 | ||||||
| chr18:9174847
|
C | T | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-7535C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174847 | ||||||
| chr18:9174851
|
TG | T | 141 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-51-7530delG | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174851 | ||||||
| chr18:9174852
|
G | T | 2 | a0002c0002t0043g0040a0010c0023t0035g0061 | 2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-51-7530G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174852 | ||||||
| chr18:9174887
|
G | A | 190 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-51-7495G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174887 | ||||||
| chr18:9174929
|
CATTT | C | 205 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-51-7427_-51-7424d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9174929 | |||||
| chr18:9175023
|
C | T | 1 | a0001c0024t0074g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-51-7359C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175023 | ||||||
| chr18:9175100
|
G | A | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-7282G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175100 | ||||||
| chr18:9175174
|
A | C | 1 | a0001c0001t0002g0064 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-51-7208A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175174 | ||||||
| chr18:9175178
|
A | C | 1 | a0002c0002t0001g0101 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-51-7204A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175178 | ||||||
| chr18:9175261
|
G | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-7121G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175261 | ||||||
| chr18:9175288
|
G | A | 1 | a0002c0002t0006g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-51-7094G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175288 | ||||||
| chr18:9175336
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-51-7046T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175336 | ||||||
| chr18:9175448
|
T | C | 24 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(21): Show | 24 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-51-6934T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175448 | ||||||
| chr18:9175523
|
C | CT | 17 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(14): Show | 17 | HG00733.hp2 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.-51-6831dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | |||||
| chr18:9175523
|
C | CTT | 9 | a0001c0001t0002g0064a0001c0001t0002g0274a0001c0001t0017g0028others(6): Show | 9 | HG01106.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-6832_-51-6831d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | |||||
| chr18:9175523
|
C | CTTT | 39 | a0001c0001t0002g0201a0001c0001t0002g0207a0001c0001t0002g0268others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.-51-6833_-51-6831d others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | |||||
| chr18:9175523
|
C | CTTTT | 45 | a0001c0001t0002g0188a0001c0001t0002g0194a0001c0001t0002g0199others(42): Show | 45 | HG00323.hp2 HG01106.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.-51-6834_-51-6831d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | |||||
| chr18:9175523
|
C | CTTTTT | 45 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0195others(42): Show | 45 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-51-6835_-51-6831d others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | |||||
| chr18:9175523
|
C | CTTTTTT | 20 | a0001c0001t0002g0218a0001c0001t0003g0172a0001c0001t0003g0235others(17): Show | 20 | HG00423.hp2 HG00621.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-51-6836_-51-6831d others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | |||||
| chr18:9175523
|
C | CTTTTTTT | 9 | a0001c0001t0003g0001a0001c0001t0003g0249a0001c0001t0003g0259others(6): Show | 9 | HG00735.hp1 HG01515.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-6837_-51-6831d others(9): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | |||||
| chr18:9175523
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0041g0169a0005c0006t0007g0178a0005c0006t0007g0179 | 3 | HG00099.hp1 HG01255.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-51-6841_-51-6831d others(13): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | |||||
| chr18:9175523
|
CT | C | 84 | a0001c0001t0027g0065a0001c0001t0027g0131a0001c0001t0066g0102others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-51-6831delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | |||||
| chr18:9175541
|
T | TC | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-6841_-51-6840i others(3): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175541 | ||||||
| chr18:9175565
|
T | C | 1 | a0006c0005t0015g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-51-6817T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175565 | ||||||
| chr18:9175568
|
T | C | 215 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-51-6814T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175568 | ||||||
| chr18:9175939
|
C | A | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-6443C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175939 | ||||||
| chr18:9175940
|
C | CA | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-6434dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175940 | |||||
| chr18:9176049
|
A | G | 141 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-51-6333A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9176049 | ||||||
| chr18:9176118
|
C | T | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-6264C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9176118 | ||||||
| chr18:9176232
|
G | T | 3 | a0002c0002t0006g0050a0002c0002t0006g0051a0002c0002t0006g0062 | 3 | HG00733.hp2 HG02004.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-51-6150G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9176232 | ||||||
| chr18:9176274
|
C | G | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-6108C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9176274 | ||||||
| chr18:9176524
|
C | T | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-5858C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9176524 | ||||||
| chr18:9177129
|
GC | G | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-5250delC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9177129 | |||||
| chr18:9177299
|
C | T | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-5083C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177299 | ||||||
| chr18:9177316
|
C | T | 2 | a0002c0002t0001g0110a0003c0003t0001g0066 | 2 | HG01361.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-51-5066C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177316 | ||||||
| chr18:9177343
|
T | C | 1 | a0002c0002t0001g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-51-5039T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177343 | ||||||
| chr18:9177379
|
T | C | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | NA18941.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-51-5003T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177379 | ||||||
| chr18:9177433
|
A | ATT | 211 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-51-4948_-51-4947d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9177433 | |||||
| chr18:9177437
|
A | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-4945A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177437 | ||||||
| chr18:9177571
|
G | C | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-4811G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177571 | ||||||
| chr18:9177870
|
T | C | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-4512T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177870 | ||||||
| chr18:9177896
|
T | C | 59 | a0001c0001t0002g0278a0001c0001t0003g0172a0001c0001t0003g0193others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.-51-4486T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177896 | ||||||
| chr18:9177966
|
AAG | A | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-4413_-51-4412d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9177966 | |||||
| chr18:9177974
|
T | C | 84 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(81): Show | 84 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(81): Show |
intron_variant | MODIFIER | c.-51-4408T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177974 | ||||||
| chr18:9178073
|
CT | C | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-4305delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9178073 | |||||
| chr18:9178075
|
T | C | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-4307T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178075 | ||||||
| chr18:9178188
|
A | G | 1 | a0004c0004t0018g0299 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-51-4194A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178188 | ||||||
| chr18:9178308
|
G | A | 68 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(65): Show | 68 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.-51-4074G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178308 | ||||||
| chr18:9178321
|
T | TTC | 46 | a0001c0001t0066g0102a0002c0002t0001g0137a0003c0003t0001g0014others(43): Show | 46 | HG00323.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-51-4040_-51-4039d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9178321 | |||||
| chr18:9178321
|
T | TTCTCTCT others(3): Show |
9 | a0004c0004t0014g0311a0004c0004t0014g0312a0004c0004t0014g0313others(6): Show | 9 | HG00140.hp1 HG01952.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-4052_-51-4051i others(12): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9178321 | |||||
| chr18:9178321
|
TTC | T | 6 | a0001c0001t0002g0199a0001c0001t0005g0209a0001c0001t0005g0225others(3): Show | 6 | HG02523.hp2 NA18953.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-4040_-51-4039d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9178321 | |||||
| chr18:9178325
|
C | CTCTCTCT others(3): Show |
26 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(23): Show | 26 | HG00639.hp1 HG01934.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51-4048_-51-4047i others(12): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9178325 | |||||
| chr18:9178343
|
C | CTCTCTCT others(7): Show |
5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-4039_-51-4038i others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178343 | ||||||
| chr18:9178343
|
C | CTT | 163 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.-51-4039_-51-4038i others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178343 | ||||||
| chr18:9178343
|
C | T | 41 | a0001c0001t0002g0199a0001c0001t0005g0209a0001c0001t0005g0225others(38): Show | 41 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.-51-4039C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178343 | ||||||
| chr18:9178360
|
T | G | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-4022T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178360 | ||||||
| chr18:9178454
|
G | A | 1 | a0015c0019t0070g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-51-3928G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178454 | ||||||
| chr18:9178485
|
G | A | 1 | a0001c0001t0017g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-51-3897G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178485 | ||||||
| chr18:9178503
|
A | G | 4 | a0001c0001t0003g0001a0001c0001t0041g0169a0001c0001t0055g0001others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-3879A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178503 | ||||||
| chr18:9178624
|
A | G | 1 | a0013c0020t0003g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-51-3758A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178624 | ||||||
| chr18:9179034
|
C | T | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-3348C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179034 | ||||||
| chr18:9179130
|
A | G | 4 | a0002c0002t0006g0039a0002c0002t0006g0050a0002c0002t0006g0051others(1): Show | 4 | HG00733.hp2 HG01255.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-3252A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179130 | ||||||
| chr18:9179151
|
A | G | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-3231A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179151 | ||||||
| chr18:9179244
|
T | C | 1 | a0001c0001t0016g0184 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-51-3138T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179244 | ||||||
| chr18:9179249
|
T | C | 127 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.-51-3133T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179249 | ||||||
| chr18:9179349
|
T | C | 1 | a0002c0002t0001g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-51-3033T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179349 | ||||||
| chr18:9179473
|
A | G | 5 | a0002c0002t0006g0053a0002c0002t0006g0055a0002c0002t0019g0056others(2): Show | 5 | HG00140.hp2 HG01070.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-2909A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179473 | ||||||
| chr18:9179540
|
G | C | 1 | a0001c0001t0066g0102 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-51-2842G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179540 | ||||||
| chr18:9179635
|
C | G | 4 | a0001c0001t0017g0015a0001c0001t0017g0021a0001c0001t0017g0028others(1): Show | 4 | HG02922.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-2747C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179635 | ||||||
| chr18:9179848
|
A | G | 1 | a0006c0005t0015g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-51-2534A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179848 | ||||||
| chr18:9179917
|
G | A | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-2465G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179917 | ||||||
| chr18:9179929
|
C | T | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-2453C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179929 | ||||||
| chr18:9180067
|
A | G | 1 | a0001c0001t0002g0274 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-51-2315A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180067 | ||||||
| chr18:9180078
|
T | C | 1 | a0001c0001t0011g0250 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-51-2304T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180078 | ||||||
| chr18:9180099
|
T | G | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-2283T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180099 | ||||||
| chr18:9180108
|
C | T | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-2274C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180108 | ||||||
| chr18:9180156
|
T | C | 1 | a0003c0003t0001g0091 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-51-2226T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180156 | ||||||
| chr18:9180217
|
C | T | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-2165C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180217 | ||||||
| chr18:9180258
|
T | C | 2 | a0001c0001t0017g0021a0001c0001t0017g0028 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-51-2124T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180258 | ||||||
| chr18:9180446
|
T | C | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-1936T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180446 | ||||||
| chr18:9180462
|
G | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-1920G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180462 | ||||||
| chr18:9180467
|
A | G | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-1915A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180467 | ||||||
| chr18:9181119
|
A | G | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-1263A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181119 | ||||||
| chr18:9181329
|
G | A | 3 | a0004c0004t0004g0287a0004c0004t0004g0294a0004c0004t0004g0295 | 3 | NA18960.hp1 NA18984.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-51-1053G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181329 | ||||||
| chr18:9181548
|
G | T | 77 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(74): Show | 77 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.-51-834G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181548 | ||||||
| chr18:9181713
|
G | C | 1 | a0001c0001t0020g0183 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-51-669G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181713 | ||||||
| chr18:9181716
|
A | G | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-666A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181716 | ||||||
| chr18:9181802
|
A | G | 1 | a0003c0003t0001g0121 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-51-580A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181802 | ||||||
| chr18:9181818
|
A | C | 45 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162others(42): Show | 45 | HG00140.hp1 HG00639.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.-51-564A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181818 | ||||||
| chr18:9181965
|
T | C | 3 | a0001c0001t0017g0029a0001c0001t0034g0030a0001c0001t0034g0031 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-51-417T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181965 | ||||||
| chr18:9181976
|
G | A | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-406G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181976 | ||||||
| chr18:9182178
|
C | T | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-204C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182178 | ||||||
| chr18:9182193
|
T | A | 215 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-51-189T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182193 | ||||||
| chr18:9182318
|
T | G | 1 | a0014c0021t0003g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-51-64T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182318 | ||||||
| chr18:9182330
|
G | A | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-52G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182330 | ||||||
| chr18:9182333
|
A | AACTTCAG others(6): Show |
211 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-51-49_-51-48insAC others(11): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182333 | ||||||
| chr18:9182334
|
C | T | 211 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-51-48C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182334 | ||||||
| chr18:9182364
|
T | C | 5 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162others(2): Show | 5 | HG01106.hp2 HG01167.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51-18T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182364 | ||||||
| chr18:9182647
|
C | T | 3 | a0001c0001t0005g0222a0001c0001t0005g0228a0001c0001t0048g0232 | 3 | HG03017.hp1 HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.87+128C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9182647 | ||||||
| chr18:9182998
|
C | T | 211 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.87+479C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9182998 | ||||||
| chr18:9183047
|
G | A | 1 | a0001c0001t0003g0263 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.87+528G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183047 | ||||||
| chr18:9183110
|
A | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+591A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183110 | ||||||
| chr18:9183262
|
G | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+743G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183262 | ||||||
| chr18:9183561
|
T | G | 1 | a0001c0001t0022g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.87+1042T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183561 | ||||||
| chr18:9183673
|
ACTT | A | 47 | a0001c0001t0002g0278a0001c0001t0003g0172a0001c0001t0003g0193others(44): Show | 47 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.87+1158_87+1160del others(3): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9183673 | |||||
| chr18:9183689
|
G | A | 11 | a0001c0001t0027g0065a0001c0001t0027g0131a0002c0002t0001g0124others(8): Show | 11 | HG00423.hp1 HG01123.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.87+1170G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183689 | ||||||
| chr18:9183744
|
A | G | 64 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.87+1225A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183744 | ||||||
| chr18:9183921
|
G | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+1402G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183921 | ||||||
| chr18:9184135
|
T | C | 3 | a0001c0001t0017g0029a0001c0001t0034g0030a0001c0001t0034g0031 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.87+1616T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184135 | ||||||
| chr18:9184214
|
T | G | 1 | a0004c0004t0014g0312 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.87+1695T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184214 | ||||||
| chr18:9184392
|
A | AT | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.87+1882dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9184392 | |||||
| chr18:9184467
|
A | G | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.87+1948A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184467 | ||||||
| chr18:9184497
|
A | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.87+1978A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184497 | ||||||
| chr18:9184611
|
G | A | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.87+2092G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184611 | ||||||
| chr18:9184672
|
G | A | 1 | a0001c0001t0003g0271 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.87+2153G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184672 | ||||||
| chr18:9184704
|
A | C | 1 | a0001c0007t0028g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.87+2185A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184704 | ||||||
| chr18:9184714
|
C | T | 2 | a0001c0001t0012g0212a0001c0001t0012g0213 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.87+2195C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184714 | ||||||
| chr18:9184861
|
T | C | 1 | a0001c0001t0022g0170 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.87+2342T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184861 | ||||||
| chr18:9184875
|
C | T | 2 | a0001c0001t0005g0017a0001c0001t0005g0262 | 2 | NA19058.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.87+2356C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184875 | ||||||
| chr18:9184902
|
C | T | 1 | a0003c0003t0001g0109 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.87+2383C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184902 | ||||||
| chr18:9185069
|
A | G | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.87+2550A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185069 | ||||||
| chr18:9185131
|
C | G | 212 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.87+2612C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185131 | ||||||
| chr18:9185304
|
A | C | 1 | a0003c0003t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.87+2785A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185304 | ||||||
| chr18:9185313
|
A | G | 1 | a0005c0006t0007g0204 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.87+2794A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185313 | ||||||
| chr18:9185478
|
A | G | 1 | a0001c0001t0030g0243 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.87+2959A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185478 | ||||||
| chr18:9185511
|
T | C | 1 | a0001c0001t0003g0193 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.87+2992T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185511 | ||||||
| chr18:9185740
|
A | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+3221A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185740 | ||||||
| chr18:9185849
|
A | G | 3 | a0001c0007t0028g0025a0002c0002t0043g0040a0010c0023t0035g0061 | 3 | HG02109.hp1 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.87+3330A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185849 | ||||||
| chr18:9185986
|
A | G | 1 | a0004c0004t0037g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.87+3467A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185986 | ||||||
| chr18:9186006
|
G | A | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.87+3487G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186006 | ||||||
| chr18:9186009
|
A | G | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.87+3490A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186009 | ||||||
| chr18:9186079
|
T | C | 1 | a0002c0002t0069g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.87+3560T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186079 | ||||||
| chr18:9186094
|
C | T | 2 | a0001c0001t0002g0199a0001c0001t0010g0264 | 2 | NA18953.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.87+3575C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186094 | ||||||
| chr18:9186137
|
A | AT | 37 | a0001c0001t0010g0203a0001c0001t0017g0029a0001c0001t0020g0183others(34): Show | 37 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.87+3639dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9186137 | |||||
| chr18:9186137
|
AT | A | 14 | a0001c0001t0002g0064a0001c0001t0011g0250a0001c0001t0012g0212others(11): Show | 14 | HG01069.hp1 HG01167.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.87+3639delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9186137 | |||||
| chr18:9186204
|
G | A | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.87+3685G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186204 | ||||||
| chr18:9186237
|
A | G | 1 | a0003c0003t0001g0138 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.87+3718A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186237 | ||||||
| chr18:9186486
|
G | A | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0002c0002t0001g0154 | 3 | HG01099.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.87+3967G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186486 | ||||||
| chr18:9186545
|
T | G | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.87+4026T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186545 | ||||||
| chr18:9186686
|
G | T | 22 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(19): Show | 22 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.87+4167G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186686 | ||||||
| chr18:9186750
|
C | CT | 26 | a0001c0001t0003g0263a0001c0001t0005g0200a0001c0001t0007g0255others(23): Show | 26 | HG00609.hp1 HG00735.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.87+4251dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9186750 | |||||
| chr18:9186750
|
CT | C | 47 | a0001c0001t0005g0225a0001c0001t0012g0212a0002c0002t0001g0127others(44): Show | 47 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.87+4251delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9186750 | |||||
| chr18:9186791
|
C | G | 212 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.87+4272C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186791 | ||||||
| chr18:9186795
|
G | A | 212 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.87+4276G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186795 | ||||||
| chr18:9186799
|
C | T | 35 | a0001c0001t0005g0225a0004c0004t0004g0281a0004c0004t0004g0283others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.87+4280C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186799 | ||||||
| chr18:9186821
|
A | G | 41 | a0001c0001t0005g0225a0004c0004t0004g0281a0004c0004t0004g0283others(38): Show | 41 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.87+4302A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186821 | ||||||
| chr18:9186876
|
C | T | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.87+4357C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186876 | ||||||
| chr18:9186901
|
G | A | 1 | a0002c0002t0006g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.87+4382G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186901 | ||||||
| chr18:9186952
|
C | T | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.87+4433C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186952 | ||||||
| chr18:9186973
|
GAATGGTC others(3): Show |
G | 1 | a0003c0003t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.87+4456_87+4465del others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9186973 | |||||
| chr18:9187056
|
T | C | 1 | a0003c0003t0023g0097 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.87+4537T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187056 | ||||||
| chr18:9187169
|
A | G | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.87+4650A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187169 | ||||||
| chr18:9187506
|
A | G | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.87+4987A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187506 | ||||||
| chr18:9187600
|
A | G | 1 | a0001c0001t0021g0267 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.87+5081A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187600 | ||||||
| chr18:9187612
|
T | C | 1 | a0001c0001t0046g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.87+5093T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187612 | ||||||
| chr18:9187632
|
G | A | 1 | a0004c0004t0004g0286 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.87+5113G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187632 | ||||||
| chr18:9187730
|
G | T | 2 | a0002c0002t0001g0150a0002c0002t0001g0151 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.87+5211G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187730 | ||||||
| chr18:9187741
|
G | C | 1 | a0003c0003t0001g0073 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.87+5222G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187741 | ||||||
| chr18:9187793
|
A | G | 1 | a0003c0003t0001g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.87+5274A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187793 | ||||||
| chr18:9187874
|
C | T | 1 | a0015c0019t0070g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.87+5355C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187874 | ||||||
| chr18:9187875
|
G | A | 2 | a0005c0006t0007g0178a0005c0006t0007g0179 | 2 | HG00099.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.87+5356G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187875 | ||||||
| chr18:9187922
|
T | C | 1 | a0002c0002t0069g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.87+5403T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187922 | ||||||
| chr18:9187991
|
A | G | 8 | a0001c0001t0017g0015a0001c0001t0017g0021a0001c0001t0017g0028others(5): Show | 8 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.87+5472A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187991 | ||||||
| chr18:9188136
|
A | C | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0013t0071g0162 | 3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.87+5617A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188136 | ||||||
| chr18:9188177
|
G | A | 1 | a0001c0001t0003g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.87+5658G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188177 | ||||||
| chr18:9188190
|
C | G | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.87+5671C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188190 | ||||||
| chr18:9188229
|
A | G | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.87+5710A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188229 | ||||||
| chr18:9188365
|
G | C | 4 | a0002c0002t0001g0123a0002c0002t0001g0133a0002c0002t0059g0129others(1): Show | 4 | NA18983.hp1 NA19006.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+5846G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188365 | ||||||
| chr18:9188369
|
G | A | 1 | a0002c0002t0001g0116 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.87+5850G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188369 | ||||||
| chr18:9188425
|
T | A | 6 | a0001c0001t0003g0233a0001c0001t0003g0235a0001c0001t0003g0236others(3): Show | 6 | HG00609.hp2 HG02080.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.87+5906T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188425 | ||||||
| chr18:9188432
|
C | T | 1 | a0001c0001t0030g0276 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.87+5913C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188432 | ||||||
| chr18:9188856
|
T | C | 217 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.87+6337T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188856 | ||||||
| chr18:9188870
|
G | T | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.87+6351G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188870 | ||||||
| chr18:9188929
|
TG | T | 11 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024others(8): Show | 11 | HG02055.hp1 HG02647.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.87+6412delG | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9188929 | |||||
| chr18:9188947
|
G | C | 4 | a0002c0002t0009g0086a0002c0002t0009g0163a0002c0002t0009g0164others(1): Show | 4 | HG02886.hp1 HG02965.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+6428G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188947 | ||||||
| chr18:9189013
|
A | G | 4 | a0001c0001t0022g0002a0001c0001t0022g0005a0001c0001t0054g0003others(1): Show | 4 | HG00639.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+6494A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9189013 | ||||||
| chr18:9189252
|
A | G | 21 | a0002c0002t0006g0039a0002c0002t0006g0041a0002c0002t0006g0042others(18): Show | 21 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.88-6299A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9189252 | ||||||
| chr18:9189308
|
A | G | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.88-6243A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9189308 | ||||||
| chr18:9189486
|
T | C | 1 | a0002c0002t0001g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.88-6065T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9189486 | ||||||
| chr18:9190187
|
G | C | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.88-5364G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190187 | ||||||
| chr18:9190421
|
G | T | 215 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.88-5130G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190421 | ||||||
| chr18:9190470
|
C | A | 8 | a0003c0003t0001g0087a0003c0003t0001g0091a0003c0003t0001g0092others(5): Show | 8 | NA18939.hp2 NA18967.hp2 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.88-5081C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190470 | ||||||
| chr18:9190595
|
A | G | 28 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(25): Show | 28 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.88-4956A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190595 | ||||||
| chr18:9190644
|
A | G | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.88-4907A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190644 | ||||||
| chr18:9190653
|
T | A | 2 | a0002c0002t0001g0127a0002c0002t0008g0126 | 2 | HG03942.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.88-4898T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190653 | ||||||
| chr18:9190927
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.88-4624T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190927 | ||||||
| chr18:9190930
|
G | A | 1 | a0002c0002t0006g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.88-4621G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190930 | ||||||
| chr18:9191023
|
C | T | 213 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.88-4528C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9191023 | ||||||
| chr18:9191422
|
A | G | 126 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.88-4129A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9191422 | ||||||
| chr18:9191493
|
T | G | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.88-4058T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9191493 | ||||||
| chr18:9192130
|
C | T | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.88-3421C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192130 | ||||||
| chr18:9192310
|
A | G | 171 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.88-3241A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192310 | ||||||
| chr18:9192397
|
G | A | 1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.88-3154G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192397 | ||||||
| chr18:9192419
|
G | T | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.88-3132G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192419 | ||||||
| chr18:9192649
|
T | C | 1 | a0015c0019t0070g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.88-2902T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192649 | ||||||
| chr18:9192672
|
C | T | 1 | a0001c0001t0007g0255 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.88-2879C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192672 | ||||||
| chr18:9192705
|
C | G | 11 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0205others(8): Show | 11 | HG02015.hp2 HG02129.hp1 HG03490.hp1 others(8): Show |
intron_variant | MODIFIER | c.88-2846C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192705 | ||||||
| chr18:9192709
|
C | CT | 141 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.88-2833dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9192709 | |||||
| chr18:9192722
|
G | A | 1 | a0001c0001t0016g0177 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.88-2829G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192722 | ||||||
| chr18:9192809
|
G | A | 1 | a0004c0004t0004g0301 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.88-2742G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192809 | ||||||
| chr18:9192812
|
G | A | 5 | a0001c0001t0017g0015a0001c0001t0017g0021a0001c0001t0017g0028others(2): Show | 5 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-2739G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192812 | ||||||
| chr18:9192931
|
G | A | 1 | a0001c0001t0005g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.88-2620G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192931 | ||||||
| chr18:9193094
|
A | G | 1 | a0003c0003t0008g0084 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.88-2457A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193094 | ||||||
| chr18:9193135
|
A | AT | 48 | a0001c0001t0002g0199a0001c0001t0003g0044a0001c0001t0003g0045others(45): Show | 48 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.88-2397dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9193135 | |||||
| chr18:9193135
|
AT | A | 7 | a0001c0001t0002g0064a0001c0009t0033g0019a0001c0009t0033g0020others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.88-2397delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9193135 | |||||
| chr18:9193173
|
T | A | 1 | a0001c0001t0005g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.88-2378T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193173 | ||||||
| chr18:9193265
|
A | G | 6 | a0001c0001t0003g0172a0001c0001t0003g0249a0001c0001t0007g0255others(3): Show | 6 | HG01168.hp2 HG01361.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.88-2286A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193265 | ||||||
| chr18:9193516
|
T | G | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-2035T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193516 | ||||||
| chr18:9193525
|
T | G | 4 | a0001c0001t0003g0001a0001c0001t0041g0169a0001c0001t0055g0001others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.88-2026T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193525 | ||||||
| chr18:9193529
|
G | T | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.88-2022G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193529 | ||||||
| chr18:9193569
|
C | T | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.88-1982C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193569 | ||||||
| chr18:9193640
|
C | T | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.88-1911C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193640 | ||||||
| chr18:9193729
|
A | G | 1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.88-1822A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193729 | ||||||
| chr18:9193909
|
A | G | 1 | a0004c0004t0004g0285 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.88-1642A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193909 | ||||||
| chr18:9194107
|
A | G | 2 | a0004c0004t0004g0283a0004c0004t0004g0284 | 2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.88-1444A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194107 | ||||||
| chr18:9194172
|
G | A | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.88-1379G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194172 | ||||||
| chr18:9194216
|
C | A | 143 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.88-1335C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194216 | ||||||
| chr18:9194327
|
T | TTTTA | 71 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(68): Show | 71 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.88-1181_88-1178dup others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9194327 | |||||
| chr18:9194327
|
T | TTTTATTT others(1): Show |
11 | a0002c0002t0001g0013a0002c0002t0001g0124a0002c0002t0001g0125others(8): Show | 11 | HG00621.hp1 HG02886.hp1 NA18906.hp2 others(8): Show |
intron_variant | MODIFIER | c.88-1185_88-1178dup others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9194327 | |||||
| chr18:9194327
|
TTTTA | T | 40 | a0001c0001t0002g0215a0001c0001t0002g0216a0001c0001t0002g0218others(37): Show | 40 | HG00099.hp1 HG01255.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.88-1181_88-1178del others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9194327 | |||||
| chr18:9194327
|
TTTTATTT others(1): Show |
T | 137 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(134): Show | 137 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.88-1185_88-1178del others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9194327 | |||||
| chr18:9194327
|
TTTTATTT others(13): Show |
T | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.88-1197_88-1178del others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9194327 | |||||
| chr18:9194327
|
TTTTATTT others(17): Show |
T | 6 | a0001c0001t0017g0015a0006c0005t0015g0006a0006c0005t0015g0007others(3): Show | 6 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.88-1201_88-1178del others(24): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9194327 | |||||
| chr18:9194433
|
T | C | 1 | a0001c0001t0029g0269 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.88-1118T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194433 | ||||||
| chr18:9194734
|
C | T | 2 | a0001c0001t0002g0199a0001c0001t0010g0264 | 2 | NA18953.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.88-817C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194734 | ||||||
| chr18:9194749
|
T | C | 6 | a0001c0001t0017g0015a0006c0005t0015g0006a0006c0005t0015g0007others(3): Show | 6 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.88-802T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194749 | ||||||
| chr18:9194778
|
A | G | 2 | a0005c0006t0007g0178a0005c0006t0007g0179 | 2 | HG00099.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.88-773A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194778 | ||||||
| chr18:9194854
|
A | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-697A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194854 | ||||||
| chr18:9195165
|
C | T | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.88-386C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9195165 | ||||||
| chr18:9195183
|
G | C | 66 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(63): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.88-368G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9195183 | ||||||
| chr18:9195368
|
A | G | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-183A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9195368 | ||||||
| chr18:9195534
|
A | G | 2 | a0001c0001t0034g0030a0001c0001t0034g0031 | 2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88-17A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9195534 | ||||||
| chr18:9196108
|
A | AAC | 9 | a0002c0002t0001g0096a0002c0002t0001g0100a0002c0002t0001g0137others(6): Show | 9 | HG01099.hp2 HG02148.hp1 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+452_235+453dup others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196108 | |||||
| chr18:9196108
|
A | AACAC | 10 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(7): Show | 10 | HG01106.hp2 HG01243.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+450_235+453dup others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196108 | |||||
| chr18:9196108
|
AAC | A | 17 | a0002c0002t0001g0124a0002c0002t0001g0125a0002c0002t0001g0127others(14): Show | 17 | HG01361.hp1 HG01433.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.235+452_235+453del others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196108 | |||||
| chr18:9196108
|
AACAC | A | 12 | a0001c0001t0003g0001a0001c0001t0003g0044a0001c0001t0003g0045others(9): Show | 12 | HG02071.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.235+450_235+453del others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196108 | |||||
| chr18:9196108
|
AACACACA others(3): Show |
A | 1 | a0001c0001t0017g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.235+444_235+453del others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196108 | |||||
| chr18:9196108
|
AACACACA others(11): Show |
A | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.235+436_235+453del others(18): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196108 | |||||
| chr18:9196110
|
C | CACACACA others(60): Show |
2 | a0004c0004t0004g0287a0004c0028t0004g0282 | 2 | NA18960.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.235+441_235+442ins others(67): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196110 | |||||
| chr18:9196112
|
C | CACACACA others(58): Show |
4 | a0004c0004t0004g0285a0004c0004t0004g0292a0004c0004t0004g0300others(1): Show | 4 | NA18955.hp2 NA18973.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+441_235+442ins others(65): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196112 | |||||
| chr18:9196114
|
C | CACACACA others(58): Show |
2 | a0004c0004t0004g0286a0004c0004t0014g0312 | 2 | HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.235+443_235+444ins others(65): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196114 | |||||
| chr18:9196114
|
C | CACACACA others(56): Show |
7 | a0004c0004t0004g0288a0004c0004t0004g0296a0004c0004t0004g0297others(4): Show | 7 | HG02132.hp2 HG03209.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+441_235+442ins others(63): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196114 | |||||
| chr18:9196116
|
C | CACACACA others(56): Show |
2 | a0004c0004t0018g0291a0004c0004t0024g0272 | 2 | HG03654.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.235+443_235+444ins others(63): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196116 | |||||
| chr18:9196116
|
C | CACACACA others(54): Show |
18 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(15): Show | 18 | HG00140.hp1 HG00639.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.235+441_235+442ins others(61): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196116 | |||||
| chr18:9196118
|
C | CACACACA others(54): Show |
2 | a0001c0001t0034g0031a0008c0026t0039g0016 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.235+443_235+444ins others(61): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196118 | |||||
| chr18:9196120
|
C | CACACACA others(58): Show |
1 | a0014c0021t0003g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.235+449_235+450ins others(65): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196120 | |||||
| chr18:9196120
|
C | CACACACA others(54): Show |
4 | a0001c0001t0017g0015a0001c0007t0028g0025a0001c0007t0028g0026others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+445_235+446ins others(61): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196120 | |||||
| chr18:9196120
|
C | CACACACA others(52): Show |
8 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024others(5): Show | 8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+443_235+444ins others(59): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196120 | |||||
| chr18:9196120
|
C | CACACACA others(50): Show |
5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+441_235+442ins others(57): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196120 | |||||
| chr18:9196120
|
C | CACACACA others(48): Show |
2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.235+439_235+440ins others(55): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196120 | |||||
| chr18:9196122
|
C | CACACACA others(58): Show |
1 | a0002c0002t0006g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.235+451_235+452ins others(65): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | |||||
| chr18:9196122
|
C | CACACACA others(56): Show |
4 | a0001c0001t0003g0271a0002c0002t0006g0041a0002c0002t0026g0043others(1): Show | 4 | HG02717.hp2 HG02738.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+449_235+450ins others(63): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | |||||
| chr18:9196122
|
C | CACACACA others(54): Show |
19 | a0001c0001t0002g0268a0001c0001t0005g0217a0002c0002t0006g0037others(16): Show | 19 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.235+447_235+448ins others(61): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | |||||
| chr18:9196122
|
C | CACACACA others(52): Show |
4 | a0001c0001t0002g0064a0001c0001t0002g0205a0001c0001t0051g0230others(1): Show | 4 | HG03239.hp1 HG04199.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+445_235+446ins others(59): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | |||||
| chr18:9196122
|
C | CACACACA others(50): Show |
1 | a0001c0001t0002g0188 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.235+443_235+444ins others(57): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | |||||
| chr18:9196122
|
C | CACACACA others(44): Show |
2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.235+437_235+438ins others(51): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | |||||
| chr18:9196122
|
C | CACACACA others(40): Show |
1 | a0002c0002t0025g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.235+434_235+435ins others(47): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | |||||
| chr18:9196124
|
C | CACACACA others(54): Show |
1 | a0001c0012t0003g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.235+449_235+450ins others(61): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196124 | |||||
| chr18:9196124
|
C | CACACACA others(52): Show |
18 | a0001c0001t0003g0246a0001c0001t0003g0275a0001c0001t0011g0241others(15): Show | 18 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.235+447_235+448ins others(59): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196124 | |||||
| chr18:9196124
|
C | CACACACA others(50): Show |
89 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0194others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.235+445_235+446ins others(57): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196124 | |||||
| chr18:9196124
|
C | CACACACA others(42): Show |
1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.235+437_235+438ins others(49): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196124 | |||||
| chr18:9196126
|
C | CACACACA others(50): Show |
1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.235+447_235+448ins others(57): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196126 | |||||
| chr18:9196126
|
C | CACACACA others(48): Show |
1 | a0001c0001t0002g0278 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.235+445_235+446ins others(55): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196126 | |||||
| chr18:9196189
|
T | TAC | 36 | a0001c0001t0003g0275a0001c0001t0005g0032a0001c0001t0005g0033others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.235+524_235+525dup others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACAC | 12 | a0001c0001t0002g0195a0001c0001t0005g0167a0001c0001t0011g0241others(9): Show | 12 | HG00140.hp1 HG00621.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.235+522_235+525dup others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACACAC | 90 | a0001c0001t0002g0068a0001c0001t0002g0188a0001c0001t0002g0199others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.235+520_235+525dup others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACACACA others(1): Show |
29 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0194others(26): Show | 29 | HG00140.hp2 HG00639.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.235+518_235+525dup others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACACACA others(3): Show |
18 | a0001c0001t0003g0198a0001c0001t0003g0271a0001c0001t0017g0021others(15): Show | 18 | HG01081.hp2 HG01255.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.235+516_235+525dup others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACACACA others(5): Show |
8 | a0001c0001t0009g0024a0001c0001t0031g0248a0001c0001t0075g0004others(5): Show | 8 | HG00733.hp2 HG01243.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+514_235+525dup others(12): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACACACA others(7): Show |
6 | a0001c0001t0009g0022a0001c0001t0009g0023a0002c0002t0006g0052others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+512_235+525dup others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACACACA others(9): Show |
1 | a0002c0002t0025g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.235+510_235+525dup others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACACACA others(70): Show |
1 | a0001c0001t0017g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.235+525_235+526ins others(77): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACACACA others(78): Show |
1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.235+522_235+523ins others(85): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACACACA others(64): Show |
4 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0173others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+518_235+519ins others(71): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACACACA others(66): Show |
3 | a0001c0001t0003g0001a0001c0001t0041g0169a0001c0001t0055g0001 | 3 | HG02895.hp1 HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.235+518_235+519ins others(73): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACACACA others(74): Show |
1 | a0002c0002t0006g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.235+518_235+519ins others(81): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACACACA others(66): Show |
1 | a0001c0001t0002g0201 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.235+516_235+517ins others(73): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
T | TACACACA others(72): Show |
1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.235+514_235+515ins others(79): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
TAC | T | 76 | a0001c0001t0066g0102a0002c0002t0001g0013a0002c0002t0001g0094others(73): Show | 76 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.235+524_235+525del others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196189
|
TACACAC | T | 6 | a0001c0001t0003g0172a0001c0001t0003g0249a0001c0001t0007g0255others(3): Show | 6 | HG01168.hp2 HG01361.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+520_235+525del others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | |||||
| chr18:9196193
|
C | CACACACA others(58): Show |
1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.235+522_235+523ins others(65): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196193 | |||||
| chr18:9196222
|
A | T | 4 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0173others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+524A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196222 | ||||||
| chr18:9196326
|
C | T | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.235+628C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196326 | ||||||
| chr18:9196530
|
T | C | 171 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.235+832T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196530 | ||||||
| chr18:9196606
|
T | A | 1 | a0003c0003t0001g0088 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.235+908T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196606 | ||||||
| chr18:9196652
|
T | G | 64 | a0001c0001t0002g0278a0001c0001t0003g0001a0001c0001t0003g0172others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.235+954T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196652 | ||||||
| chr18:9196773
|
C | T | 1 | a0001c0001t0005g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.235+1075C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196773 | ||||||
| chr18:9196786
|
C | T | 1 | a0002c0002t0069g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.235+1088C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196786 | ||||||
| chr18:9196873
|
T | C | 1 | a0001c0001t0005g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.235+1175T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196873 | ||||||
| chr18:9196900
|
G | A | 1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.235+1202G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196900 | ||||||
| chr18:9196957
|
C | T | 2 | a0001c0001t0016g0223a0001c0001t0045g0208 | 2 | HG00099.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.235+1259C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196957 | ||||||
| chr18:9197004
|
C | T | 2 | a0001c0001t0017g0021a0001c0001t0017g0028 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.235+1306C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197004 | ||||||
| chr18:9197069
|
A | T | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.235+1371A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197069 | ||||||
| chr18:9197176
|
T | A | 1 | a0002c0002t0013g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.235+1478T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197176 | ||||||
| chr18:9197214
|
A | G | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.235+1516A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197214 | ||||||
| chr18:9197220
|
G | A | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.235+1522G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197220 | ||||||
| chr18:9197295
|
C | T | 1 | a0002c0002t0006g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.235+1597C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197295 | ||||||
| chr18:9197306
|
T | C | 1 | a0003c0003t0065g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.235+1608T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197306 | ||||||
| chr18:9197374
|
A | G | 63 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(60): Show | 63 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.235+1676A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197374 | ||||||
| chr18:9197460
|
T | C | 1 | a0001c0001t0017g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.235+1762T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197460 | ||||||
| chr18:9197515
|
C | T | 2 | a0001c0001t0003g0193a0001c0001t0012g0192 | 2 | HG01123.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.235+1817C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197515 | ||||||
| chr18:9197528
|
T | G | 218 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.235+1830T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197528 | ||||||
| chr18:9197553
|
TAAAC | T | 58 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(55): Show | 58 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.235+1857_235+1860d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9197553 | |||||
| chr18:9197723
|
T | C | 1 | a0003c0003t0023g0097 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.235+2025T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197723 | ||||||
| chr18:9197817
|
G | T | 2 | a0001c0001t0003g0275a0001c0001t0030g0276 | 2 | HG01081.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.235+2119G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197817 | ||||||
| chr18:9198042
|
T | A | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.235+2344T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198042 | ||||||
| chr18:9198355
|
C | CA | 63 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(60): Show | 63 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.235+2659dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9198355 | |||||
| chr18:9198406
|
C | A | 46 | a0001c0001t0066g0102a0003c0003t0001g0014a0003c0003t0001g0066others(43): Show | 46 | HG00323.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.235+2708C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198406 | ||||||
| chr18:9198544
|
A | G | 4 | a0002c0002t0001g0013a0002c0002t0001g0157a0002c0002t0001g0158others(1): Show | 4 | NA18941.hp1 NA18971.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+2846A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198544 | ||||||
| chr18:9198549
|
AATG | A | 6 | a0002c0002t0006g0053a0002c0002t0006g0054a0002c0002t0006g0055others(3): Show | 6 | HG00140.hp2 HG01070.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+2854_235+2856d others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9198549 | |||||
| chr18:9198625
|
C | T | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.235+2927C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198625 | ||||||
| chr18:9198684
|
G | A | 1 | a0001c0010t0002g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.235+2986G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198684 | ||||||
| chr18:9198697
|
C | T | 1 | a0003c0003t0023g0010 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.235+2999C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198697 | ||||||
| chr18:9198774
|
G | A | 1 | a0001c0001t0034g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.235+3076G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198774 | ||||||
| chr18:9198950
|
G | A | 5 | a0001c0001t0003g0198a0001c0001t0012g0196a0001c0001t0012g0210others(2): Show | 5 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+3252G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198950 | ||||||
| chr18:9199117
|
A | T | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.235+3419A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9199117 | ||||||
| chr18:9199319
|
T | G | 1 | a0001c0001t0002g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.235+3621T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9199319 | ||||||
| chr18:9199388
|
T | C | 5 | a0004c0004t0014g0311a0004c0004t0014g0312a0004c0004t0014g0313others(2): Show | 5 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+3690T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9199388 | ||||||
| chr18:9199419
|
T | C | 1 | a0001c0001t0045g0208 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.235+3721T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9199419 | ||||||
| chr18:9199831
|
G | T | 1 | a0001c0001t0030g0276 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.235+4133G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9199831 | ||||||
| chr18:9200097
|
T | A | 4 | a0004c0004t0014g0311a0004c0004t0014g0313a0004c0004t0014g0314others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-4379T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200097 | ||||||
| chr18:9200103
|
G | A | 1 | a0002c0002t0025g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.236-4373G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200103 | ||||||
| chr18:9200114
|
G | A | 213 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.236-4362G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200114 | ||||||
| chr18:9200296
|
G | C | 1 | a0001c0001t0012g0192 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.236-4180G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200296 | ||||||
| chr18:9200594
|
G | T | 1 | a0001c0001t0012g0192 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.236-3882G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200594 | ||||||
| chr18:9200611
|
C | T | 141 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.236-3865C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200611 | ||||||
| chr18:9200616
|
G | A | 143 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.236-3860G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200616 | ||||||
| chr18:9200812
|
T | C | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.236-3664T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200812 | ||||||
| chr18:9200840
|
G | A | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.236-3636G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200840 | ||||||
| chr18:9201080
|
G | A | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.236-3396G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201080 | ||||||
| chr18:9201369
|
A | G | 3 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0173 | 3 | HG02109.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.236-3107A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201369 | ||||||
| chr18:9201432
|
T | C | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.236-3044T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201432 | ||||||
| chr18:9201641
|
T | C | 1 | a0002c0002t0068g0143 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.236-2835T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201641 | ||||||
| chr18:9201658
|
C | T | 1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.236-2818C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201658 | ||||||
| chr18:9201809
|
GT | G | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.236-2664delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9201809 | |||||
| chr18:9201827
|
CT | C | 46 | a0001c0001t0002g0064a0001c0001t0002g0278a0001c0001t0003g0172others(43): Show | 46 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.236-2636delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9201827 | |||||
| chr18:9201897
|
G | A | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040 | 3 | HG01891.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.236-2579G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201897 | ||||||
| chr18:9201936
|
T | C | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.236-2540T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201936 | ||||||
| chr18:9202101
|
C | G | 5 | a0002c0002t0001g0116a0002c0002t0001g0117a0002c0002t0001g0148others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-2375C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202101 | ||||||
| chr18:9202216
|
A | C | 2 | a0001c0001t0003g0242a0001c0001t0003g0246 | 2 | NA18990.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.236-2260A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202216 | ||||||
| chr18:9202289
|
A | G | 1 | a0001c0001t0058g0253 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.236-2187A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202289 | ||||||
| chr18:9202470
|
A | T | 143 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.236-2006A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202470 | ||||||
| chr18:9202499
|
A | G | 143 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.236-1977A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202499 | ||||||
| chr18:9202571
|
A | T | 1 | a0002c0002t0001g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.236-1905A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202571 | ||||||
| chr18:9202573
|
C | T | 1 | a0003c0003t0001g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.236-1903C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202573 | ||||||
| chr18:9202632
|
C | T | 1 | a0003c0003t0001g0144 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.236-1844C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202632 | ||||||
| chr18:9202657
|
G | A | 1 | a0001c0001t0005g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.236-1819G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202657 | ||||||
| chr18:9202730
|
G | A | 2 | a0001c0001t0017g0021a0001c0001t0017g0028 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.236-1746G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202730 | ||||||
| chr18:9202857
|
A | G | 167 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.236-1619A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202857 | ||||||
| chr18:9202935
|
G | A | 2 | a0001c0001t0017g0021a0001c0001t0017g0028 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.236-1541G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202935 | ||||||
| chr18:9203124
|
T | G | 3 | a0002c0002t0001g0070a0002c0002t0001g0080a0012c0016t0001g0079 | 3 | HG01109.hp1 HG01168.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.236-1352T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203124 | ||||||
| chr18:9203168
|
T | C | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.236-1308T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203168 | ||||||
| chr18:9203218
|
G | A | 1 | a0004c0004t0004g0303 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.236-1258G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203218 | ||||||
| chr18:9203525
|
A | G | 1 | a0004c0004t0018g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.236-951A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203525 | ||||||
| chr18:9203583
|
A | ATG | 25 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(22): Show | 25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.236-881_236-880dup others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9203583 | |||||
| chr18:9203597
|
A | G | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.236-879A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203597 | ||||||
| chr18:9203615
|
A | T | 2 | a0001c0001t0005g0220a0002c0002t0043g0040 | 2 | HG02135.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.236-861A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203615 | ||||||
| chr18:9203654
|
G | T | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-822G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203654 | ||||||
| chr18:9203708
|
G | T | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.236-768G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203708 | ||||||
| chr18:9203718
|
C | A | 6 | a0003c0003t0001g0066a0003c0003t0001g0073a0003c0003t0001g0074others(3): Show | 6 | HG01361.hp1 HG01433.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.236-758C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203718 | ||||||
| chr18:9203730
|
A | G | 1 | a0001c0001t0017g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.236-746A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203730 | ||||||
| chr18:9203890
|
C | T | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.236-586C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203890 | ||||||
| chr18:9203964
|
C | T | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.236-512C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203964 | ||||||
| chr18:9204150
|
C | A | 2 | a0004c0004t0004g0290a0004c0004t0004g0304 | 2 | NA18997.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.236-326C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9204150 | ||||||
| chr18:9204230
|
A | G | 9 | a0002c0002t0001g0124a0002c0002t0001g0125a0002c0002t0001g0127others(6): Show | 9 | HG00423.hp1 HG02071.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.236-246A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9204230 | ||||||
| chr18:9204725
|
T | G | 1 | a0001c0001t0005g0200 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.304+181T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9204725 | ||||||
| chr18:9204738
|
A | C | 2 | a0002c0002t0001g0096a0002c0002t0001g0100 | 2 | HG02148.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.304+194A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9204738 | ||||||
| chr18:9204763
|
C | T | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0002c0002t0001g0154 | 3 | HG01099.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.304+219C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9204763 | ||||||
| chr18:9204890
|
T | G | 1 | a0004c0004t0037g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.304+346T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9204890 | ||||||
| chr18:9204976
|
A | T | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+432A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9204976 | ||||||
| chr18:9205102
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.304+558T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205102 | ||||||
| chr18:9205186
|
T | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+642T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205186 | ||||||
| chr18:9205259
|
G | GT | 316 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.304+720dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr18 | 9205259 | |||||
| chr18:9205322
|
AT | A | 126 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.304+787delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr18 | 9205322 | |||||
| chr18:9205347
|
A | T | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.304+803A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205347 | ||||||
| chr18:9205378
|
T | C | 213 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.304+834T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205378 | ||||||
| chr18:9205665
|
A | G | 1 | a0001c0001t0011g0171 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.304+1121A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205665 | ||||||
| chr18:9205753
|
T | TC | 3 | a0002c0008t0006g0048a0002c0008t0006g0049a0002c0015t0006g0047 | 3 | HG01081.hp2 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.304+1210dupC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr18 | 9205753 | |||||
| chr18:9205779
|
A | G | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.304+1235A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205779 | ||||||
| chr18:9205827
|
T | C | 2 | a0001c0001t0003g0001a0001c0001t0055g0001 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.304+1283T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205827 | ||||||
| chr18:9206687
|
G | A | 5 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0173others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-1970G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9206687 | ||||||
| chr18:9206741
|
A | T | 1 | a0004c0004t0004g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.305-1916A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9206741 | ||||||
| chr18:9206759
|
T | C | 1 | a0001c0001t0003g0254 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.305-1898T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9206759 | ||||||
| chr18:9206931
|
C | T | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.305-1726C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9206931 | ||||||
| chr18:9207168
|
T | C | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.305-1489T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207168 | ||||||
| chr18:9207329
|
A | C | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.305-1328A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207329 | ||||||
| chr18:9207425
|
T | A | 1 | a0002c0002t0001g0100 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.305-1232T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207425 | ||||||
| chr18:9207426
|
G | T | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.305-1231G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207426 | ||||||
| chr18:9207556
|
T | C | 1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.305-1101T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207556 | ||||||
| chr18:9207621
|
T | G | 7 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.305-1036T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207621 | ||||||
| chr18:9207741
|
A | C | 1 | a0001c0001t0034g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.305-916A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207741 | ||||||
| chr18:9208046
|
A | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-611A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9208046 | ||||||
| chr18:9208210
|
T | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-447T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9208210 | ||||||
| chr18:9208235
|
G | A | 1 | a0002c0002t0001g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.305-422G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9208235 | ||||||
| chr18:9208548
|
T | C | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.305-109T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9208548 | ||||||
| chr18:9208821
|
T | C | 1 | a0002c0002t0006g0053 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.451+18T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9208821 | ||||||
| chr18:9208974
|
A | G | 56 | a0001c0001t0002g0278a0001c0001t0003g0172a0001c0001t0003g0193others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.451+171A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9208974 | ||||||
| chr18:9209155
|
T | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+352T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209155 | ||||||
| chr18:9209162
|
A | G | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+359A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209162 | ||||||
| chr18:9209240
|
G | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.451+437G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209240 | ||||||
| chr18:9209456
|
G | A | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.451+653G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209456 | ||||||
| chr18:9209476
|
G | A | 1 | a0004c0004t0024g0307 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.451+673G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209476 | ||||||
| chr18:9209535
|
G | A | 2 | a0002c0002t0009g0163a0002c0002t0009g0164 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.451+732G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209535 | ||||||
| chr18:9209665
|
A | G | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0002c0002t0001g0154 | 3 | HG01099.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.451+862A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209665 | ||||||
| chr18:9209835
|
G | T | 8 | a0004c0004t0004g0283a0004c0004t0004g0284a0004c0004t0004g0285others(5): Show | 8 | HG02015.hp1 HG02132.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.451+1032G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209835 | ||||||
| chr18:9209927
|
T | G | 5 | a0001c0001t0003g0275a0001c0001t0005g0181a0001c0001t0029g0252others(2): Show | 5 | HG01081.hp1 HG02148.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+1124T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209927 | ||||||
| chr18:9210065
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.451+1262T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210065 | ||||||
| chr18:9210095
|
A | G | 1 | a0007c0027t0004g0309 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.451+1292A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210095 | ||||||
| chr18:9210223
|
A | T | 1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.452-1361A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210223 | ||||||
| chr18:9210262
|
C | T | 213 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.452-1322C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210262 | ||||||
| chr18:9210381
|
G | T | 1 | a0003c0003t0001g0085 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.452-1203G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210381 | ||||||
| chr18:9210525
|
A | G | 2 | a0001c0001t0012g0212a0001c0001t0012g0213 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.452-1059A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210525 | ||||||
| chr18:9210539
|
G | T | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-1045G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210539 | ||||||
| chr18:9210550
|
G | A | 2 | a0001c0001t0009g0022a0001c0001t0009g0023 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.452-1034G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210550 | ||||||
| chr18:9210594
|
C | T | 3 | a0002c0002t0019g0056a0002c0002t0019g0057a0002c0002t0019g0058 | 3 | HG01070.hp2 HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.452-990C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210594 | ||||||
| chr18:9210725
|
C | CAAAAAAA others(4): Show |
2 | a0004c0004t0004g0288a0004c0004t0014g0314 | 2 | HG02132.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.452-855_452-845dup others(11): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9210725 | |||||
| chr18:9210725
|
C | CAAAAAAA others(5): Show |
31 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(28): Show | 31 | HG00140.hp1 HG00639.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.452-856_452-845dup others(12): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9210725 | |||||
| chr18:9210725
|
C | CAAAAAAA others(6): Show |
29 | a0001c0001t0005g0017a0001c0001t0017g0028a0002c0002t0006g0037others(26): Show | 29 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.452-857_452-845dup others(13): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9210725 | |||||
| chr18:9210725
|
C | CAAAAAAA others(7): Show |
93 | a0001c0001t0002g0064a0001c0001t0002g0068a0001c0001t0002g0188others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.452-858_452-845dup others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9210725 | |||||
| chr18:9210725
|
C | CAAAAAAA others(8): Show |
53 | a0001c0001t0002g0067a0001c0001t0002g0202a0001c0001t0002g0205others(50): Show | 53 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.452-845_452-844ins others(15): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9210725 | |||||
| chr18:9210725
|
C | CAAAAAAA others(9): Show |
5 | a0001c0001t0005g0220a0001c0001t0010g0226a0001c0001t0010g0227others(2): Show | 5 | HG02135.hp1 HG02809.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-845_452-844ins others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9210725 | |||||
| chr18:9210746
|
A | T | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-838A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210746 | ||||||
| chr18:9210782
|
G | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-802G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210782 | ||||||
| chr18:9211015
|
T | A | 143 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.452-569T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9211015 | ||||||
| chr18:9211088
|
A | G | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.452-496A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9211088 | ||||||
| chr18:9211157
|
A | G | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.452-427A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9211157 | ||||||
| chr18:9211271
|
A | G | 166 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.452-313A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9211271 | ||||||
| chr18:9211368
|
AT | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-208delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9211368 | |||||
| chr18:9211406
|
A | AG | 17 | a0002c0002t0001g0013a0002c0002t0001g0123a0002c0002t0001g0124others(14): Show | 17 | HG00423.hp1 HG02071.hp1 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.452-175dupG | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9211406 | |||||
| chr18:9211928
|
G | A | 1 | a0002c0002t0006g0039 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.652+144G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9211928 | ||||||
| chr18:9211937
|
A | G | 3 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0173 | 3 | HG02109.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.652+153A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9211937 | ||||||
| chr18:9212323
|
T | C | 1 | a0002c0002t0006g0050 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.652+539T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212323 | ||||||
| chr18:9212477
|
A | G | 213 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.652+693A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212477 | ||||||
| chr18:9212478
|
TATATTCT others(2): Show |
T | 213 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.652+695_652+703del others(9): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212478 | ||||||
| chr18:9212537
|
AT | A | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.652+757delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9212537 | |||||
| chr18:9212557
|
G | A | 1 | a0001c0001t0047g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.652+773G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212557 | ||||||
| chr18:9212606
|
T | G | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.652+822T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212606 | ||||||
| chr18:9212641
|
A | G | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.652+857A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212641 | ||||||
| chr18:9212685
|
G | GC | 35 | a0002c0022t0064g0316a0004c0004t0004g0281a0004c0004t0004g0283others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.652+909dupC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9212685 | |||||
| chr18:9212693
|
CAAAATTC others(13): Show |
C | 1 | a0003c0003t0001g0234 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.652+911_652+930del others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9212693 | |||||
| chr18:9212773
|
T | G | 3 | a0001c0001t0020g0182a0001c0001t0020g0183a0001c0001t0020g0197 | 3 | HG01106.hp1 HG01433.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.652+989T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212773 | ||||||
| chr18:9212837
|
C | G | 1 | a0004c0004t0037g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.652+1053C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212837 | ||||||
| chr18:9212928
|
G | T | 1 | a0001c0010t0002g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.652+1144G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212928 | ||||||
| chr18:9213067
|
T | C | 1 | a0002c0002t0001g0132 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.652+1283T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213067 | ||||||
| chr18:9213159
|
A | G | 1 | a0001c0001t0005g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.652+1375A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213159 | ||||||
| chr18:9213276
|
T | C | 2 | a0004c0004t0004g0283a0004c0004t0004g0284 | 2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.652+1492T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213276 | ||||||
| chr18:9213418
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.652+1634G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213418 | ||||||
| chr18:9213751
|
T | C | 1 | a0001c0001t0058g0253 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.652+1967T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213751 | ||||||
| chr18:9213805
|
T | C | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.652+2021T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213805 | ||||||
| chr18:9213934
|
A | G | 1 | a0003c0003t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.652+2150A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213934 | ||||||
| chr18:9214103
|
T | C | 1 | a0001c0001t0017g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.652+2319T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214103 | ||||||
| chr18:9214137
|
C | T | 1 | a0001c0001t0003g0249 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.652+2353C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214137 | ||||||
| chr18:9214138
|
A | G | 213 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.652+2354A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214138 | ||||||
| chr18:9214150
|
T | C | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.652+2366T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214150 | ||||||
| chr18:9214245
|
A | G | 1 | a0001c0001t0022g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.652+2461A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214245 | ||||||
| chr18:9214360
|
TA | T | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.653-2394delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9214360 | |||||
| chr18:9214371
|
G | C | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.653-2387G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214371 | ||||||
| chr18:9214510
|
G | GT | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.653-2247dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9214510 | |||||
| chr18:9214668
|
G | GA | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.653-2084dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9214668 | |||||
| chr18:9214724
|
C | T | 1 | a0001c0001t0003g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.653-2034C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214724 | ||||||
| chr18:9214820
|
G | A | 1 | a0002c0002t0006g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.653-1938G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214820 | ||||||
| chr18:9215054
|
G | A | 1 | a0001c0001t0066g0102 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.653-1704G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9215054 | ||||||
| chr18:9215667
|
A | G | 1 | a0001c0001t0003g0271 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.653-1091A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9215667 | ||||||
| chr18:9215717
|
C | T | 1 | a0003c0003t0008g0084 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.653-1041C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9215717 | ||||||
| chr18:9215743
|
T | TA | 213 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.653-1015_653-1014i others(3): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9215743 | ||||||
| chr18:9215762
|
A | G | 1 | a0001c0001t0003g0254 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.653-996A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9215762 | ||||||
| chr18:9215976
|
T | C | 2 | a0002c0002t0001g0127a0003c0003t0001g0234 | 2 | NA18948.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.653-782T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9215976 | ||||||
| chr18:9216015
|
C | CT | 216 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.653-726dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9216015 | |||||
| chr18:9216116
|
T | C | 1 | a0002c0002t0006g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.653-642T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9216116 | ||||||
| chr18:9216223
|
T | C | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.653-535T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9216223 | ||||||
| chr18:9216601
|
T | C | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.653-157T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9216601 | ||||||
| chr18:9216610
|
T | C | 1 | a0001c0001t0003g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.653-148T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9216610 | ||||||
| chr18:9217208
|
T | C | 1 | a0002c0002t0001g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.795+308T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217208 | ||||||
| chr18:9217236
|
G | A | 316 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.795+336G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217236 | ||||||
| chr18:9217340
|
T | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.795+440T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217340 | ||||||
| chr18:9217413
|
T | C | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+513T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217413 | ||||||
| chr18:9217437
|
A | C | 3 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0173 | 3 | HG02109.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.795+537A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217437 | ||||||
| chr18:9217449
|
A | C | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.795+549A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217449 | ||||||
| chr18:9217473
|
G | A | 211 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.795+573G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217473 | ||||||
| chr18:9217484
|
A | G | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.795+584A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217484 | ||||||
| chr18:9217539
|
A | C | 171 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.795+639A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217539 | ||||||
| chr18:9217551
|
A | G | 1 | a0001c0010t0002g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.795+651A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217551 | ||||||
| chr18:9217743
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.795+843T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217743 | ||||||
| chr18:9217903
|
A | G | 1 | a0001c0001t0031g0248 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.795+1003A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217903 | ||||||
| chr18:9217989
|
C | T | 1 | a0001c0001t0017g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.795+1089C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217989 | ||||||
| chr18:9218017
|
C | T | 3 | a0003c0003t0001g0103a0003c0003t0001g0104a0003c0003t0008g0105 | 3 | NA18943.hp2 NA18957.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+1117C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218017 | ||||||
| chr18:9218116
|
G | A | 1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.795+1216G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218116 | ||||||
| chr18:9218247
|
A | G | 1 | a0002c0002t0001g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.795+1347A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218247 | ||||||
| chr18:9218390
|
G | A | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.795+1490G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218390 | ||||||
| chr18:9218557
|
T | C | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.795+1657T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218557 | ||||||
| chr18:9218568
|
A | G | 213 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.795+1668A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218568 | ||||||
| chr18:9218600
|
T | C | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.795+1700T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218600 | ||||||
| chr18:9218665
|
CT | C | 49 | a0001c0001t0002g0205a0001c0001t0002g0278a0001c0001t0003g0172others(46): Show | 49 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.795+1778delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr18 | 9218665 | |||||
| chr18:9218927
|
T | C | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.795+2027T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218927 | ||||||
| chr18:9218935
|
A | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.795+2035A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218935 | ||||||
| chr18:9219258
|
G | A | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.795+2358G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219258 | ||||||
| chr18:9219319
|
C | T | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.795+2419C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219319 | ||||||
| chr18:9219463
|
G | A | 52 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.796-2389G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219463 | ||||||
| chr18:9219478
|
A | T | 1 | a0001c0001t0034g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.796-2374A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219478 | ||||||
| chr18:9219664
|
G | A | 213 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.796-2188G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219664 | ||||||
| chr18:9219719
|
G | T | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.796-2133G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219719 | ||||||
| chr18:9219758
|
GA | G | 18 | a0001c0001t0046g0190a0002c0002t0006g0037a0002c0002t0006g0038others(15): Show | 18 | HG00733.hp2 HG01081.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.796-2080delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr18 | 9219758 | |||||
| chr18:9219918
|
T | G | 316 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.796-1934T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219918 | ||||||
| chr18:9220464
|
A | G | 1 | a0004c0004t0018g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.796-1388A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9220464 | ||||||
| chr18:9220537
|
G | A | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.796-1315G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9220537 | ||||||
| chr18:9220732
|
G | A | 1 | a0002c0002t0019g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.796-1120G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9220732 | ||||||
| chr18:9220754
|
G | A | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.796-1098G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9220754 | ||||||
| chr18:9220814
|
A | G | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.796-1038A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9220814 | ||||||
| chr18:9221029
|
T | C | 1 | a0001c0001t0003g0279 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.796-823T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221029 | ||||||
| chr18:9221285
|
T | C | 1 | a0001c0001t0020g0183 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.796-567T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221285 | ||||||
| chr18:9221302
|
C | T | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.796-550C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221302 | ||||||
| chr18:9221333
|
G | A | 6 | a0002c0002t0006g0041a0002c0002t0006g0042a0002c0002t0006g0059others(3): Show | 6 | HG02451.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.796-519G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221333 | ||||||
| chr18:9221490
|
G | A | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.796-362G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221490 | ||||||
| chr18:9221605
|
A | T | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.796-247A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221605 | ||||||
| chr18:9221842
|
A | G | 64 | a0001c0001t0066g0102a0002c0002t0001g0013a0002c0002t0001g0123others(61): Show | 64 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.796-10A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221842 | ||||||
| chr18:9222018
|
ACATT | A | 3 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0173 | 3 | HG02109.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.943+23_943+26delTC others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9222018 | |||||
| chr18:9222490
|
A | G | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+491A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9222490 | ||||||
| chr18:9222509
|
A | G | 1 | a0001c0001t0002g0064 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.943+510A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9222509 | ||||||
| chr18:9222657
|
G | A | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.943+658G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9222657 | ||||||
| chr18:9222679
|
C | T | 2 | a0001c0001t0017g0021a0001c0001t0017g0028 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.943+680C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9222679 | ||||||
| chr18:9222877
|
A | T | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.943+878A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9222877 | ||||||
| chr18:9223111
|
T | G | 8 | a0001c0001t0017g0015a0001c0001t0017g0021a0001c0001t0017g0028others(5): Show | 8 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.943+1112T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223111 | ||||||
| chr18:9223259
|
C | CT | 29 | a0001c0001t0017g0015a0001c0001t0017g0021a0001c0001t0017g0028others(26): Show | 29 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.943+1272dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9223259 | |||||
| chr18:9223269
|
T | G | 1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.943+1270T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223269 | ||||||
| chr18:9223314
|
C | T | 3 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0207 | 3 | HG01099.hp1 HG01928.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.943+1315C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223314 | ||||||
| chr18:9223373
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.943+1374C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223373 | ||||||
| chr18:9223376
|
C | A | 1 | a0002c0002t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.943+1377C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223376 | ||||||
| chr18:9223399
|
G | A | 2 | a0005c0006t0007g0176a0005c0006t0007g0270 | 2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.943+1400G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223399 | ||||||
| chr18:9223437
|
C | T | 2 | a0001c0001t0003g0001a0001c0001t0055g0001 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.943+1438C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223437 | ||||||
| chr18:9223923
|
A | C | 1 | a0003c0003t0008g0084 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.943+1924A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223923 | ||||||
| chr18:9223992
|
A | T | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+1993A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223992 | ||||||
| chr18:9224074
|
A | G | 8 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024others(5): Show | 8 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.943+2075A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224074 | ||||||
| chr18:9224093
|
A | T | 1 | a0003c0003t0065g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.943+2094A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224093 | ||||||
| chr18:9224153
|
A | T | 2 | a0001c0001t0021g0257a0001c0001t0052g0256 | 2 | NA19009.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.943+2154A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224153 | ||||||
| chr18:9224267
|
A | G | 1 | a0001c0001t0066g0102 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.943+2268A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224267 | ||||||
| chr18:9224405
|
C | T | 4 | a0001c0001t0021g0191a0001c0001t0021g0257a0001c0001t0021g0267others(1): Show | 4 | HG02132.hp1 NA18969.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+2406C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224405 | ||||||
| chr18:9224441
|
T | C | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.943+2442T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224441 | ||||||
| chr18:9224596
|
C | G | 1 | a0001c0001t0031g0317 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.943+2597C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224596 | ||||||
| chr18:9224638
|
A | G | 3 | a0002c0002t0001g0150a0002c0002t0001g0151a0002c0002t0008g0149 | 3 | HG02258.hp2 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.943+2639A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224638 | ||||||
| chr18:9224746
|
T | C | 3 | a0001c0009t0033g0019a0001c0009t0033g0020a0002c0018t0042g0315 | 3 | HG01106.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.943+2747T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224746 | ||||||
| chr18:9224826
|
T | C | 3 | a0004c0004t0004g0283a0004c0004t0004g0284a0004c0004t0004g0285 | 3 | HG02015.hp1 HG02135.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.943+2827T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224826 | ||||||
| chr18:9224827
|
G | A | 26 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(23): Show | 26 | HG00639.hp1 HG01934.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.943+2828G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224827 | ||||||
| chr18:9225120
|
AAGGCTTG others(328): Show |
A | 145 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.943+3124_943+3458d others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9225120 | |||||
| chr18:9225325
|
T | G | 1 | a0003c0003t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.943+3326T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9225325 | ||||||
| chr18:9225472
|
T | TA | 197 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.943+3490dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9225472 | |||||
| chr18:9225472
|
T | TAA | 7 | a0001c0001t0003g0249a0001c0001t0007g0255a0001c0007t0028g0025others(4): Show | 7 | HG02109.hp1 HG02273.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.943+3489_943+3490d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9225472 | |||||
| chr18:9225472
|
TA | T | 6 | a0001c0001t0066g0102a0002c0002t0001g0095a0002c0002t0001g0154others(3): Show | 6 | HG01070.hp1 HG01099.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.943+3490delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9225472 | |||||
| chr18:9225612
|
G | A | 1 | a0003c0003t0001g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.943+3613G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9225612 | ||||||
| chr18:9225955
|
T | TGG | 63 | a0001c0001t0066g0102a0002c0002t0001g0013a0002c0002t0001g0123others(60): Show | 63 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.943+3957_943+3958i others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9225955 | |||||
| chr18:9226057
|
A | G | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.943+4058A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226057 | ||||||
| chr18:9226063
|
T | C | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.943+4064T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226063 | ||||||
| chr18:9226161
|
C | T | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.943+4162C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226161 | ||||||
| chr18:9226191
|
A | G | 1 | a0002c0002t0013g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.943+4192A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226191 | ||||||
| chr18:9226229
|
G | A | 2 | a0002c0002t0001g0132a0002c0002t0008g0134 | 2 | HG00423.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.943+4230G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226229 | ||||||
| chr18:9226235
|
G | A | 2 | a0001c0001t0003g0001a0001c0001t0055g0001 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.943+4236G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226235 | ||||||
| chr18:9226427
|
A | G | 5 | a0001c0001t0017g0015a0001c0001t0017g0021a0001c0001t0017g0028others(2): Show | 5 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+4428A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226427 | ||||||
| chr18:9226433
|
G | GA | 171 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.943+4443dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9226433 | |||||
| chr18:9226510
|
T | C | 151 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.943+4511T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226510 | ||||||
| chr18:9226678
|
G | A | 1 | a0004c0004t0018g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.943+4679G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226678 | ||||||
| chr18:9226697
|
T | TC | 58 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(55): Show | 58 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.943+4700dupC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9226697 | |||||
| chr18:9226699
|
C | T | 1 | a0001c0001t0021g0191 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.943+4700C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226699 | ||||||
| chr18:9226726
|
T | C | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.943+4727T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226726 | ||||||
| chr18:9226731
|
A | G | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.943+4732A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226731 | ||||||
| chr18:9226743
|
A | T | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.943+4744A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226743 | ||||||
| chr18:9226921
|
G | A | 1 | a0001c0001t0011g0250 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.943+4922G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226921 | ||||||
| chr18:9226997
|
C | T | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.943+4998C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226997 | ||||||
| chr18:9227015
|
C | T | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+5016C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227015 | ||||||
| chr18:9227160
|
A | G | 1 | a0015c0019t0070g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.943+5161A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227160 | ||||||
| chr18:9227525
|
G | A | 1 | a0001c0001t0027g0131 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.943+5526G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227525 | ||||||
| chr18:9227545
|
G | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+5546G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227545 | ||||||
| chr18:9227664
|
G | T | 1 | a0001c0001t0034g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.943+5665G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227664 | ||||||
| chr18:9227937
|
G | T | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.943+5938G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227937 | ||||||
| chr18:9227962
|
C | G | 1 | a0002c0002t0006g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.943+5963C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227962 | ||||||
| chr18:9227997
|
C | T | 4 | a0004c0004t0004g0292a0004c0004t0004g0300a0004c0004t0036g0293others(1): Show | 4 | NA18967.hp1 NA18973.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+5998C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227997 | ||||||
| chr18:9228005
|
A | C | 1 | a0013c0020t0003g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.943+6006A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228005 | ||||||
| chr18:9228073
|
G | GGA | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+6074_943+6075i others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228073 | ||||||
| chr18:9228075
|
C | T | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+6076C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228075 | ||||||
| chr18:9228277
|
A | G | 1 | a0001c0001t0034g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.943+6278A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228277 | ||||||
| chr18:9228308
|
G | C | 1 | a0001c0001t0003g0271 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.943+6309G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228308 | ||||||
| chr18:9228454
|
C | G | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.943+6455C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228454 | ||||||
| chr18:9228576
|
C | T | 150 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.943+6577C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228576 | ||||||
| chr18:9228911
|
CT | C | 200 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.943+6924delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9228911 | |||||
| chr18:9229111
|
A | G | 217 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.943+7112A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229111 | ||||||
| chr18:9229170
|
G | C | 1 | a0001c0001t0048g0232 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.943+7171G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229170 | ||||||
| chr18:9229200
|
C | T | 1 | a0002c0002t0006g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.943+7201C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229200 | ||||||
| chr18:9229225
|
G | A | 2 | a0001c0001t0010g0224a0001c0001t0050g0221 | 2 | NA19006.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.943+7226G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229225 | ||||||
| chr18:9229382
|
G | A | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.943+7383G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229382 | ||||||
| chr18:9229484
|
A | G | 1 | a0001c0010t0002g0185 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.943+7485A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229484 | ||||||
| chr18:9229533
|
T | C | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.943+7534T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229533 | ||||||
| chr18:9229878
|
T | C | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.943+7879T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229878 | ||||||
| chr18:9230161
|
T | A | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.943+8162T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230161 | ||||||
| chr18:9230200
|
G | A | 47 | a0001c0001t0002g0278a0001c0001t0003g0172a0001c0001t0003g0193others(44): Show | 47 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.943+8201G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230200 | ||||||
| chr18:9230206
|
T | G | 1 | a0001c0001t0011g0237 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.943+8207T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230206 | ||||||
| chr18:9230280
|
A | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.943+8281A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230280 | ||||||
| chr18:9230355
|
A | G | 1 | a0001c0001t0046g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.943+8356A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230355 | ||||||
| chr18:9230518
|
T | C | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+8519T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230518 | ||||||
| chr18:9230645
|
C | T | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.943+8646C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230645 | ||||||
| chr18:9230655
|
CT | C | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.943+8670delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9230655 | |||||
| chr18:9230658
|
T | C | 130 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.943+8659T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230658 | ||||||
| chr18:9230721
|
C | T | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.943+8722C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230721 | ||||||
| chr18:9230783
|
C | T | 6 | a0004c0004t0004g0290a0004c0004t0004g0301a0004c0004t0004g0302others(3): Show | 6 | NA18991.hp2 NA18992.hp1 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.943+8784C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230783 | ||||||
| chr18:9230835
|
T | A | 127 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0188others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.943+8836T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230835 | ||||||
| chr18:9230836
|
T | A | 1 | a0001c0001t0002g0064 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.943+8837T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230836 | ||||||
| chr18:9230852
|
G | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+8853G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230852 | ||||||
| chr18:9230870
|
G | T | 3 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0207 | 3 | HG01099.hp1 HG01928.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.943+8871G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230870 | ||||||
| chr18:9230937
|
G | A | 1 | a0002c0002t0006g0039 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.943+8938G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230937 | ||||||
| chr18:9231252
|
T | C | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+9253T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231252 | ||||||
| chr18:9231330
|
G | A | 3 | a0001c0001t0017g0021a0001c0001t0017g0028a0015c0019t0070g0266 | 3 | HG02965.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.943+9331G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231330 | ||||||
| chr18:9231368
|
A | G | 5 | a0001c0001t0017g0015a0001c0001t0017g0021a0001c0001t0017g0028others(2): Show | 5 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+9369A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231368 | ||||||
| chr18:9231374
|
G | A | 3 | a0002c0002t0001g0117a0002c0002t0001g0148a0002c0002t0009g0147 | 3 | HG01891.hp1 HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.943+9375G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231374 | ||||||
| chr18:9231417
|
A | G | 145 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.943+9418A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231417 | ||||||
| chr18:9231579
|
G | A | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.943+9580G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231579 | ||||||
| chr18:9231756
|
C | T | 1 | a0001c0001t0010g0226 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.943+9757C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231756 | ||||||
| chr18:9231824
|
C | CA | 181 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.943+9844dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9231824 | |||||
| chr18:9231824
|
C | CAA | 21 | a0001c0001t0003g0279a0001c0001t0005g0219a0002c0002t0001g0125others(18): Show | 21 | HG00733.hp2 HG01081.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.943+9843_943+9844d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9231824 | |||||
| chr18:9231824
|
C | CAAA | 6 | a0002c0002t0001g0124a0002c0002t0006g0053a0002c0002t0006g0055others(3): Show | 6 | HG00140.hp2 HG01070.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.943+9842_943+9844d others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9231824 | |||||
| chr18:9231914
|
T | TTTTCCAT others(4): Show |
68 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(65): Show | 68 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.943+9917_943+9918i others(13): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9231914 | |||||
| chr18:9232009
|
G | T | 1 | a0002c0025t0001g0120 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.943+10010G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232009 | ||||||
| chr18:9232113
|
C | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+10114C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232113 | ||||||
| chr18:9232560
|
G | C | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.943+10561G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232560 | ||||||
| chr18:9232564
|
T | C | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.943+10565T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232564 | ||||||
| chr18:9232676
|
A | G | 1 | a0002c0008t0006g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.943+10677A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232676 | ||||||
| chr18:9232849
|
T | TTTG | 216 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.943+10865_943+1086 others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9232849 | |||||
| chr18:9232868
|
A | G | 217 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.943+10869A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232868 | ||||||
| chr18:9232918
|
C | T | 8 | a0002c0002t0001g0116a0002c0002t0001g0117a0002c0002t0001g0119others(5): Show | 8 | HG01106.hp2 HG01167.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.943+10919C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232918 | ||||||
| chr18:9232932
|
C | T | 1 | a0001c0001t0003g0236 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.943+10933C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232932 | ||||||
| chr18:9233007
|
G | A | 1 | a0001c0001t0031g0248 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.943+11008G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9233007 | ||||||
| chr18:9233009
|
C | G | 1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.943+11010C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9233009 | ||||||
| chr18:9233166
|
A | G | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+11167A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9233166 | ||||||
| chr18:9233602
|
TGTTA | T | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+11607_943+1161 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9233602 | |||||
| chr18:9233638
|
G | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.943+11639G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9233638 | ||||||
| chr18:9233643
|
C | T | 4 | a0001c0001t0005g0200a0001c0001t0005g0219a0001c0001t0010g0224others(1): Show | 4 | NA18991.hp1 NA18992.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+11644C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9233643 | ||||||
| chr18:9233912
|
A | T | 1 | a0001c0001t0046g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.943+11913A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9233912 | ||||||
| chr18:9234049
|
G | A | 2 | a0002c0002t0001g0124a0002c0002t0001g0125 | 2 | NA18963.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.943+12050G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234049 | ||||||
| chr18:9234070
|
C | CA | 147 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.943+12072dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9234070 | |||||
| chr18:9234108
|
G | A | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.943+12109G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234108 | ||||||
| chr18:9234177
|
G | A | 1 | a0001c0001t0002g0195 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.943+12178G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234177 | ||||||
| chr18:9234398
|
G | A | 4 | a0001c0001t0005g0186a0001c0001t0005g0225a0001c0001t0010g0226others(1): Show | 4 | NA18957.hp2 NA18981.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.943+12399G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234398 | ||||||
| chr18:9234480
|
T | G | 1 | a0003c0003t0001g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.943+12481T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234480 | ||||||
| chr18:9234591
|
G | A | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0002c0002t0001g0154 | 3 | HG01099.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.943+12592G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234591 | ||||||
| chr18:9234592
|
G | A | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.943+12593G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234592 | ||||||
| chr18:9234681
|
G | A | 1 | a0001c0001t0048g0232 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.943+12682G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234681 | ||||||
| chr18:9234730
|
C | T | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+12731C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234730 | ||||||
| chr18:9234753
|
G | A | 3 | a0001c0001t0017g0029a0001c0001t0034g0030a0001c0001t0034g0031 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.943+12754G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234753 | ||||||
| chr18:9234776
|
A | G | 148 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.943+12777A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234776 | ||||||
| chr18:9234858
|
T | C | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.943+12859T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234858 | ||||||
| chr18:9234921
|
A | G | 145 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.943+12922A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234921 | ||||||
| chr18:9235075
|
A | G | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.943+13076A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9235075 | ||||||
| chr18:9235084
|
C | T | 2 | a0004c0004t0018g0306a0004c0004t0037g0289 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.943+13085C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9235084 | ||||||
| chr18:9235114
|
CTA | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.943+13118_943+1311 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9235114 | |||||
| chr18:9235274
|
G | A | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.943+13275G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9235274 | ||||||
| chr18:9235482
|
A | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+13483A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9235482 | ||||||
| chr18:9235676
|
G | A | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+13677G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9235676 | ||||||
| chr18:9235950
|
CT | C | 9 | a0001c0001t0005g0225a0001c0001t0007g0189a0001c0001t0056g0174others(6): Show | 9 | HG01884.hp1 HG01943.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.943+13965delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9235950 | |||||
| chr18:9235953
|
T | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+13954T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9235953 | ||||||
| chr18:9236077
|
A | G | 1 | a0004c0004t0004g0284 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.943+14078A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236077 | ||||||
| chr18:9236097
|
A | G | 1 | a0002c0002t0001g0127 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.943+14098A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236097 | ||||||
| chr18:9236227
|
A | G | 1 | a0001c0001t0003g0249 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.943+14228A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236227 | ||||||
| chr18:9236416
|
CA | C | 217 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.943+14423delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9236416 | |||||
| chr18:9236527
|
C | T | 8 | a0003c0003t0001g0066a0003c0003t0001g0073a0003c0003t0001g0074others(5): Show | 8 | HG01361.hp1 HG01433.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.943+14528C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236527 | ||||||
| chr18:9236587
|
A | AT | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.943+14590dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9236587 | |||||
| chr18:9236629
|
A | G | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.943+14630A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236629 | ||||||
| chr18:9236657
|
C | CAT | 216 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.943+14658_943+1465 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236657 | ||||||
| chr18:9236749
|
G | A | 3 | a0002c0002t0019g0056a0002c0002t0019g0057a0002c0002t0019g0058 | 3 | HG01070.hp2 HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.943+14750G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236749 | ||||||
| chr18:9236821
|
C | T | 1 | a0002c0002t0008g0149 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.943+14822C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236821 | ||||||
| chr18:9237258
|
A | G | 4 | a0001c0001t0005g0186a0001c0001t0005g0225a0001c0001t0010g0226others(1): Show | 4 | NA18957.hp2 NA18981.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.943+15259A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9237258 | ||||||
| chr18:9237277
|
T | G | 217 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.943+15278T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9237277 | ||||||
| chr18:9237481
|
G | T | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.943+15482G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9237481 | ||||||
| chr18:9237575
|
G | T | 2 | a0002c0013t0071g0162a0002c0022t0064g0316 | 2 | HG01167.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.943+15576G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9237575 | ||||||
| chr18:9237811
|
G | T | 1 | a0001c0001t0002g0188 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.943+15812G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9237811 | ||||||
| chr18:9237918
|
C | T | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.943+15919C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9237918 | ||||||
| chr18:9238011
|
A | T | 21 | a0001c0001t0003g0198a0001c0001t0003g0242a0001c0001t0003g0246others(18): Show | 21 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(18): Show |
intron_variant | MODIFIER | c.943+16012A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238011 | ||||||
| chr18:9238062
|
C | G | 1 | a0001c0001t0045g0208 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.943+16063C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238062 | ||||||
| chr18:9238207
|
C | T | 2 | a0002c0018t0042g0315a0003c0003t0001g0014 | 2 | HG01106.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.944-16004C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238207 | ||||||
| chr18:9238228
|
C | G | 5 | a0005c0006t0007g0176a0005c0006t0007g0178a0005c0006t0007g0179others(2): Show | 5 | HG00099.hp1 HG01255.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-15983C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238228 | ||||||
| chr18:9238486
|
C | T | 2 | a0003c0003t0001g0144a0008c0026t0039g0016 | 2 | HG03471.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.944-15725C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238486 | ||||||
| chr18:9238487
|
G | A | 5 | a0002c0002t0001g0124a0002c0002t0001g0125a0002c0002t0001g0128others(2): Show | 5 | HG02129.hp2 NA18963.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-15724G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238487 | ||||||
| chr18:9238606
|
G | T | 2 | a0001c0001t0007g0189a0001c0001t0007g0240 | 2 | HG00733.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.944-15605G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238606 | ||||||
| chr18:9238876
|
C | G | 9 | a0001c0001t0003g0198a0001c0001t0012g0196a0001c0001t0012g0210others(6): Show | 9 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.944-15335C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238876 | ||||||
| chr18:9239015
|
G | A | 1 | a0001c0001t0005g0228 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.944-15196G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9239015 | ||||||
| chr18:9239284
|
G | A | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.944-14927G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9239284 | ||||||
| chr18:9239823
|
A | G | 4 | a0002c0002t0001g0127a0002c0002t0001g0132a0002c0002t0008g0126others(1): Show | 4 | HG00423.hp1 HG02071.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.944-14388A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9239823 | ||||||
| chr18:9239841
|
T | G | 5 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-14370T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9239841 | ||||||
| chr18:9240091
|
C | A | 5 | a0004c0004t0014g0311a0004c0004t0014g0312a0004c0004t0014g0313others(2): Show | 5 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-14120C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240091 | ||||||
| chr18:9240102
|
A | G | 3 | a0001c0001t0020g0182a0001c0001t0020g0183a0001c0001t0020g0197 | 3 | HG01106.hp1 HG01433.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.944-14109A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240102 | ||||||
| chr18:9240147
|
G | A | 4 | a0001c0001t0022g0002a0001c0001t0022g0005a0001c0001t0054g0003others(1): Show | 4 | HG00639.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.944-14064G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240147 | ||||||
| chr18:9240208
|
T | G | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-14003T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240208 | ||||||
| chr18:9240415
|
C | T | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-13796C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240415 | ||||||
| chr18:9240635
|
C | G | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-13576C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240635 | ||||||
| chr18:9240720
|
C | G | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-13491C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240720 | ||||||
| chr18:9240796
|
G | C | 2 | a0001c0001t0003g0193a0001c0001t0012g0192 | 2 | HG01123.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.944-13415G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240796 | ||||||
| chr18:9240832
|
T | C | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-13379T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240832 | ||||||
| chr18:9240901
|
T | C | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.944-13310T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240901 | ||||||
| chr18:9241122
|
G | A | 1 | a0001c0007t0028g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.944-13089G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241122 | ||||||
| chr18:9241317
|
C | G | 1 | a0001c0001t0016g0177 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.944-12894C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241317 | ||||||
| chr18:9241373
|
C | T | 3 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0173 | 3 | HG02109.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.944-12838C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241373 | ||||||
| chr18:9241388
|
C | T | 130 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.944-12823C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241388 | ||||||
| chr18:9241463
|
T | C | 2 | a0004c0004t0004g0283a0004c0004t0004g0284 | 2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.944-12748T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241463 | ||||||
| chr18:9241524
|
G | A | 2 | a0002c0013t0071g0162a0002c0022t0064g0316 | 2 | HG01167.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.944-12687G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241524 | ||||||
| chr18:9241526
|
A | C | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.944-12685A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241526 | ||||||
| chr18:9241672
|
A | C | 1 | a0001c0001t0005g0017 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.944-12539A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241672 | ||||||
| chr18:9241783
|
A | G | 1 | a0002c0002t0001g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.944-12428A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241783 | ||||||
| chr18:9241891
|
G | GT | 51 | a0001c0001t0005g0181a0001c0001t0005g0200a0001c0001t0005g0219others(48): Show | 51 | HG00140.hp1 HG00639.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.944-12306dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9241891 | |||||
| chr18:9241891
|
GT | G | 8 | a0001c0001t0003g0242a0001c0001t0003g0246a0003c0003t0001g0085others(5): Show | 8 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.944-12306delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9241891 | |||||
| chr18:9241958
|
C | T | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.944-12253C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241958 | ||||||
| chr18:9241965
|
C | A | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-12246C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241965 | ||||||
| chr18:9241989
|
A | G | 2 | a0003c0003t0001g0138a0003c0003t0001g0139 | 2 | HG00609.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.944-12222A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241989 | ||||||
| chr18:9242056
|
C | A | 1 | a0001c0001t0005g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.944-12155C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9242056 | ||||||
| chr18:9242335
|
G | A | 1 | a0004c0004t0018g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.944-11876G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9242335 | ||||||
| chr18:9242463
|
C | CA | 138 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.944-11739dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9242463 | |||||
| chr18:9242463
|
C | CAA | 10 | a0001c0001t0003g0198a0001c0001t0003g0271a0001c0001t0012g0196others(7): Show | 10 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.944-11740_944-1173 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9242463 | |||||
| chr18:9242495
|
A | T | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-11716A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9242495 | ||||||
| chr18:9242504
|
G | T | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.944-11707G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9242504 | ||||||
| chr18:9242540
|
A | T | 1 | a0001c0001t0005g0225 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.944-11671A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9242540 | ||||||
| chr18:9242577
|
G | A | 1 | a0002c0002t0006g0039 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.944-11634G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9242577 | ||||||
| chr18:9243138
|
A | G | 1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.944-11073A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9243138 | ||||||
| chr18:9243556
|
C | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.944-10655C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9243556 | ||||||
| chr18:9243619
|
G | A | 2 | a0001c0001t0002g0216a0001c0001t0002g0218 | 2 | NA18971.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.944-10592G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9243619 | ||||||
| chr18:9243707
|
C | T | 4 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0052others(1): Show | 4 | HG01243.hp1 HG02486.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.944-10504C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9243707 | ||||||
| chr18:9243963
|
G | A | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.944-10248G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9243963 | ||||||
| chr18:9244036
|
A | C | 1 | a0003c0003t0001g0106 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.944-10175A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244036 | ||||||
| chr18:9244066
|
G | A | 1 | a0001c0001t0011g0171 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.944-10145G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244066 | ||||||
| chr18:9244082
|
C | T | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-10129C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244082 | ||||||
| chr18:9244185
|
T | C | 1 | a0001c0001t0005g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.944-10026T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244185 | ||||||
| chr18:9244196
|
G | A | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.944-10015G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244196 | ||||||
| chr18:9244263
|
C | A | 1 | a0001c0010t0002g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.944-9948C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244263 | ||||||
| chr18:9244316
|
T | G | 1 | a0001c0001t0034g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.944-9895T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244316 | ||||||
| chr18:9244532
|
C | G | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-9679C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244532 | ||||||
| chr18:9244548
|
G | A | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-9663G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244548 | ||||||
| chr18:9244713
|
C | T | 1 | a0001c0001t0003g0279 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.944-9498C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244713 | ||||||
| chr18:9244830
|
A | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-9381A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244830 | ||||||
| chr18:9244888
|
T | C | 1 | a0001c0001t0017g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.944-9323T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244888 | ||||||
| chr18:9244939
|
G | T | 1 | a0013c0020t0003g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.944-9272G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244939 | ||||||
| chr18:9244991
|
A | G | 1 | a0001c0001t0010g0227 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.944-9220A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244991 | ||||||
| chr18:9245048
|
A | C | 1 | a0006c0005t0040g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.944-9163A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245048 | ||||||
| chr18:9245366
|
A | G | 317 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.944-8845A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245366 | ||||||
| chr18:9245440
|
A | G | 4 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-8771A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245440 | ||||||
| chr18:9245514
|
G | A | 2 | a0004c0004t0024g0272a0004c0004t0024g0307 | 2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.944-8697G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245514 | ||||||
| chr18:9245623
|
A | G | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.944-8588A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245623 | ||||||
| chr18:9245707
|
T | C | 5 | a0002c0002t0001g0101a0002c0002t0001g0142a0002c0002t0008g0155others(2): Show | 5 | HG00280.hp1 HG00735.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.944-8504T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245707 | ||||||
| chr18:9245883
|
C | T | 1 | a0002c0002t0001g0127 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.944-8328C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245883 | ||||||
| chr18:9245960
|
CTT | C | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-8250_944-8249d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245960 | ||||||
| chr18:9245983
|
G | C | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.944-8228G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245983 | ||||||
| chr18:9246060
|
A | T | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-8151A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246060 | ||||||
| chr18:9246098
|
A | G | 1 | a0002c0002t0025g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.944-8113A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246098 | ||||||
| chr18:9246164
|
CTT | C | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-8044_944-8043d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9246164 | |||||
| chr18:9246326
|
T | C | 174 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.944-7885T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246326 | ||||||
| chr18:9246334
|
T | C | 1 | a0004c0004t0014g0314 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.944-7877T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246334 | ||||||
| chr18:9246380
|
C | T | 217 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.944-7831C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246380 | ||||||
| chr18:9246570
|
G | A | 1 | a0001c0001t0005g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.944-7641G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246570 | ||||||
| chr18:9246665
|
T | G | 1 | a0002c0002t0067g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.944-7546T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246665 | ||||||
| chr18:9246666
|
G | A | 1 | a0007c0027t0004g0309 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.944-7545G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246666 | ||||||
| chr18:9246713
|
A | C | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.944-7498A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246713 | ||||||
| chr18:9246737
|
A | G | 45 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(42): Show | 45 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.944-7474A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246737 | ||||||
| chr18:9246752
|
G | A | 1 | a0001c0001t0034g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.944-7459G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246752 | ||||||
| chr18:9246860
|
C | A | 1 | a0003c0003t0001g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.944-7351C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246860 | ||||||
| chr18:9246898
|
G | A | 217 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.944-7313G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246898 | ||||||
| chr18:9246961
|
T | TAC | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.944-7249_944-7248d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9246961 | |||||
| chr18:9247144
|
TTTTG | T | 27 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(24): Show | 27 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.944-7043_944-7040d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9247144 | |||||
| chr18:9247222
|
TAATCCC | T | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-6986_944-6981d others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9247222 | |||||
| chr18:9247270
|
C | T | 1 | a0002c0002t0001g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.944-6941C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247270 | ||||||
| chr18:9247313
|
C | CA | 42 | a0001c0001t0005g0262a0001c0001t0010g0227a0004c0004t0004g0281others(39): Show | 42 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.944-6882dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9247313 | |||||
| chr18:9247329
|
A | G | 1 | a0003c0003t0001g0093 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.944-6882A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247329 | ||||||
| chr18:9247411
|
C | T | 1 | a0001c0012t0003g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.944-6800C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247411 | ||||||
| chr18:9247459
|
A | G | 1 | a0001c0010t0002g0185 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.944-6752A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247459 | ||||||
| chr18:9247487
|
T | A | 8 | a0002c0002t0001g0013a0002c0002t0001g0123a0002c0002t0001g0133others(5): Show | 8 | NA18941.hp1 NA18971.hp1 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.944-6724T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247487 | ||||||
| chr18:9247494
|
A | T | 3 | a0002c0013t0071g0162a0002c0018t0042g0315a0002c0022t0064g0316 | 3 | HG01106.hp2 HG01167.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.944-6717A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247494 | ||||||
| chr18:9247562
|
T | G | 1 | a0001c0001t0005g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.944-6649T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247562 | ||||||
| chr18:9247604
|
A | T | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-6607A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247604 | ||||||
| chr18:9247782
|
T | TTTTTGTT others(3): Show |
4 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024others(1): Show | 4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-6404_944-6395d others(12): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9247782 | |||||
| chr18:9247782
|
TTTTTG | T | 38 | a0002c0013t0071g0162a0004c0004t0004g0281a0004c0004t0004g0283others(35): Show | 38 | HG00639.hp1 HG01884.hp1 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.944-6399_944-6395d others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9247782 | |||||
| chr18:9247851
|
G | A | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-6360G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247851 | ||||||
| chr18:9247944
|
G | A | 3 | a0002c0013t0071g0162a0002c0018t0042g0315a0002c0022t0064g0316 | 3 | HG01106.hp2 HG01167.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.944-6267G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247944 | ||||||
| chr18:9248152
|
T | C | 170 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.944-6059T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248152 | ||||||
| chr18:9248224
|
G | A | 1 | a0013c0020t0003g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.944-5987G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248224 | ||||||
| chr18:9248297
|
C | T | 1 | a0001c0001t0048g0232 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.944-5914C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248297 | ||||||
| chr18:9248312
|
G | A | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.944-5899G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248312 | ||||||
| chr18:9248359
|
A | G | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-5852A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248359 | ||||||
| chr18:9248466
|
C | T | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.944-5745C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248466 | ||||||
| chr18:9248522
|
G | A | 1 | a0001c0024t0074g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.944-5689G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248522 | ||||||
| chr18:9248584
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-5627T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248584 | ||||||
| chr18:9248616
|
A | G | 3 | a0002c0013t0071g0162a0002c0018t0042g0315a0002c0022t0064g0316 | 3 | HG01106.hp2 HG01167.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.944-5595A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248616 | ||||||
| chr18:9248648
|
A | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.944-5563A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248648 | ||||||
| chr18:9248727
|
A | AAGAC | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-5481_944-5478d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9248727 | |||||
| chr18:9248806
|
A | G | 1 | a0003c0003t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.944-5405A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248806 | ||||||
| chr18:9248929
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-5282T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248929 | ||||||
| chr18:9249001
|
C | T | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.944-5210C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249001 | ||||||
| chr18:9249110
|
G | A | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.944-5101G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249110 | ||||||
| chr18:9249119
|
G | A | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-5092G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249119 | ||||||
| chr18:9249269
|
A | C | 2 | a0001c0001t0002g0278a0001c0001t0003g0279 | 2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.944-4942A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249269 | ||||||
| chr18:9249468
|
G | T | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-4743G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249468 | ||||||
| chr18:9249591
|
C | T | 1 | a0003c0003t0001g0146 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.944-4620C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249591 | ||||||
| chr18:9249660
|
T | C | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.944-4551T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249660 | ||||||
| chr18:9249844
|
T | C | 43 | a0002c0013t0071g0162a0002c0018t0042g0315a0002c0022t0064g0316others(40): Show | 43 | HG00140.hp1 HG00639.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.944-4367T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249844 | ||||||
| chr18:9249945
|
CTG | C | 4 | a0004c0004t0004g0292a0004c0004t0004g0300a0004c0004t0036g0293others(1): Show | 4 | NA18967.hp1 NA18973.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-4263_944-4262d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9249945 | |||||
| chr18:9250011
|
G | A | 2 | a0001c0001t0027g0065a0001c0001t0027g0131 | 2 | HG01123.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.944-4200G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250011 | ||||||
| chr18:9250057
|
A | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.944-4154A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250057 | ||||||
| chr18:9250377
|
A | G | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.944-3834A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250377 | ||||||
| chr18:9250382
|
G | A | 1 | a0004c0004t0018g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.944-3829G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250382 | ||||||
| chr18:9250418
|
G | A | 1 | a0001c0001t0046g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.944-3793G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250418 | ||||||
| chr18:9250499
|
A | G | 217 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.944-3712A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250499 | ||||||
| chr18:9250538
|
G | A | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.944-3673G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250538 | ||||||
| chr18:9250545
|
C | G | 1 | a0001c0001t0017g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.944-3666C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250545 | ||||||
| chr18:9250743
|
C | G | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-3468C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250743 | ||||||
| chr18:9250915
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-3296T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250915 | ||||||
| chr18:9250918
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-3293T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250918 | ||||||
| chr18:9250970
|
G | C | 2 | a0002c0002t0001g0127a0002c0002t0008g0126 | 2 | HG03942.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.944-3241G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250970 | ||||||
| chr18:9251025
|
T | C | 1 | a0002c0002t0006g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.944-3186T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251025 | ||||||
| chr18:9251027
|
T | A | 1 | a0002c0002t0006g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.944-3184T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251027 | ||||||
| chr18:9251080
|
A | G | 1 | a0004c0004t0004g0300 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.944-3131A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251080 | ||||||
| chr18:9251113
|
A | G | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-3098A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251113 | ||||||
| chr18:9251221
|
G | A | 2 | a0004c0004t0004g0290a0004c0004t0004g0304 | 2 | NA18997.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.944-2990G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251221 | ||||||
| chr18:9251238
|
C | T | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.944-2973C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251238 | ||||||
| chr18:9251259
|
C | A | 1 | a0002c0002t0006g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.944-2952C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251259 | ||||||
| chr18:9251569
|
G | A | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-2642G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251569 | ||||||
| chr18:9251613
|
G | T | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-2598G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251613 | ||||||
| chr18:9251666
|
C | T | 2 | a0001c0001t0003g0259a0001c0001t0003g0263 | 2 | HG00735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.944-2545C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251666 | ||||||
| chr18:9251803
|
A | T | 2 | a0004c0004t0004g0292a0004c0004t0036g0293 | 2 | NA18973.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.944-2408A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251803 | ||||||
| chr18:9251817
|
C | T | 2 | a0001c0001t0027g0065a0001c0001t0027g0131 | 2 | HG01123.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.944-2394C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251817 | ||||||
| chr18:9252260
|
G | A | 8 | a0001c0001t0017g0015a0001c0001t0017g0021a0001c0001t0017g0028others(5): Show | 8 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.944-1951G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9252260 | ||||||
| chr18:9252498
|
A | G | 1 | a0003c0003t0008g0084 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.944-1713A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9252498 | ||||||
| chr18:9252499
|
T | C | 2 | a0002c0002t0001g0135a0002c0002t0001g0136 | 2 | HG02129.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.944-1712T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9252499 | ||||||
| chr18:9252539
|
G | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-1672G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9252539 | ||||||
| chr18:9252751
|
G | A | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.944-1460G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9252751 | ||||||
| chr18:9252808
|
A | G | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-1403A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9252808 | ||||||
| chr18:9253004
|
T | TTA | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-1198_944-1197d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9253004 | |||||
| chr18:9253084
|
T | C | 1 | a0003c0003t0065g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.944-1127T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253084 | ||||||
| chr18:9253114
|
G | A | 2 | a0001c0001t0016g0184a0001c0001t0016g0277 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.944-1097G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253114 | ||||||
| chr18:9253157
|
A | G | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-1054A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253157 | ||||||
| chr18:9253298
|
C | T | 1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.944-913C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253298 | ||||||
| chr18:9253415
|
A | G | 1 | a0003c0003t0065g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.944-796A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253415 | ||||||
| chr18:9253474
|
G | A | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | NA18955.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.944-737G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253474 | ||||||
| chr18:9253744
|
G | A | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-467G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253744 | ||||||
| chr18:9253914
|
A | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.944-297A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253914 | ||||||
| chr18:9253945
|
T | C | 3 | a0001c0001t0017g0029a0001c0001t0034g0030a0001c0001t0034g0031 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.944-266T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253945 | ||||||
| chr18:9259000
|
C | T | 1 | a0004c0004t0004g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.5664+69C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259000 | ||||||
| chr18:9259142
|
A | G | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5664+211A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259142 | ||||||
| chr18:9259172
|
G | C | 174 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.5664+241G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259172 | ||||||
| chr18:9259220
|
T | TCC | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5664+290_5664+291i others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9259220 | |||||
| chr18:9259222
|
A | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5664+291A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259222 | ||||||
| chr18:9259290
|
T | C | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5664+359T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259290 | ||||||
| chr18:9259368
|
T | C | 148 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.5664+437T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259368 | ||||||
| chr18:9259370
|
C | T | 1 | a0002c0002t0001g0116 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5664+439C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259370 | ||||||
| chr18:9259386
|
A | AACACATT others(16): Show |
3 | a0002c0002t0001g0110a0002c0022t0064g0316a0007c0027t0004g0309 | 3 | HG00639.hp1 HG01167.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.5664+496_5664+518d others(25): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9259386 | |||||
| chr18:9259386
|
AACACATT others(16): Show |
A | 6 | a0002c0002t0008g0155a0006c0005t0015g0006a0006c0005t0015g0007others(3): Show | 6 | HG01069.hp2 HG01884.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5664+496_5664+518d others(25): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9259386 | |||||
| chr18:9259396
|
T | C | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.5664+465T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259396 | ||||||
| chr18:9259434
|
C | T | 3 | a0002c0002t0001g0070a0002c0002t0001g0080a0012c0016t0001g0079 | 3 | HG01109.hp1 HG01168.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.5664+503C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259434 | ||||||
| chr18:9259452
|
A | G | 2 | a0002c0002t0001g0119a0002c0025t0001g0120 | 2 | HG01167.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5664+521A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259452 | ||||||
| chr18:9259549
|
T | A | 1 | a0002c0002t0009g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5664+618T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259549 | ||||||
| chr18:9259721
|
A | G | 1 | a0002c0002t0013g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5664+790A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259721 | ||||||
| chr18:9259805
|
T | A | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5664+874T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259805 | ||||||
| chr18:9259894
|
A | G | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5664+963A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259894 | ||||||
| chr18:9260012
|
C | T | 1 | a0003c0003t0065g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5664+1081C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260012 | ||||||
| chr18:9260171
|
C | T | 1 | a0004c0004t0004g0288 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.5664+1240C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260171 | ||||||
| chr18:9260212
|
C | T | 1 | a0002c0015t0006g0047 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5664+1281C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260212 | ||||||
| chr18:9260218
|
A | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5664+1287A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260218 | ||||||
| chr18:9260248
|
G | A | 5 | a0001c0001t0002g0188a0001c0001t0002g0273a0001c0001t0002g0274others(2): Show | 5 | HG01123.hp2 HG01934.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.5664+1317G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260248 | ||||||
| chr18:9260855
|
T | G | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5664+1924T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260855 | ||||||
| chr18:9260870
|
C | T | 26 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(23): Show | 26 | HG00639.hp1 HG01934.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.5664+1939C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260870 | ||||||
| chr18:9260877
|
C | G | 1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5664+1946C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260877 | ||||||
| chr18:9260994
|
C | T | 2 | a0003c0003t0062g0072a0003c0003t0063g0071 | 2 | NA19057.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.5664+2063C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260994 | ||||||
| chr18:9261021
|
T | C | 7 | a0001c0009t0033g0019a0001c0009t0033g0020a0006c0005t0015g0006others(4): Show | 7 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.5664+2090T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9261021 | ||||||
| chr18:9261715
|
T | G | 2 | a0001c0001t0034g0030a0001c0001t0034g0031 | 2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5665-2075T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9261715 | ||||||
| chr18:9261720
|
C | T | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5665-2070C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9261720 | ||||||
| chr18:9261781
|
G | A | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5665-2009G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9261781 | ||||||
| chr18:9261806
|
T | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5665-1984T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9261806 | ||||||
| chr18:9261991
|
G | A | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5665-1799G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9261991 | ||||||
| chr18:9262055
|
G | A | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5665-1735G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262055 | ||||||
| chr18:9262103
|
T | C | 2 | a0004c0004t0024g0272a0004c0004t0024g0307 | 2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.5665-1687T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262103 | ||||||
| chr18:9262110
|
T | G | 1 | a0004c0004t0004g0281 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.5665-1680T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262110 | ||||||
| chr18:9262264
|
G | A | 1 | a0001c0001t0002g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5665-1526G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262264 | ||||||
| chr18:9262720
|
A | G | 1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5665-1070A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262720 | ||||||
| chr18:9262727
|
T | G | 1 | a0003c0003t0060g0098 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.5665-1063T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262727 | ||||||
| chr18:9262781
|
A | T | 1 | a0001c0001t0002g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.5665-1009A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262781 | ||||||
| chr18:9262786
|
C | CT | 67 | a0001c0001t0002g0064a0001c0001t0002g0188a0001c0001t0002g0194others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.5665-1004_5665-100 others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262786 | ||||||
| chr18:9262786
|
C | CTT | 40 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0201others(37): Show | 40 | HG00733.hp1 HG00735.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.5665-1004_5665-100 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262786 | ||||||
| chr18:9262786
|
C | CTTT | 7 | a0001c0001t0003g0001a0001c0001t0011g0171a0001c0001t0030g0276others(4): Show | 7 | HG01952.hp1 HG02148.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.5665-1004_5665-100 others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262786 | ||||||
| chr18:9262786
|
C | CTTTT | 8 | a0001c0001t0003g0045a0001c0001t0003g0173a0001c0001t0003g0251others(5): Show | 8 | HG01884.hp2 HG02300.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.5665-1004_5665-100 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262786 | ||||||
| chr18:9262787
|
C | CT | 91 | a0001c0001t0009g0023a0001c0001t0009g0024a0001c0001t0066g0102others(88): Show | 91 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.5665-974dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9262787 | |||||
| chr18:9262787
|
C | CTT | 25 | a0001c0001t0034g0031a0002c0002t0001g0123a0002c0002t0008g0126others(22): Show | 25 | HG01361.hp1 HG01934.hp2 HG02523.hp1 others(22): Show |
intron_variant | MODIFIER | c.5665-975_5665-974d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9262787 | |||||
| chr18:9262787
|
C | CTTTTTTT others(5): Show |
1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5665-985_5665-974d others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9262787 | |||||
| chr18:9262787
|
C | T | 129 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.5665-1003C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262787 | ||||||
| chr18:9262787
|
CT | C | 22 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(19): Show | 22 | HG00140.hp2 HG00733.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.5665-974delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9262787 | |||||
| chr18:9262787
|
CTTTTTTT others(3): Show |
C | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5665-983_5665-974d others(12): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9262787 | |||||
| chr18:9262829
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5665-961C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262829 | ||||||
| chr18:9262830
|
G | A | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5665-960G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262830 | ||||||
| chr18:9263028
|
C | A | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5665-762C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9263028 | ||||||
| chr18:9263156
|
C | T | 1 | a0014c0021t0003g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5665-634C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9263156 | ||||||
| chr18:9263399
|
AC | A | 125 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5665-390delC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9263399 | ||||||
| chr18:9263414
|
A | G | 2 | a0002c0002t0061g0130a0010c0023t0035g0061 | 2 | HG02976.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.5665-376A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9263414 | ||||||
| chr18:9263457
|
A | G | 1 | a0001c0001t0049g0180 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5665-333A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9263457 | ||||||
| chr18:9263580
|
T | C | 5 | a0002c0002t0006g0053a0002c0002t0006g0055a0002c0002t0019g0056others(2): Show | 5 | HG00140.hp2 HG01070.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.5665-210T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9263580 | ||||||
| chr18:9263943
|
A | C | 1 | a0003c0003t0001g0106 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5763+55A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9263943 | ||||||
| chr18:9264265
|
C | T | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+377C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264265 | ||||||
| chr18:9264290
|
C | T | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5763+402C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264290 | ||||||
| chr18:9264349
|
T | C | 3 | a0001c0001t0017g0021a0001c0001t0017g0028a0015c0019t0070g0266 | 3 | HG02965.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5763+461T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264349 | ||||||
| chr18:9264428
|
G | T | 1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.5763+540G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264428 | ||||||
| chr18:9264490
|
G | A | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5763+602G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264490 | ||||||
| chr18:9264517
|
A | C | 2 | a0001c0001t0021g0257a0001c0001t0052g0256 | 2 | NA19009.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.5763+629A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264517 | ||||||
| chr18:9264521
|
AT | A | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5763+637delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9264521 | |||||
| chr18:9264553
|
T | A | 3 | a0001c0001t0017g0029a0001c0001t0034g0030a0001c0001t0034g0031 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5763+665T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264553 | ||||||
| chr18:9264595
|
T | C | 1 | a0002c0002t0059g0129 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.5763+707T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264595 | ||||||
| chr18:9264680
|
C | G | 1 | a0002c0002t0001g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5763+792C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264680 | ||||||
| chr18:9264692
|
A | G | 5 | a0001c0009t0033g0019a0001c0009t0033g0020a0002c0013t0071g0162others(2): Show | 5 | HG01106.hp2 HG01167.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.5763+804A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264692 | ||||||
| chr18:9264719
|
C | T | 1 | a0004c0004t0018g0299 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.5763+831C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264719 | ||||||
| chr18:9264766
|
AT | A | 72 | a0001c0009t0033g0019a0001c0009t0033g0020a0002c0002t0006g0037others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.5763+880delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9264766 | |||||
| chr18:9264785
|
C | T | 1 | a0002c0002t0006g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5763+897C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264785 | ||||||
| chr18:9264900
|
C | T | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5763+1012C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264900 | ||||||
| chr18:9264984
|
C | T | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5763+1096C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264984 | ||||||
| chr18:9265012
|
G | A | 2 | a0001c0001t0007g0189a0001c0001t0007g0240 | 2 | HG00733.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.5763+1124G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265012 | ||||||
| chr18:9265078
|
AG | A | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+1194delG | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9265078 | |||||
| chr18:9265184
|
A | G | 145 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.5763+1296A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265184 | ||||||
| chr18:9265293
|
A | G | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+1405A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265293 | ||||||
| chr18:9265372
|
C | T | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5763+1484C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265372 | ||||||
| chr18:9265430
|
TC | T | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5763+1544delC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9265430 | |||||
| chr18:9265474
|
C | T | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5763+1586C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265474 | ||||||
| chr18:9265560
|
G | A | 1 | a0007c0027t0004g0309 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5763+1672G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265560 | ||||||
| chr18:9265727
|
A | G | 1 | a0003c0003t0001g0106 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5763+1839A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265727 | ||||||
| chr18:9265784
|
G | A | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5763+1896G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265784 | ||||||
| chr18:9265797
|
A | G | 1 | a0001c0001t0005g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5763+1909A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265797 | ||||||
| chr18:9265798
|
A | C | 1 | a0001c0001t0005g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5763+1910A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265798 | ||||||
| chr18:9265813
|
A | C | 1 | a0003c0003t0008g0105 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.5763+1925A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265813 | ||||||
| chr18:9265822
|
C | T | 38 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(35): Show | 38 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.5763+1934C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265822 | ||||||
| chr18:9265823
|
G | A | 3 | a0001c0001t0017g0021a0001c0001t0017g0028a0015c0019t0070g0266 | 3 | HG02965.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5763+1935G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265823 | ||||||
| chr18:9265955
|
C | T | 4 | a0001c0001t0017g0029a0001c0001t0031g0248a0001c0001t0034g0030others(1): Show | 4 | HG01515.hp2 HG02055.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.5763+2067C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265955 | ||||||
| chr18:9266081
|
A | G | 1 | a0002c0002t0006g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5763+2193A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266081 | ||||||
| chr18:9266084
|
C | T | 2 | a0001c0001t0007g0189a0001c0001t0007g0240 | 2 | HG00733.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.5763+2196C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266084 | ||||||
| chr18:9266177
|
G | A | 1 | a0008c0026t0039g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5763+2289G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266177 | ||||||
| chr18:9266284
|
T | C | 3 | a0001c0001t0003g0172a0001c0001t0011g0171a0001c0001t0022g0170 | 3 | HG01361.hp2 HG01952.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.5763+2396T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266284 | ||||||
| chr18:9266373
|
T | C | 1 | a0002c0002t0025g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5763+2485T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266373 | ||||||
| chr18:9266378
|
T | C | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5763+2490T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266378 | ||||||
| chr18:9266439
|
A | G | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5763+2551A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266439 | ||||||
| chr18:9266506
|
C | T | 1 | a0001c0001t0056g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5763+2618C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266506 | ||||||
| chr18:9266627
|
A | G | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5763+2739A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266627 | ||||||
| chr18:9266640
|
C | T | 42 | a0001c0009t0033g0019a0001c0009t0033g0020a0004c0004t0004g0281others(39): Show | 42 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.5763+2752C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266640 | ||||||
| chr18:9266791
|
T | C | 3 | a0001c0001t0017g0029a0001c0001t0034g0030a0001c0001t0034g0031 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5763+2903T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266791 | ||||||
| chr18:9266826
|
T | G | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5763+2938T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266826 | ||||||
| chr18:9266845
|
C | T | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5763+2957C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266845 | ||||||
| chr18:9266860
|
T | C | 2 | a0001c0001t0034g0030a0001c0001t0034g0031 | 2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5763+2972T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266860 | ||||||
| chr18:9266946
|
A | T | 1 | a0002c0002t0006g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5763+3058A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266946 | ||||||
| chr18:9266975
|
T | G | 1 | a0003c0003t0001g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.5763+3087T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266975 | ||||||
| chr18:9266990
|
G | T | 9 | a0001c0001t0012g0192a0001c0001t0012g0196a0001c0001t0012g0210others(6): Show | 9 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.5763+3102G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266990 | ||||||
| chr18:9267149
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+3261T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267149 | ||||||
| chr18:9267214
|
C | G | 3 | a0001c0001t0017g0021a0001c0001t0017g0028a0015c0019t0070g0266 | 3 | HG02965.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5763+3326C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267214 | ||||||
| chr18:9267237
|
C | A | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5763+3349C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267237 | ||||||
| chr18:9267275
|
T | C | 5 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5763+3387T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267275 | ||||||
| chr18:9267329
|
C | T | 1 | a0002c0022t0064g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5763+3441C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267329 | ||||||
| chr18:9267387
|
G | C | 1 | a0001c0001t0017g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5763+3499G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267387 | ||||||
| chr18:9267394
|
G | A | 1 | a0001c0001t0017g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5763+3506G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267394 | ||||||
| chr18:9267400
|
A | G | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.5763+3512A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267400 | ||||||
| chr18:9267501
|
C | T | 3 | a0001c0001t0017g0029a0001c0001t0034g0030a0001c0001t0034g0031 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5763+3613C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267501 | ||||||
| chr18:9267505
|
C | T | 1 | a0004c0004t0014g0312 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5763+3617C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267505 | ||||||
| chr18:9267593
|
A | G | 5 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5763+3705A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267593 | ||||||
| chr18:9267595
|
C | T | 5 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5763+3707C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267595 | ||||||
| chr18:9267611
|
C | T | 7 | a0003c0003t0001g0083a0003c0003t0001g0088a0003c0003t0023g0010others(4): Show | 7 | HG00323.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.5763+3723C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267611 | ||||||
| chr18:9267791
|
T | G | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5763+3903T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267791 | ||||||
| chr18:9267870
|
A | G | 130 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.5763+3982A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267870 | ||||||
| chr18:9267915
|
C | T | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5763+4027C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267915 | ||||||
| chr18:9267916
|
G | A | 2 | a0001c0001t0017g0021a0001c0001t0017g0028 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5763+4028G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267916 | ||||||
| chr18:9268083
|
C | T | 1 | a0002c0002t0001g0070 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.5763+4195C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268083 | ||||||
| chr18:9268173
|
A | G | 72 | a0001c0009t0033g0019a0001c0009t0033g0020a0002c0002t0006g0037others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.5763+4285A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268173 | ||||||
| chr18:9268174
|
G | A | 72 | a0001c0009t0033g0019a0001c0009t0033g0020a0002c0002t0006g0037others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.5763+4286G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268174 | ||||||
| chr18:9268224
|
T | C | 6 | a0002c0002t0006g0053a0002c0002t0006g0054a0002c0002t0006g0055others(3): Show | 6 | HG00140.hp2 HG01070.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.5763+4336T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268224 | ||||||
| chr18:9268252
|
T | C | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5763+4364T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268252 | ||||||
| chr18:9268471
|
G | A | 1 | a0001c0001t0005g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5763+4583G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268471 | ||||||
| chr18:9268497
|
A | G | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5763+4609A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268497 | ||||||
| chr18:9268573
|
C | T | 1 | a0001c0001t0003g0271 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5763+4685C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268573 | ||||||
| chr18:9268615
|
T | C | 217 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.5763+4727T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268615 | ||||||
| chr18:9268616
|
G | A | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5763+4728G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268616 | ||||||
| chr18:9268641
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+4753T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268641 | ||||||
| chr18:9268642
|
A | G | 1 | a0001c0001t0031g0317 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.5763+4754A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268642 | ||||||
| chr18:9268700
|
G | T | 1 | a0015c0019t0070g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5763+4812G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268700 | ||||||
| chr18:9268701
|
A | T | 1 | a0015c0019t0070g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5763+4813A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268701 | ||||||
| chr18:9268725
|
T | A | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+4837T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268725 | ||||||
| chr18:9268764
|
G | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5763+4876G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268764 | ||||||
| chr18:9268884
|
G | A | 1 | a0003c0003t0001g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.5763+4996G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268884 | ||||||
| chr18:9268921
|
A | G | 1 | a0003c0003t0001g0085 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.5763+5033A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268921 | ||||||
| chr18:9268938
|
A | G | 4 | a0001c0001t0022g0002a0001c0001t0022g0005a0001c0001t0054g0003others(1): Show | 4 | HG00639.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5763+5050A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268938 | ||||||
| chr18:9268957
|
G | A | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+5069G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268957 | ||||||
| chr18:9269068
|
G | A | 1 | a0004c0004t0024g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5763+5180G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269068 | ||||||
| chr18:9269077
|
C | T | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5763+5189C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269077 | ||||||
| chr18:9269135
|
A | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5763+5247A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269135 | ||||||
| chr18:9269162
|
G | A | 3 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5763+5274G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269162 | ||||||
| chr18:9269222
|
C | T | 34 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(31): Show | 34 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.5763+5334C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269222 | ||||||
| chr18:9269346
|
A | G | 1 | a0004c0004t0004g0302 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.5763+5458A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269346 | ||||||
| chr18:9269390
|
CA | C | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5763+5506delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9269390 | |||||
| chr18:9269484
|
A | T | 4 | a0001c0001t0002g0215a0001c0001t0002g0216a0001c0001t0002g0218others(1): Show | 4 | NA18971.hp2 NA18982.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.5763+5596A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269484 | ||||||
| chr18:9269540
|
A | C | 130 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.5763+5652A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269540 | ||||||
| chr18:9269591
|
C | T | 1 | a0001c0001t0003g0193 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.5763+5703C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269591 | ||||||
| chr18:9269660
|
A | G | 130 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.5763+5772A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269660 | ||||||
| chr18:9269843
|
ATGGGAGA others(4): Show |
A | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5764-5679_5764-566 others(15): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9269843 | |||||
| chr18:9269907
|
C | G | 2 | a0002c0002t0001g0157a0002c0002t0008g0159 | 2 | NA18979.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.5764-5617C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269907 | ||||||
| chr18:9270090
|
G | A | 8 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024others(5): Show | 8 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.5764-5434G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270090 | ||||||
| chr18:9270243
|
C | T | 1 | a0004c0004t0024g0307 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5764-5281C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270243 | ||||||
| chr18:9270409
|
T | C | 1 | a0003c0003t0001g0014 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.5764-5115T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270409 | ||||||
| chr18:9270415
|
G | A | 4 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.5764-5109G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270415 | ||||||
| chr18:9270604
|
A | G | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5764-4920A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270604 | ||||||
| chr18:9270643
|
C | T | 5 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0173others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.5764-4881C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270643 | ||||||
| chr18:9270726
|
C | T | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5764-4798C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270726 | ||||||
| chr18:9270746
|
C | T | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5764-4778C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270746 | ||||||
| chr18:9270792
|
T | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5764-4732T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270792 | ||||||
| chr18:9270816
|
A | T | 1 | a0001c0001t0056g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5764-4708A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270816 | ||||||
| chr18:9270859
|
T | C | 1 | a0004c0004t0004g0300 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5764-4665T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270859 | ||||||
| chr18:9271381
|
C | T | 1 | a0001c0001t0017g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5764-4143C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9271381 | ||||||
| chr18:9271400
|
G | A | 1 | a0002c0002t0069g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5764-4124G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9271400 | ||||||
| chr18:9271532
|
T | A | 312 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(309): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.5764-3992T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9271532 | ||||||
| chr18:9271666
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5764-3858T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9271666 | ||||||
| chr18:9271745
|
T | G | 4 | a0002c0002t0006g0039a0002c0002t0006g0050a0002c0002t0006g0051others(1): Show | 4 | HG00733.hp2 HG01255.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.5764-3779T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9271745 | ||||||
| chr18:9271825
|
T | C | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5764-3699T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9271825 | ||||||
| chr18:9272022
|
C | T | 5 | a0002c0002t0013g0069a0002c0002t0013g0114a0002c0002t0013g0115others(2): Show | 5 | HG02895.hp2 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.5764-3502C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272022 | ||||||
| chr18:9272066
|
A | G | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5764-3458A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272066 | ||||||
| chr18:9272101
|
A | G | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5764-3423A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272101 | ||||||
| chr18:9272301
|
G | A | 1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5764-3223G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272301 | ||||||
| chr18:9272430
|
T | C | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5764-3094T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272430 | ||||||
| chr18:9272494
|
G | A | 1 | a0001c0001t0012g0192 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5764-3030G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272494 | ||||||
| chr18:9272644
|
G | A | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5764-2880G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272644 | ||||||
| chr18:9272655
|
A | G | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5764-2869A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272655 | ||||||
| chr18:9272813
|
A | G | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5764-2711A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272813 | ||||||
| chr18:9272868
|
A | G | 1 | a0003c0003t0062g0072 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.5764-2656A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272868 | ||||||
| chr18:9272936
|
G | A | 2 | a0001c0001t0009g0022a0001c0001t0009g0023 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5764-2588G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272936 | ||||||
| chr18:9272943
|
G | A | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5764-2581G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272943 | ||||||
| chr18:9272958
|
C | CATG | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5764-2566_5764-256 others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272958 | ||||||
| chr18:9273034
|
G | A | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5764-2490G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9273034 | ||||||
| chr18:9273382
|
C | G | 2 | a0001c0001t0017g0015a0001c0024t0074g0018 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5764-2142C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9273382 | ||||||
| chr18:9273388
|
G | T | 2 | a0001c0001t0017g0015a0001c0024t0074g0018 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5764-2136G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9273388 | ||||||
| chr18:9273398
|
A | G | 3 | a0002c0002t0001g0150a0002c0002t0001g0151a0002c0002t0008g0149 | 3 | HG02258.hp2 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5764-2126A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9273398 | ||||||
| chr18:9273541
|
G | T | 1 | a0001c0001t0005g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.5764-1983G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9273541 | ||||||
| chr18:9273789
|
C | G | 1 | a0001c0001t0003g0242 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.5764-1735C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9273789 | ||||||
| chr18:9274149
|
G | A | 1 | a0001c0001t0005g0220 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5764-1375G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274149 | ||||||
| chr18:9274234
|
A | G | 1 | a0006c0005t0015g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5764-1290A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274234 | ||||||
| chr18:9274299
|
A | G | 1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5764-1225A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274299 | ||||||
| chr18:9274577
|
G | C | 1 | a0001c0001t0005g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5764-947G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274577 | ||||||
| chr18:9274638
|
A | G | 217 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.5764-886A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274638 | ||||||
| chr18:9274649
|
A | G | 1 | a0004c0004t0004g0300 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5764-875A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274649 | ||||||
| chr18:9274923
|
C | T | 1 | a0005c0006t0007g0204 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.5764-601C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274923 | ||||||
| chr18:9275173
|
A | T | 1 | a0004c0004t0004g0304 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.5764-351A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9275173 | ||||||
| chr18:9275303
|
A | AAT | 58 | a0001c0001t0002g0201a0001c0001t0003g0172a0001c0001t0003g0193others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.5764-208_5764-207d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9275303 | |||||
| chr18:9275316
|
A | T | 9 | a0001c0001t0002g0194a0001c0001t0002g0195a0001c0001t0009g0022others(6): Show | 9 | HG00639.hp2 HG02055.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.5764-208A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9275316 | ||||||
| chr18:9275366
|
C | T | 8 | a0001c0001t0017g0015a0001c0001t0017g0021a0001c0001t0017g0028others(5): Show | 8 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.5764-158C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9275366 | ||||||
| chr18:9275744
|
TAGAA | T | 15 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.5907+82_5907+85del others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9275744 | |||||
| chr18:9275844
|
G | A | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5907+177G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9275844 | ||||||
| chr18:9276191
|
G | T | 72 | a0001c0009t0033g0019a0001c0009t0033g0020a0002c0002t0006g0037others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.5907+524G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276191 | ||||||
| chr18:9276245
|
TAAAC | T | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5907+580_5907+583d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9276245 | |||||
| chr18:9276265
|
C | G | 23 | a0002c0002t0006g0037a0002c0002t0006g0038a0002c0002t0006g0039others(20): Show | 23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.5907+598C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276265 | ||||||
| chr18:9276408
|
A | G | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5907+741A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276408 | ||||||
| chr18:9276495
|
C | T | 5 | a0003c0003t0001g0014a0003c0003t0001g0085a0003c0003t0001g0108others(2): Show | 5 | HG00609.hp1 HG00621.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.5907+828C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276495 | ||||||
| chr18:9276509
|
T | G | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5907+842T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276509 | ||||||
| chr18:9276617
|
G | A | 1 | a0001c0001t0017g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5907+950G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276617 | ||||||
| chr18:9276712
|
C | CA | 15 | a0001c0001t0020g0182a0001c0001t0020g0183a0001c0001t0020g0197others(12): Show | 15 | HG01106.hp1 HG01433.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.5907+1054dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9276712 | |||||
| chr18:9276726
|
A | G | 1 | a0001c0001t0005g0217 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.5907+1059A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276726 | ||||||
| chr18:9276806
|
G | T | 1 | a0001c0001t0066g0102 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5907+1139G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276806 | ||||||
| chr18:9276936
|
C | G | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5907+1269C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276936 | ||||||
| chr18:9277083
|
C | T | 1 | a0004c0004t0004g0286 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.5907+1416C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277083 | ||||||
| chr18:9277104
|
T | C | 4 | a0001c0007t0028g0025a0001c0007t0028g0026a0001c0007t0053g0027others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5907+1437T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277104 | ||||||
| chr18:9277116
|
T | C | 2 | a0002c0002t0032g0160a0002c0002t0032g0161 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5907+1449T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277116 | ||||||
| chr18:9277181
|
A | T | 4 | a0001c0001t0011g0241a0001c0001t0011g0245a0001c0001t0011g0247others(1): Show | 4 | HG00423.hp2 HG00621.hp2 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.5907+1514A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277181 | ||||||
| chr18:9277321
|
C | CT | 41 | a0001c0001t0002g0268a0001c0001t0003g0251a0001c0001t0003g0271others(38): Show | 41 | HG00733.hp2 HG01069.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.5907+1679dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9277321 | |||||
| chr18:9277321
|
C | CTT | 34 | a0002c0002t0006g0052a0002c0002t0025g0036a0002c0002t0025g0060others(31): Show | 34 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.5907+1678_5907+167 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9277321 | |||||
| chr18:9277321
|
CT | C | 6 | a0001c0001t0009g0023a0001c0001t0056g0174a0002c0002t0001g0094others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.5907+1679delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9277321 | |||||
| chr18:9277527
|
C | A | 146 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.5907+1860C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277527 | ||||||
| chr18:9277540
|
G | T | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5907+1873G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277540 | ||||||
| chr18:9277549
|
G | T | 1 | a0001c0001t0002g0188 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.5907+1882G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277549 | ||||||
| chr18:9277706
|
GAGGTGGG others(105): Show |
G | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5908-1838_5908-172 others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9277706 | |||||
| chr18:9278180
|
T | G | 2 | a0004c0004t0024g0272a0004c0004t0024g0307 | 2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.5908-1369T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278180 | ||||||
| chr18:9278182
|
T | C | 72 | a0001c0009t0033g0019a0001c0009t0033g0020a0002c0002t0006g0037others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.5908-1367T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278182 | ||||||
| chr18:9278204
|
A | T | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5908-1345A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278204 | ||||||
| chr18:9278250
|
GT | G | 72 | a0001c0009t0033g0019a0001c0009t0033g0020a0002c0002t0006g0037others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.5908-1297delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9278250 | |||||
| chr18:9278482
|
A | G | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5908-1067A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278482 | ||||||
| chr18:9278556
|
T | C | 40 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(37): Show | 40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5908-993T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278556 | ||||||
| chr18:9278744
|
T | A | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5908-805T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278744 | ||||||
| chr18:9278906
|
T | C | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5908-643T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278906 | ||||||
| chr18:9279012
|
C | T | 1 | a0002c0018t0042g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5908-537C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9279012 | ||||||
| chr18:9279082
|
TAAAGAAT others(11): Show |
T | 317 | a0001c0001t0002g0064a0001c0001t0002g0067a0001c0001t0002g0068others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.5908-448_5908-431d others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9279082 | |||||
| chr18:9279130
|
T | C | 5 | a0005c0006t0007g0176a0005c0006t0007g0178a0005c0006t0007g0179others(2): Show | 5 | HG00099.hp1 HG01255.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.5908-419T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9279130 | ||||||
| chr18:9279344
|
C | T | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040 | 3 | HG01891.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5908-205C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9279344 | ||||||
| chr18:9279526
|
T | C | 35 | a0004c0004t0004g0281a0004c0004t0004g0283a0004c0004t0004g0284others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5908-23T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9279526 | ||||||
| chr18:9279690
|
T | TA | 6 | a0001c0010t0002g0175a0001c0010t0002g0185a0002c0002t0032g0160others(3): Show | 6 | HG01891.hp2 HG02683.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.6003+60dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | 9279690 | |||||
| chr18:9279690
|
TA | T | 42 | a0001c0001t0002g0199a0001c0001t0005g0225a0001c0001t0005g0228others(39): Show | 42 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(39): Show |
intron_variant | MODIFIER | c.6003+60delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | 9279690 | |||||
| chr18:9279706
|
T | A | 1 | a0010c0023t0035g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6003+62T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9279706 | ||||||
| chr18:9279753
|
A | G | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6003+109A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9279753 | ||||||
| chr18:9279763
|
C | G | 2 | a0001c0009t0033g0019a0001c0009t0033g0020 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6003+119C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9279763 | ||||||
| chr18:9279860
|
T | C | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6003+216T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9279860 | ||||||
| chr18:9279970
|
A | G | 3 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0024 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.6003+326A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9279970 | ||||||
| chr18:9280040
|
T | A | 5 | a0006c0005t0015g0006a0006c0005t0015g0007a0006c0005t0015g0008others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.6003+396T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280040 | ||||||
| chr18:9280047
|
A | T | 3 | a0002c0002t0032g0160a0002c0002t0032g0161a0002c0002t0043g0040 | 3 | HG01891.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.6003+403A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280047 | ||||||
| chr18:9280133
|
A | G | 1 | a0002c0002t0043g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.6003+489A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280133 | ||||||
| chr18:9280310
|
G | T | 2 | a0001c0001t0003g0193a0001c0001t0003g0198 | 2 | HG01123.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.6004-631G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280310 | ||||||
| chr18:9280327
|
A | G | 2 | a0001c0001t0002g0064a0001c0001t0002g0268 | 2 | HG02738.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.6004-614A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280327 | ||||||
| chr18:9280356
|
G | A | 1 | a0006c0005t0015g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6004-585G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280356 | ||||||
| chr18:9280735
|
G | A | 1 | a0002c0013t0071g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6004-206G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280735 |