| geneid | 580 |
|---|---|
| ensemblid | ENSG00000138376.11 |
| hgncid | 952 |
| symbol | BARD1 |
| name | BRCA1 associated RING domain 1 |
| refseq_nuc | NM_000465.4 |
| refseq_prot | NP_000456.2 |
| ensembl_nuc | ENST00000260947.9 |
| ensembl_prot | ENSP00000260947.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 214725646 |
| end | 214809683 |
| strand | - |
| ver | v1.2 |
| region | chr2:214725646-214809683 |
| region5000 | chr2:214720646-214814683 |
| regionname0 | BARD1_chr2_214725646_214809683 |
| regionname5000 | BARD1_chr2_214720646_214814683 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 777 | 164 | 37 | 22 | 81 | 3 | 19 | 63 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002 | 0/0 | 777 | 89 | 10 | 20 | 43 | 4 | 12 | 30 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0003 | 0/0 | 770 | 23 | 1 | 4 | 13 | 0 | 5 | 10 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0004 | 0/0 | 777 | 17 | 7 | 8 | 0 | 1 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0005 | 0/0 | 777 | 16 | 8 | 1 | 6 | 0 | 1 | 4 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0006 | 0/0 | 777 | 8 | 0 | 0 | 8 | 0 | 0 | 8 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0007 | 0/0 | 777 | 8 | 0 | 7 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0008 | 0/0 | 777 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0009 | 0/0 | 777 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0010 | 0/0 | 777 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0011 | 0/0 | 777 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0012 | 0/0 | 777 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0013 | 0/0 | 777 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0014 | 0/0 | 770 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0015 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0016 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0017 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0018 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0019 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0020 | 0/0 | 777 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0021 | 0/0 | 770 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0022 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0023 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2334 | 88 | 9 | 20 | 43 | 4 | 12 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0002 | 0/0 | 2334 | 69 | 11 | 11 | 35 | 2 | 10 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0003 | 0/1 | 2334 | 63 | 1 | 8 | 46 | 0 | 7 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0004 | 1/0 | 2334 | 29 | 24 | 2 | 0 | 0 | 2 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0005 | 0/0 | 2313 | 23 | 1 | 4 | 13 | 0 | 5 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0006 | 0/0 | 2334 | 16 | 8 | 1 | 6 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0007 | 0/0 | 2334 | 12 | 6 | 5 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0008 | 0/0 | 2334 | 8 | 0 | 0 | 8 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0009 | 0/0 | 2334 | 6 | 5 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0010 | 0/0 | 2334 | 5 | 1 | 3 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0011 | 0/0 | 2334 | 5 | 5 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0012 | 0/0 | 2334 | 5 | 5 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0013 | 0/0 | 2334 | 4 | 4 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0014 | 0/0 | 2334 | 4 | 3 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0015 | 0/0 | 2334 | 4 | 0 | 3 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0016 | 0/0 | 2313 | 2 | 0 | 0 | 1 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0017 | 0/0 | 2334 | 2 | 0 | 2 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0018 | 0/0 | 2334 | 2 | 0 | 2 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0019 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0020 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0021 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0022 | 0/0 | 2334 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0023 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0024 | 0/0 | 2313 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0025 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0026 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0027 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0028 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0029 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0030 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0031 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0032 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| c0033 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3147 | 70 | 9 | 14 | 34 | 0 | 12 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0002 | 0/0 | 3146 | 47 | 1 | 10 | 28 | 2 | 6 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0003 | 0/0 | 3141 | 37 | 1 | 4 | 23 | 2 | 7 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0004 | 0/0 | 3146 | 19 | 9 | 1 | 7 | 1 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0005 | 0/0 | 3145 | 17 | 0 | 2 | 15 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0006 | 0/0 | 3145 | 17 | 0 | 4 | 10 | 0 | 3 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0007 | 0/0 | 3141 | 13 | 0 | 2 | 10 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0008 | 0/0 | 3148 | 11 | 2 | 7 | 0 | 1 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0009 | 0/0 | 3147 | 10 | 10 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0010 | 0/0 | 3147 | 7 | 0 | 5 | 1 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0011 | 0/0 | 3148 | 6 | 1 | 0 | 5 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0012 | 0/0 | 3145 | 5 | 5 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0013 | 0/0 | 3145 | 5 | 4 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0014 | 0/0 | 3149 | 4 | 4 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0015 | 0/0 | 3145 | 4 | 3 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0016 | 0/0 | 3145 | 4 | 0 | 3 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0017 | 0/0 | 3148 | 4 | 3 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0018 | 0/0 | 3147 | 4 | 4 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0019 | 0/0 | 3142 | 4 | 0 | 3 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0020 | 0/0 | 3083 | 3 | 3 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0021 | 0/0 | 3146 | 3 | 3 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0022 | 0/0 | 3141 | 3 | 0 | 3 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0023 | 0/0 | 3147 | 3 | 3 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0024 | 0/0 | 3147 | 3 | 1 | 1 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0025 | 0/0 | 3145 | 3 | 3 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0026 | 0/0 | 3147 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0027 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0028 | 0/0 | 3145 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0029 | 0/0 | 3146 | 2 | 0 | 0 | 1 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0030 | 0/0 | 3147 | 2 | 0 | 2 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0031 | 0/0 | 3145 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0032 | 0/0 | 3084 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0033 | 0/0 | 3147 | 2 | 0 | 0 | 0 | 0 | 2 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0034 | 0/0 | 3147 | 2 | 1 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0035 | 0/0 | 3146 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0036 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0037 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0038 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0039 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0040 | 0/0 | 3146 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0041 | 0/0 | 3146 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0042 | 0/0 | 3146 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0043 | 0/0 | 3146 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0044 | 0/0 | 3142 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0045 | 0/0 | 3145 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0046 | 0/0 | 3084 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0047 | 0/0 | 3085 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0048 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0049 | 0/0 | 3146 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0050 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0051 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0052 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0053 | 0/0 | 3146 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0054 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0055 | 0/0 | 3148 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0056 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0057 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0058 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0059 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0060 | 0/0 | 3146 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0061 | 0/0 | 3142 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0062 | 0/0 | 3141 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0063 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0064 | 0/0 | 3145 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0065 | 1/0 | 3145 | 1 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0066 | 0/0 | 3145 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0067 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0068 | 0/0 | 3084 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0069 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0070 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| t0071 | 0/0 | 3144 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 2334 | 69 | 11 | 11 | 35 | 2 | 10 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0003 | 0/1 | 2334 | 63 | 1 | 8 | 46 | 0 | 7 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0004 | 1/0 | 2334 | 29 | 24 | 2 | 0 | 0 | 2 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0019 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0021 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0022 | 0/0 | 2334 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001 | 0/0 | 2334 | 88 | 9 | 20 | 43 | 4 | 12 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0033 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0003c0005 | 0/0 | 2313 | 23 | 1 | 4 | 13 | 0 | 5 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0004c0007 | 0/0 | 2334 | 12 | 6 | 5 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0004c0010 | 0/0 | 2334 | 5 | 1 | 3 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0005c0006 | 0/0 | 2334 | 16 | 8 | 1 | 6 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0006c0008 | 0/0 | 2334 | 8 | 0 | 0 | 8 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0007c0015 | 0/0 | 2334 | 4 | 0 | 3 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0007c0018 | 0/0 | 2334 | 2 | 0 | 2 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0007c0030 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0007c0032 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0008c0009 | 0/0 | 2334 | 6 | 5 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0009c0011 | 0/0 | 2334 | 5 | 5 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0010c0012 | 0/0 | 2334 | 5 | 5 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0011c0014 | 0/0 | 2334 | 4 | 3 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0012c0013 | 0/0 | 2334 | 4 | 4 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0013c0017 | 0/0 | 2334 | 2 | 0 | 2 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0014c0016 | 0/0 | 2313 | 2 | 0 | 0 | 1 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0015c0028 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0016c0023 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0017c0027 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0018c0020 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0019c0026 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0020c0025 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0021c0024 | 0/0 | 2313 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0022c0029 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0023c0031 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0003 | 0/0 | 5474 | 36 | 1 | 4 | 23 | 1 | 7 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0002t0004 | 0/0 | 5479 | 17 | 7 | 1 | 7 | 1 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0002t0007 | 0/0 | 5474 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0002t0013 | 0/0 | 5478 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0002t0019 | 0/0 | 5475 | 4 | 0 | 3 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0002t0022 | 0/0 | 5474 | 2 | 0 | 2 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0002t0024 | 0/0 | 5480 | 2 | 0 | 1 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0002t0059 | 0/0 | 5474 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0002t0060 | 0/0 | 5479 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0002t0061 | 0/0 | 5475 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0002t0062 | 0/0 | 5474 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0002t0063 | 0/0 | 5480 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0003t0001 | 0/1 | 5480 | 1 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0003t0002 | 0/0 | 5479 | 34 | 1 | 4 | 25 | 0 | 4 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0003t0005 | 0/0 | 5478 | 8 | 0 | 1 | 7 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0003t0007 | 0/0 | 5474 | 7 | 0 | 0 | 7 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0003t0010 | 0/0 | 5480 | 5 | 0 | 3 | 1 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0003t0028 | 0/0 | 5478 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0003t0031 | 0/0 | 5478 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0003t0040 | 0/0 | 5479 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0003t0042 | 0/0 | 5479 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0003t0043 | 0/0 | 5479 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0003t0053 | 0/0 | 5479 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0004t0008 | 0/0 | 5481 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0004t0009 | 0/0 | 5480 | 8 | 8 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0004t0011 | 0/0 | 5481 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0004t0014 | 0/0 | 5482 | 4 | 4 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0004t0017 | 0/0 | 5481 | 4 | 3 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0004t0018 | 0/0 | 5480 | 4 | 4 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0004t0027 | 0/0 | 5483 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0004t0033 | 0/0 | 5480 | 2 | 0 | 0 | 0 | 0 | 2 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0004t0051 | 0/0 | 5481 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0004t0057 | 0/0 | 5481 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0004t0065 | 1/0 | 5478 | 1 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0019t0056 | 0/0 | 5480 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0021t0022 | 0/0 | 5474 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0001c0022t0003 | 0/0 | 5474 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001t0001 | 0/0 | 5480 | 61 | 7 | 14 | 29 | 0 | 11 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001t0002 | 0/0 | 5479 | 5 | 0 | 1 | 1 | 2 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001t0005 | 0/0 | 5478 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001t0007 | 0/0 | 5474 | 5 | 0 | 2 | 2 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001t0009 | 0/0 | 5480 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001t0011 | 0/0 | 5481 | 4 | 0 | 0 | 4 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001t0016 | 0/0 | 5478 | 4 | 0 | 3 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001t0026 | 0/0 | 5480 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001t0037 | 0/0 | 5480 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001t0038 | 0/0 | 5480 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001t0039 | 0/0 | 5480 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001t0045 | 0/0 | 5478 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0001t0048 | 0/0 | 5480 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0002c0033t0001 | 0/0 | 5480 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0003c0005t0005 | 0/0 | 5457 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0003c0005t0006 | 0/0 | 5457 | 16 | 0 | 3 | 10 | 0 | 3 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0003c0005t0034 | 0/0 | 5459 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0003c0005t0035 | 0/0 | 5458 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0003c0005t0041 | 0/0 | 5458 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0003c0005t0055 | 0/0 | 5460 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0003c0005t0064 | 0/0 | 5457 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0004c0007t0008 | 0/0 | 5481 | 5 | 1 | 3 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0004c0007t0013 | 0/0 | 5478 | 3 | 2 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0004c0007t0030 | 0/0 | 5480 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0004c0007t0036 | 0/0 | 5481 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0004c0007t0058 | 0/0 | 5481 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0004c0007t0068 | 0/0 | 5417 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0004c0010t0008 | 0/0 | 5481 | 4 | 1 | 2 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0004c0010t0030 | 0/0 | 5480 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0005c0006t0001 | 0/0 | 5480 | 6 | 1 | 0 | 4 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0005c0006t0009 | 0/0 | 5480 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0005c0006t0011 | 0/0 | 5481 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0005c0006t0020 | 0/0 | 5416 | 3 | 3 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0005c0006t0034 | 0/0 | 5480 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0005c0006t0046 | 0/0 | 5417 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0005c0006t0050 | 0/0 | 5480 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0005c0006t0054 | 0/0 | 5480 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0005c0006t0066 | 0/0 | 5478 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0006c0008t0001 | 0/0 | 5480 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0006c0008t0005 | 0/0 | 5478 | 6 | 0 | 0 | 6 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0006c0008t0029 | 0/0 | 5479 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0007c0015t0002 | 0/0 | 5479 | 4 | 0 | 3 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0007c0018t0010 | 0/0 | 5480 | 2 | 0 | 2 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0007c0030t0044 | 0/0 | 5475 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0007c0032t0002 | 0/0 | 5479 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0008c0009t0021 | 0/0 | 5479 | 3 | 3 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0008c0009t0025 | 0/0 | 5478 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0008c0009t0049 | 0/0 | 5479 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0009c0011t0032 | 0/0 | 5417 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0009c0011t0047 | 0/0 | 5418 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0009c0011t0069 | 0/0 | 5480 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0009c0011t0070 | 0/0 | 5481 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0010c0012t0012 | 0/0 | 5478 | 5 | 5 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0011c0014t0015 | 0/0 | 5478 | 4 | 3 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0012c0013t0023 | 0/0 | 5480 | 3 | 3 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0012c0013t0052 | 0/0 | 5481 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0013c0017t0002 | 0/0 | 5479 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0013c0017t0008 | 0/0 | 5481 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0014c0016t0005 | 0/0 | 5457 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0014c0016t0029 | 0/0 | 5458 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0015c0028t0067 | 0/0 | 5480 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0016c0023t0004 | 0/0 | 5479 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0017c0027t0002 | 0/0 | 5479 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0018c0020t0024 | 0/0 | 5480 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0019c0026t0025 | 0/0 | 5478 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0020c0025t0071 | 0/0 | 5477 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0021c0024t0006 | 0/0 | 5457 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0022c0029t0004 | 0/0 | 5479 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| a0023c0031t0002 | 0/0 | 5479 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | copy fasta | chr2 | 214720646 | 214814683 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0013g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0013g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0019g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0019g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0019g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0019g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0022g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0022g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0024g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0024g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0059g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0060g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0061g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0062g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0002t0063g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0001g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0007g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0007g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0010g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0010g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0010g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0010g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0010g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0028g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0028g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0031g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0031g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0040g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0042g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0043g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0003t0053g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0008g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0009g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0009g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0009g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0011g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0014g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0014g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0017g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0017g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0017g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0017g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0018g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0018g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0018g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0018g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0027g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0027g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0033g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0033g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0051g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0057g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0004t0065g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0019t0056g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0021t0022g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0001c0022t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0007g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0007g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0011g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0011g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0011g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0011g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0016g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0016g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0016g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0026g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0026g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0037g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0038g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0039g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0045g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0001t0048g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0002c0033t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0006g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0034g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0035g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0035g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0041g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0055g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0003c0005t0064g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0007t0008g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0007t0008g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0007t0008g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0007t0008g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0007t0008g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0007t0013g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0007t0013g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0007t0013g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0007t0030g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0007t0036g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0007t0058g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0007t0068g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0010t0008g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0010t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0010t0008g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0004c0010t0030g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0011g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0020g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0020g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0020g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0034g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0046g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0050g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0054g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0005c0006t0066g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0006c0008t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0006c0008t0005g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0006c0008t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0006c0008t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0006c0008t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0006c0008t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0006c0008t0029g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0007c0015t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0007c0015t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0007c0015t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0007c0015t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0007c0018t0010g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0007c0018t0010g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0007c0030t0044g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0007c0032t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0008c0009t0021g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0008c0009t0021g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0008c0009t0025g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0008c0009t0025g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0008c0009t0049g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0009c0011t0032g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0009c0011t0032g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0009c0011t0047g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0009c0011t0069g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0009c0011t0070g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0010c0012t0012g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0010c0012t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0010c0012t0012g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0010c0012t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0011c0014t0015g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0011c0014t0015g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0011c0014t0015g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0012c0013t0023g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0012c0013t0023g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0012c0013t0023g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0012c0013t0052g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0013c0017t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0013c0017t0008g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0014c0016t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0014c0016t0029g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0015c0028t0067g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0016c0023t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0017c0027t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0018c0020t0024g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0019c0026t0025g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0020c0025t0071g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0021c0024t0006g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0022c0029t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| a0023c0031t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0039 | g0190 | EUR | GBR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00099 | hp2 | a0004 | c0010 | t0008 | g0106 | EUR | GBR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00280 | hp1 | a0002 | c0001 | t0007 | g0169 | EUR | FIN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0329 | EUR | FIN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00408 | hp1 | a0001 | c0002 | t0004 | g0305 | EAS | CHS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00408 | hp2 | a0002 | c0001 | t0011 | g0137 | EAS | CHS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0151 | EAS | CHS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00438 | hp2 | a0001 | c0003 | t0002 | g0045 | EAS | CHS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00609 | hp1 | a0002 | c0001 | t0001 | g0173 | EAS | CHS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00609 | hp2 | a0003 | c0005 | t0006 | g0251 | EAS | CHS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00621 | hp1 | a0005 | c0006 | t0001 | g0029 | EAS | CHS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00621 | hp2 | a0003 | c0005 | t0006 | g0258 | EAS | CHS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00639 | hp1 | a0002 | c0001 | t0002 | g0216 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0170 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0321 | EAS | CHS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00673 | hp2 | a0001 | c0003 | t0031 | g0086 | EAS | CHS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00733 | hp1 | a0001 | c0002 | t0019 | g0290 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00733 | hp2 | a0002 | c0001 | t0001 | g0196 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00735 | hp1 | a0007 | c0015 | t0002 | g0218 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00735 | hp2 | a0003 | c0005 | t0006 | g0242 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00741 | hp1 | a0002 | c0001 | t0007 | g0148 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG00741 | hp2 | a0001 | c0004 | t0008 | g0103 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01069 | hp1 | a0002 | c0001 | t0016 | g0011 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01069 | hp2 | a0004 | c0007 | t0030 | g0034 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01071 | hp1 | a0002 | c0001 | t0016 | g0011 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01071 | hp2 | a0005 | c0006 | t0066 | g0333 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01074 | hp1 | a0007 | c0015 | t0002 | g0220 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01074 | hp2 | a0011 | c0014 | t0015 | g0118 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0197 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01081 | hp2 | a0020 | c0025 | t0071 | g0338 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01106 | hp1 | a0002 | c0001 | t0001 | g0175 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01106 | hp2 | a0001 | c0002 | t0019 | g0302 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01109 | hp1 | a0001 | c0003 | t0010 | g0091 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01109 | hp2 | a0008 | c0009 | t0049 | g0222 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0314 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01167 | hp2 | a0002 | c0001 | t0001 | g0149 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01169 | hp1 | a0004 | c0010 | t0030 | g0104 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0313 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01175 | hp1 | a0004 | c0007 | t0008 | g0031 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01175 | hp2 | a0001 | c0002 | t0024 | g0270 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01192 | hp1 | a0002 | c0001 | t0001 | g0147 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01192 | hp2 | a0007 | c0030 | t0044 | g0153 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0293 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01243 | hp2 | a0002 | c0001 | t0016 | g0180 | AMR | PUR | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01255 | hp1 | a0001 | c0002 | t0022 | g0235 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01255 | hp2 | a0003 | c0005 | t0006 | g0016 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01256 | hp1 | a0004 | c0007 | t0013 | g0269 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01256 | hp2 | a0002 | c0001 | t0001 | g0133 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01257 | hp1 | a0001 | c0003 | t0002 | g0092 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01257 | hp2 | a0004 | c0010 | t0008 | g0003 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01258 | hp1 | a0004 | c0010 | t0008 | g0003 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01258 | hp2 | a0002 | c0001 | t0001 | g0134 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01346 | hp1 | a0001 | c0002 | t0019 | g0306 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01346 | hp2 | a0002 | c0001 | t0001 | g0165 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01358 | hp1 | a0002 | c0001 | t0001 | g0189 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01358 | hp2 | a0001 | c0002 | t0003 | g0311 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01361 | hp1 | a0013 | c0017 | t0008 | g0179 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01361 | hp2 | a0003 | c0005 | t0006 | g0016 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01433 | hp1 | a0002 | c0001 | t0007 | g0150 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0323 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01496 | hp1 | a0004 | c0007 | t0008 | g0037 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0102 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01516 | hp1 | a0001 | c0022 | t0003 | g0271 | EUR | IBS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01516 | hp2 | a0002 | c0001 | t0002 | g0014 | EUR | IBS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01517 | hp1 | a0002 | c0001 | t0002 | g0014 | EUR | IBS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01517 | hp2 | a0001 | c0002 | t0004 | g0297 | EUR | IBS | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01884 | hp1 | a0001 | c0004 | t0009 | g0109 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01884 | hp2 | a0005 | c0006 | t0020 | g0023 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01891 | hp1 | a0004 | c0010 | t0008 | g0105 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01891 | hp2 | a0002 | c0001 | t0001 | g0214 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01934 | hp1 | a0013 | c0017 | t0002 | g0141 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01934 | hp2 | a0002 | c0001 | t0001 | g0146 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01952 | hp1 | a0001 | c0021 | t0022 | g0236 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01952 | hp2 | a0002 | c0001 | t0001 | g0145 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0140 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01975 | hp2 | a0001 | c0003 | t0010 | g0098 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0188 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01978 | hp2 | a0001 | c0003 | t0002 | g0099 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01981 | hp1 | a0021 | c0024 | t0006 | g0247 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01981 | hp2 | a0007 | c0015 | t0002 | g0195 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02004 | hp1 | a0007 | c0018 | t0010 | g0187 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02004 | hp2 | a0001 | c0003 | t0005 | g0073 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0161 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02015 | hp2 | a0001 | c0003 | t0002 | g0088 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02040 | hp1 | a0001 | c0003 | t0002 | g0069 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02055 | hp1 | a0010 | c0012 | t0012 | g0215 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02055 | hp2 | a0005 | c0006 | t0020 | g0022 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02056 | hp1 | a0001 | c0003 | t0002 | g0058 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02056 | hp2 | a0002 | c0001 | t0001 | g0198 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0143 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0076 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0320 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02074 | hp2 | a0002 | c0001 | t0016 | g0131 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02080 | hp1 | a0002 | c0001 | t0007 | g0142 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0288 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0272 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0018 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02132 | hp1 | a0002 | c0001 | t0001 | g0156 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02132 | hp2 | a0001 | c0003 | t0007 | g0074 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02135 | hp1 | a0002 | c0001 | t0002 | g0182 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0159 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02155 | hp1 | a0001 | c0003 | t0002 | g0046 | EAS | CDX | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02155 | hp2 | a0003 | c0005 | t0006 | g0252 | EAS | CDX | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02165 | hp1 | a0001 | c0003 | t0002 | g0059 | EAS | CDX | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0287 | EAS | CDX | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02257 | hp1 | a0001 | c0002 | t0013 | g0276 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02257 | hp2 | a0001 | c0004 | t0017 | g0232 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02258 | hp1 | a0001 | c0003 | t0002 | g0114 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02258 | hp2 | a0002 | c0001 | t0001 | g0007 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02273 | hp1 | a0007 | c0032 | t0002 | g0194 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02273 | hp2 | a0001 | c0004 | t0017 | g0239 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0316 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02280 | hp2 | a0001 | c0004 | t0009 | g0113 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02293 | hp1 | a0004 | c0007 | t0008 | g0033 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02293 | hp2 | a0001 | c0003 | t0002 | g0097 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02300 | hp1 | a0001 | c0002 | t0022 | g0233 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02300 | hp2 | a0003 | c0005 | t0005 | g0101 | AMR | PEL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02451 | hp1 | a0003 | c0005 | t0041 | g0026 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02451 | hp2 | a0001 | c0002 | t0004 | g0296 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02523 | hp1 | a0002 | c0001 | t0001 | g0168 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02523 | hp2 | a0001 | c0002 | t0003 | g0312 | EAS | KHV | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02572 | hp1 | a0001 | c0004 | t0018 | g0277 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02572 | hp2 | a0012 | c0013 | t0052 | g0226 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02615 | hp1 | a0001 | c0004 | t0009 | g0125 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02615 | hp2 | a0018 | c0020 | t0024 | g0284 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02622 | hp1 | a0001 | c0004 | t0018 | g0281 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02622 | hp2 | a0001 | c0004 | t0009 | g0111 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02630 | hp1 | a0005 | c0006 | t0034 | g0262 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02630 | hp2 | a0008 | c0009 | t0025 | g0266 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02647 | hp1 | a0001 | c0004 | t0011 | g0121 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02647 | hp2 | a0002 | c0001 | t0009 | g0139 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02683 | hp1 | a0001 | c0002 | t0019 | g0309 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02683 | hp2 | a0002 | c0001 | t0001 | g0136 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02723 | hp1 | a0001 | c0004 | t0009 | g0112 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02723 | hp2 | a0004 | c0007 | t0068 | g0265 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0193 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02735 | hp2 | a0007 | c0015 | t0002 | g0219 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02738 | hp1 | a0001 | c0003 | t0002 | g0048 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02738 | hp2 | a0002 | c0001 | t0001 | g0128 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02809 | hp1 | a0010 | c0012 | t0012 | g0201 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02809 | hp2 | a0005 | c0006 | t0050 | g0224 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02818 | hp1 | a0001 | c0004 | t0009 | g0004 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02818 | hp2 | a0012 | c0013 | t0023 | g0227 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02886 | hp1 | a0001 | c0004 | t0018 | g0279 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02886 | hp2 | a0008 | c0009 | t0021 | g0015 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02895 | hp1 | a0005 | c0006 | t0020 | g0024 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02895 | hp2 | a0011 | c0014 | t0015 | g0005 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02896 | hp1 | a0010 | c0012 | t0012 | g0012 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02896 | hp2 | a0001 | c0002 | t0060 | g0292 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02897 | hp1 | a0010 | c0012 | t0012 | g0012 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02897 | hp2 | a0011 | c0014 | t0015 | g0005 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02922 | hp1 | a0001 | c0004 | t0057 | g0278 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02922 | hp2 | a0009 | c0011 | t0069 | g0336 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02965 | hp1 | a0009 | c0011 | t0032 | g0025 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02965 | hp2 | a0012 | c0013 | t0023 | g0225 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0285 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02970 | hp2 | a0002 | c0001 | t0001 | g0007 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03017 | hp1 | a0001 | c0003 | t0002 | g0061 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0298 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03041 | hp1 | a0005 | c0006 | t0046 | g0035 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03041 | hp2 | a0005 | c0006 | t0001 | g0120 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03098 | hp1 | a0012 | c0013 | t0023 | g0228 | AFR | MSL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03098 | hp2 | a0005 | c0006 | t0009 | g0117 | AFR | MSL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03130 | hp1 | a0001 | c0019 | t0056 | g0330 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03130 | hp2 | a0008 | c0009 | t0021 | g0223 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0017 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03139 | hp2 | a0002 | c0001 | t0001 | g0167 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03195 | hp1 | a0008 | c0009 | t0021 | g0015 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03195 | hp2 | a0009 | c0011 | t0032 | g0115 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03209 | hp1 | a0022 | c0029 | t0004 | g0295 | AFR | MSL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03209 | hp2 | a0010 | c0012 | t0012 | g0202 | AFR | MSL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03225 | hp1 | a0001 | c0004 | t0027 | g0123 | AFR | MSL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03225 | hp2 | a0001 | c0002 | t0013 | g0322 | AFR | MSL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03239 | hp1 | a0002 | c0001 | t0001 | g0008 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03239 | hp2 | a0001 | c0004 | t0033 | g0229 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03453 | hp1 | a0011 | c0014 | t0015 | g0119 | AFR | MSL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03453 | hp2 | a0002 | c0001 | t0038 | g0160 | AFR | MSL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0300 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03490 | hp2 | a0001 | c0004 | t0033 | g0237 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0299 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03491 | hp2 | a0002 | c0001 | t0002 | g0217 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03516 | hp1 | a0001 | c0002 | t0004 | g0289 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0282 | AFR | ESN | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03540 | hp1 | a0002 | c0001 | t0001 | g0163 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03540 | hp2 | a0002 | c0001 | t0001 | g0154 | AFR | GWD | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03579 | hp1 | a0001 | c0004 | t0027 | g0124 | AFR | MSL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03579 | hp2 | a0001 | c0004 | t0009 | g0110 | AFR | MSL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03688 | hp1 | a0001 | c0003 | t0002 | g0049 | SAS | STU | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03688 | hp2 | a0002 | c0001 | t0001 | g0212 | SAS | STU | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03704 | hp1 | a0001 | c0003 | t0040 | g0052 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0172 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03710 | hp1 | a0004 | c0007 | t0008 | g0039 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03710 | hp2 | a0002 | c0001 | t0001 | g0127 | SAS | PJL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0020 | SAS | BEB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03831 | hp2 | a0005 | c0006 | t0001 | g0036 | SAS | BEB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03834 | hp1 | a0002 | c0001 | t0001 | g0191 | SAS | BEB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0286 | SAS | BEB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03927 | hp1 | a0003 | c0005 | t0006 | g0274 | SAS | BEB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03927 | hp2 | a0001 | c0002 | t0004 | g0291 | SAS | BEB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03942 | hp1 | a0001 | c0003 | t0002 | g0068 | SAS | BEB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03942 | hp2 | a0014 | c0016 | t0029 | g0152 | SAS | BEB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG04115 | hp1 | a0001 | c0003 | t0010 | g0044 | SAS | STU | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG04115 | hp2 | a0001 | c0003 | t0053 | g0234 | SAS | STU | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG04184 | hp1 | a0003 | c0005 | t0006 | g0273 | SAS | BEB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG04184 | hp2 | a0002 | c0001 | t0001 | g0213 | SAS | BEB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG04199 | hp1 | a0003 | c0005 | t0055 | g0245 | SAS | STU | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG04199 | hp2 | a0001 | c0002 | t0062 | g0328 | SAS | STU | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0260 | SAS | STU | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG04204 | hp2 | a0003 | c0005 | t0064 | g0246 | SAS | STU | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0008 | SAS | STU | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG04228 | hp2 | a0003 | c0005 | t0006 | g0256 | SAS | STU | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18522 | hp1 | a0001 | c0004 | t0051 | g0230 | AFR | YRI | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18522 | hp2 | a0009 | c0011 | t0047 | g0116 | AFR | YRI | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18747 | hp1 | a0001 | c0003 | t0031 | g0072 | EAS | CHB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18747 | hp2 | a0005 | c0006 | t0001 | g0093 | EAS | CHB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18906 | hp1 | a0019 | c0026 | t0025 | g0331 | AFR | YRI | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18906 | hp2 | a0001 | c0004 | t0017 | g0238 | AFR | YRI | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0162 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18939 | hp2 | a0001 | c0002 | t0003 | g0275 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18943 | hp1 | a0003 | c0005 | t0006 | g0249 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18943 | hp2 | a0001 | c0003 | t0002 | g0028 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18944 | hp2 | a0001 | c0002 | t0004 | g0019 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18945 | hp1 | a0002 | c0001 | t0045 | g0130 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18945 | hp2 | a0001 | c0002 | t0004 | g0325 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18946 | hp1 | a0001 | c0002 | t0003 | g0310 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18946 | hp2 | a0001 | c0003 | t0005 | g0066 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18949 | hp1 | a0002 | c0001 | t0001 | g0164 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18949 | hp2 | a0001 | c0003 | t0002 | g0053 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18951 | hp1 | a0003 | c0005 | t0035 | g0257 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18951 | hp2 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18953 | hp1 | a0001 | c0003 | t0010 | g0047 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18953 | hp2 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18956 | hp1 | a0005 | c0006 | t0054 | g0240 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18956 | hp2 | a0001 | c0003 | t0043 | g0063 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18957 | hp1 | a0001 | c0003 | t0002 | g0077 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18957 | hp2 | a0003 | c0005 | t0006 | g0243 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18960 | hp1 | a0003 | c0005 | t0006 | g0248 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0177 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18962 | hp1 | a0005 | c0006 | t0001 | g0084 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0307 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0192 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18964 | hp2 | a0001 | c0003 | t0002 | g0094 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18966 | hp1 | a0001 | c0002 | t0007 | g0056 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0303 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18968 | hp2 | a0023 | c0031 | t0002 | g0155 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18969 | hp1 | a0001 | c0002 | t0004 | g0019 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18969 | hp2 | a0001 | c0003 | t0002 | g0075 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18970 | hp1 | a0014 | c0016 | t0005 | g0200 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18970 | hp2 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18971 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18971 | hp2 | a0002 | c0001 | t0005 | g0207 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18972 | hp1 | a0001 | c0002 | t0003 | g0334 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18972 | hp2 | a0003 | c0005 | t0035 | g0259 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18973 | hp1 | a0006 | c0008 | t0005 | g0203 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18973 | hp2 | a0001 | c0002 | t0004 | g0327 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18977 | hp1 | a0001 | c0002 | t0003 | g0018 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18977 | hp2 | a0001 | c0003 | t0007 | g0050 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18978 | hp1 | a0001 | c0003 | t0005 | g0096 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18978 | hp2 | a0001 | c0003 | t0007 | g0081 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18981 | hp1 | a0001 | c0003 | t0002 | g0071 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18981 | hp2 | a0003 | c0005 | t0006 | g0253 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18983 | hp2 | a0002 | c0001 | t0037 | g0178 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18984 | hp1 | a0001 | c0003 | t0002 | g0070 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18984 | hp2 | a0002 | c0001 | t0001 | g0166 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18986 | hp1 | a0001 | c0003 | t0002 | g0027 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18986 | hp2 | a0003 | c0005 | t0006 | g0244 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18987 | hp1 | a0002 | c0001 | t0011 | g0211 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18987 | hp2 | a0001 | c0003 | t0042 | g0051 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18988 | hp1 | a0002 | c0001 | t0007 | g0199 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18988 | hp2 | a0001 | c0003 | t0007 | g0055 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18989 | hp1 | a0001 | c0003 | t0007 | g0082 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18989 | hp2 | a0002 | c0001 | t0001 | g0184 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18990 | hp1 | a0001 | c0002 | t0003 | g0332 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18991 | hp1 | a0001 | c0003 | t0002 | g0087 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18991 | hp2 | a0002 | c0001 | t0026 | g0158 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18992 | hp1 | a0006 | c0008 | t0005 | g0205 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18992 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18993 | hp1 | a0001 | c0003 | t0005 | g0043 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18993 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18994 | hp1 | a0002 | c0001 | t0011 | g0183 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18994 | hp2 | a0001 | c0003 | t0002 | g0090 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18995 | hp1 | a0002 | c0001 | t0011 | g0171 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18995 | hp2 | a0001 | c0002 | t0059 | g0318 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18997 | hp1 | a0001 | c0003 | t0005 | g0108 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18997 | hp2 | a0005 | c0006 | t0011 | g0083 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0079 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18998 | hp2 | a0001 | c0003 | t0002 | g0054 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19000 | hp1 | a0006 | c0008 | t0029 | g0210 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0315 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19001 | hp1 | a0001 | c0002 | t0061 | g0304 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19001 | hp2 | a0002 | c0001 | t0001 | g0208 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19004 | hp1 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19004 | hp2 | a0003 | c0005 | t0006 | g0254 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0317 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19009 | hp2 | a0002 | c0001 | t0026 | g0157 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0283 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19010 | hp2 | a0001 | c0003 | t0005 | g0065 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19011 | hp1 | a0006 | c0008 | t0005 | g0209 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19011 | hp2 | a0001 | c0002 | t0024 | g0324 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19012 | hp1 | a0001 | c0003 | t0005 | g0064 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19012 | hp2 | a0002 | c0001 | t0048 | g0221 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19030 | hp1 | a0001 | c0004 | t0017 | g0231 | AFR | LWK | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19030 | hp2 | a0004 | c0007 | t0036 | g0038 | AFR | LWK | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19043 | hp1 | a0002 | c0033 | t0001 | g0181 | AFR | LWK | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19043 | hp2 | a0004 | c0007 | t0008 | g0126 | AFR | LWK | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19055 | hp1 | a0001 | c0003 | t0002 | g0040 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19055 | hp2 | a0002 | c0001 | t0001 | g0129 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0301 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19060 | hp2 | a0002 | c0001 | t0001 | g0185 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19062 | hp1 | a0001 | c0003 | t0002 | g0095 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19062 | hp2 | a0003 | c0005 | t0006 | g0250 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19063 | hp1 | a0001 | c0003 | t0028 | g0060 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19063 | hp2 | a0002 | c0001 | t0001 | g0174 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19066 | hp2 | a0017 | c0027 | t0002 | g0085 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19070 | hp1 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19070 | hp2 | a0006 | c0008 | t0005 | g0204 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19072 | hp1 | a0002 | c0001 | t0001 | g0176 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19072 | hp2 | a0001 | c0003 | t0028 | g0062 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19074 | hp1 | a0006 | c0008 | t0001 | g0206 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19074 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19076 | hp1 | a0001 | c0003 | t0002 | g0078 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19076 | hp2 | a0003 | c0005 | t0034 | g0255 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19079 | hp1 | a0002 | c0001 | t0001 | g0132 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0335 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19081 | hp1 | a0005 | c0006 | t0001 | g0030 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19081 | hp2 | a0001 | c0003 | t0002 | g0107 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19082 | hp1 | a0001 | c0002 | t0063 | g0326 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19082 | hp2 | a0006 | c0008 | t0005 | g0013 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19088 | hp1 | a0001 | c0003 | t0002 | g0067 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19088 | hp2 | a0006 | c0008 | t0005 | g0013 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0308 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19090 | hp2 | a0001 | c0003 | t0005 | g0080 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0017 | AFR | YRI | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA19240 | hp2 | a0001 | c0004 | t0018 | g0280 | AFR | YRI | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA20129 | hp1 | a0002 | c0001 | t0001 | g0138 | AFR | ASW | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA20129 | hp2 | a0001 | c0004 | t0014 | g0006 | AFR | ASW | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0135 | SAS | GIH | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0020 | SAS | GIH | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01123 | hp1 | a0001 | c0003 | t0010 | g0100 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG01123 | hp2 | a0007 | c0018 | t0010 | g0186 | AMR | CLM | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02109 | hp1 | a0001 | c0004 | t0009 | g0004 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02109 | hp2 | a0015 | c0028 | t0067 | g0241 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02486 | hp1 | a0008 | c0009 | t0025 | g0267 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02486 | hp2 | a0009 | c0011 | t0070 | g0337 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02559 | hp1 | a0004 | c0007 | t0058 | g0263 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG02559 | hp2 | a0001 | c0004 | t0014 | g0122 | AFR | ACB | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03471 | hp1 | a0001 | c0004 | t0014 | g0032 | AFR | MSL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| HG03471 | hp2 | a0016 | c0023 | t0004 | g0294 | AFR | MSL | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18955 | hp1 | a0001 | c0003 | t0007 | g0042 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA18955 | hp2 | a0001 | c0003 | t0007 | g0089 | EAS | JPT | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA20300 | hp1 | a0001 | c0004 | t0014 | g0006 | AFR | USA | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA20300 | hp2 | a0004 | c0007 | t0013 | g0264 | AFR | USA | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0319 | AFR | LWK | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| NA21309 | hp2 | a0004 | c0007 | t0013 | g0268 | AFR | LWK | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0041 | REF | REF | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0065 | g0261 | REF | REF | BARD1_chr2_214720646_214814683 | BARD1 | chr2 | 214720646 | 214814683 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:214728798
|
T | C | 1 | a0011 | 4 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
missense_variant | MODERATE | c.2212A>G | p.Ile738Val | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2326/5478 | 2212/2334 | 738/777 | chr2 | 214728798 | ||
| chr2:214728873
|
C | T | 1 | a0018 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.2137G>A | p.Val713Met | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2251/5478 | 2137/2334 | 713/777 | chr2 | 214728873 | ||
| chr2:214730440
|
G | A | 2 | a0017a0023 | 2 | NA18968.hp2 NA19066.hp2 |
missense_variant | MODERATE | c.1972C>T | p.Arg658Cys | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/11 | 2086/5478 | 1972/2334 | 658/777 | chr2 | 214730440 | ||
| chr2:214730479
|
A | G | 3 | a0008a0010a0019 | 12 | HG01109.hp2 HG02055.hp1 HG02486.hp1 others(9): Show |
missense_variant | MODERATE | c.1933T>C | p.Cys645Arg | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/11 | 2047/5478 | 1933/2334 | 645/777 | chr2 | 214730479 | ||
| chr2:214745767
|
C | A | 1 | a0021 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.1765G>T | p.Ala589Ser | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 8/11 | 1879/5478 | 1765/2334 | 589/777 | chr2 | 214745767 | ||
| chr2:214752454
|
C | G | 1 | a0020 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.1670G>C | p.Cys557Ser | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/11 | 1784/5478 | 1670/2334 | 557/777 | chr2 | 214752454 | ||
| chr2:214767531
|
C | T | 9 | a0002a0005a0006others(6): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
missense_variant | MODERATE | c.1519G>A | p.Val507Met | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/11 | 1633/5478 | 1519/2334 | 507/777 | chr2 | 214767531 | ||
| chr2:214780634
|
T | A | 1 | a0016 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1240A>T | p.Met414Leu | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/11 | 1354/5478 | 1240/2334 | 414/777 | chr2 | 214780634 | ||
| chr2:214780740
|
C | G | 12 | a0002a0004a0005others(9): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
missense_variant | MODERATE | c.1134G>C | p.Arg378Ser | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/11 | 1248/5478 | 1134/2334 | 378/777 | chr2 | 214780740 | ||
| chr2:214780778
|
GTGGTGAA others(14): Show |
G | 3 | a0003a0014a0021 | 26 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(23): Show |
conservative_inframe_deletion | MODERATE | c.1075_1095delTTGCCT others(15): Show |
p.Leu359_Pro365del | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/11 | 1209/5478 | 1075/2334 | 359/777 | chr2 | 214780778 | ||
| chr2:214780807
|
T | A | 1 | a0015 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1067A>T | p.Asn356Ile | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/11 | 1181/5478 | 1067/2334 | 356/777 | chr2 | 214780807 | ||
| chr2:214780880
|
T | G | 1 | a0022 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.994A>C | p.Ile332Leu | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/11 | 1108/5478 | 994/2334 | 332/777 | chr2 | 214780880 | ||
| chr2:214781152
|
G | C | 1 | a0006 | 8 | NA18973.hp1 NA18992.hp1 NA19000.hp1 others(5): Show |
missense_variant | MODERATE | c.722C>G | p.Ser241Cys | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/11 | 836/5478 | 722/2334 | 241/777 | chr2 | 214781152 | ||
| chr2:214781254
|
T | C | 1 | a0012 | 4 | HG02572.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
missense_variant | MODERATE | c.620A>G | p.Lys207Arg | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/11 | 734/5478 | 620/2334 | 207/777 | chr2 | 214781254 | ||
| chr2:214809500
|
G | A | 7 | a0002a0006a0007others(4): Show | 115 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
missense_variant | MODERATE | c.70C>T | p.Pro24Ser | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/11 | 184/5478 | 70/2334 | 24/777 | chr2 | 214809500 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:214728979
|
G | A | 1 | a0001c0021 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.2031C>T | p.Phe677Phe | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2145/5478 | 2031/2334 | 677/777 | chr2 | 214728979 | ||
| chr2:214730435
|
T | C | 1 | a0001c0022 | 1 | HG01516.hp1 | synonymous_variant | LOW | c.1977A>G | p.Arg659Arg | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/11 | 2091/5478 | 1977/2334 | 659/777 | chr2 | 214730435 | ||
| chr2:214767532
|
A | G | 23 | a0001c0002a0001c0003a0001c0021others(20): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
synonymous_variant | LOW | c.1518T>C | p.His506His | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/11 | 1632/5478 | 1518/2334 | 506/777 | chr2 | 214767532 | ||
| chr2:214780679
|
A | G | 1 | a0007c0032 | 1 | HG02273.hp1 | synonymous_variant | LOW | c.1195T>C | p.Leu399Leu | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/11 | 1309/5478 | 1195/2334 | 399/777 | chr2 | 214780679 | ||
| chr2:214780821
|
C | G | 7 | a0001c0002a0001c0021a0001c0022others(4): Show | 75 | HG00280.hp2 HG00408.hp1 HG00673.hp1 others(72): Show |
synonymous_variant | LOW | c.1053G>C | p.Thr351Thr | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/11 | 1167/5478 | 1053/2334 | 351/777 | chr2 | 214780821 | ||
| chr2:214781265
|
T | G | 2 | a0002c0033a0011c0014 | 5 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
synonymous_variant | LOW | c.609A>C | p.Gly203Gly | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/11 | 723/5478 | 609/2334 | 203/777 | chr2 | 214781265 | ||
| chr2:214792313
|
A | G | 1 | a0001c0019 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.348T>C | p.His116His | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/11 | 462/5478 | 348/2334 | 116/777 | chr2 | 214792313 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:214725686
|
G | A | 104 | a0001c0002t0003a0001c0002t0004a0001c0002t0007others(101): Show | 357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
3_prime_UTR_variant | MODIFIER | c.*2990C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2990 | chr2 | 214725686 | |||||
| chr2:214725704
|
G | C | 1 | a0008c0009t0049 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2972C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2972 | chr2 | 214725704 | |||||
| chr2:214725781
|
TAAGAC | T | 12 | a0001c0002t0003a0001c0002t0007a0001c0002t0019others(9): Show | 61 | HG00280.hp1 HG00280.hp2 HG00673.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2890_*2894delGTCT others(1): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2890 | chr2 | 214725781 | |||||
| chr2:214725858
|
C | T | 84 | a0001c0002t0003a0001c0002t0004a0001c0002t0007others(81): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*2818G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2818 | chr2 | 214725858 | |||||
| chr2:214725885
|
G | C | 36 | a0001c0002t0003a0001c0002t0004a0001c0002t0007others(33): Show | 150 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*2791C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2791 | chr2 | 214725885 | |||||
| chr2:214725913
|
A | G | 5 | a0004c0007t0068a0005c0006t0020a0005c0006t0046others(2): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2763T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2763 | chr2 | 214725913 | |||||
| chr2:214726037
|
C | CA | 34 | a0001c0002t0013a0001c0002t0061a0001c0003t0005others(31): Show | 82 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2638dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2638 | chr2 | 214726037 | |||||
| chr2:214726046
|
A | AG | 1 | a0005c0006t0020 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2629_*2630insC | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2629 | chr2 | 214726046 | |||||
| chr2:214726065
|
T | A | 19 | a0001c0003t0001a0001c0004t0011a0002c0001t0001others(16): Show | 91 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2611A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2611 | chr2 | 214726065 | |||||
| chr2:214726190
|
C | A | 1 | a0002c0001t0045 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2486G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2486 | chr2 | 214726190 | |||||
| chr2:214726244
|
T | C | 7 | a0001c0002t0013a0004c0007t0013a0004c0007t0068others(4): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2432A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2432 | chr2 | 214726244 | |||||
| chr2:214726447
|
A | T | 1 | a0001c0003t0042 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2229T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2229 | chr2 | 214726447 | |||||
| chr2:214726451
|
G | A | 1 | a0001c0003t0043 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2225C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2225 | chr2 | 214726451 | |||||
| chr2:214726487
|
T | C | 1 | a0012c0013t0052 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2189A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2189 | chr2 | 214726487 | |||||
| chr2:214726549
|
A | G | 1 | a0002c0001t0037 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2127T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2127 | chr2 | 214726549 | |||||
| chr2:214726597
|
C | T | 1 | a0003c0005t0064 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2079G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2079 | chr2 | 214726597 | |||||
| chr2:214726601
|
A | G | 1 | a0002c0001t0026 | 2 | NA18991.hp2 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2075T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 2075 | chr2 | 214726601 | |||||
| chr2:214726706
|
T | TA | 2 | a0001c0004t0014a0001c0004t0027 | 6 | HG02559.hp2 HG03225.hp1 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1969dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 1969 | chr2 | 214726706 | |||||
| chr2:214726718
|
T | C | 5 | a0004c0007t0068a0005c0006t0020a0005c0006t0046others(2): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1958A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 1958 | chr2 | 214726718 | |||||
| chr2:214726770
|
T | C | 1 | a0002c0001t0038 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1906A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 1906 | chr2 | 214726770 | |||||
| chr2:214726966
|
AAAGTGAC others(54): Show |
A | 5 | a0004c0007t0068a0005c0006t0020a0005c0006t0046others(2): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1649_*1709delATTT others(57): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 1649 | chr2 | 214726966 | |||||
| chr2:214727028
|
T | C | 5 | a0004c0007t0068a0005c0006t0020a0005c0006t0046others(2): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1648A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 1648 | chr2 | 214727028 | |||||
| chr2:214727051
|
C | T | 1 | a0005c0006t0046 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1625G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 1625 | chr2 | 214727051 | |||||
| chr2:214727063
|
T | C | 1 | a0001c0002t0062 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1613A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 1613 | chr2 | 214727063 | |||||
| chr2:214727269
|
C | T | 1 | a0003c0005t0041 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1407G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 1407 | chr2 | 214727269 | |||||
| chr2:214727436
|
T | G | 1 | a0002c0001t0039 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1240A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 1240 | chr2 | 214727436 | |||||
| chr2:214727566
|
C | G | 105 | a0001c0002t0003a0001c0002t0004a0001c0002t0007others(102): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*1110G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 1110 | chr2 | 214727566 | |||||
| chr2:214727582
|
G | A | 19 | a0001c0003t0001a0001c0004t0011a0002c0001t0001others(16): Show | 91 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1094C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 1094 | chr2 | 214727582 | |||||
| chr2:214727618
|
T | C | 7 | a0001c0002t0013a0004c0007t0013a0004c0007t0068others(4): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1058A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 1058 | chr2 | 214727618 | |||||
| chr2:214727857
|
G | A | 1 | a0020c0025t0071 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 819 | chr2 | 214727857 | |||||
| chr2:214728044
|
C | T | 1 | a0011c0014t0015 | 4 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*632G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 632 | chr2 | 214728044 | |||||
| chr2:214728048
|
A | C | 1 | a0001c0003t0040 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*628T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 628 | chr2 | 214728048 | |||||
| chr2:214728057
|
A | G | 1 | a0001c0002t0060 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*619T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 619 | chr2 | 214728057 | |||||
| chr2:214728065
|
G | A | 1 | a0004c0007t0036 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*611C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 611 | chr2 | 214728065 | |||||
| chr2:214728182
|
T | A | 31 | a0001c0003t0001a0001c0004t0009a0001c0004t0011others(28): Show | 113 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*494A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 494 | chr2 | 214728182 | |||||
| chr2:214728281
|
T | TA | 17 | a0001c0002t0019a0001c0002t0063a0001c0003t0010others(14): Show | 32 | HG00408.hp2 HG00733.hp1 HG01106.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*394dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 394 | chr2 | 214728281 | |||||
| chr2:214728281
|
TA | T | 5 | a0001c0003t0028a0003c0005t0035a0005c0006t0020others(2): Show | 9 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*394delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 394 | chr2 | 214728281 | |||||
| chr2:214728281
|
TAA | T | 15 | a0001c0003t0005a0002c0001t0005a0002c0001t0045others(12): Show | 49 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*393_*394delTT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 393 | chr2 | 214728281 | |||||
| chr2:214728360
|
A | G | 1 | a0001c0004t0018 | 4 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*316T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 316 | chr2 | 214728360 | |||||
| chr2:214728438
|
A | G | 1 | a0001c0002t0059 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*238T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 238 | chr2 | 214728438 | |||||
| chr2:214728509
|
T | C | 68 | a0001c0002t0013a0001c0003t0001a0001c0003t0005others(65): Show | 207 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*167A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 167 | chr2 | 214728509 | |||||
| chr2:214728537
|
C | CT | 49 | a0001c0002t0003a0001c0002t0004a0001c0002t0007others(46): Show | 191 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*138dupA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 138 | chr2 | 214728537 | |||||
| chr2:214728537
|
C | CTT | 44 | a0001c0002t0024a0001c0003t0001a0001c0004t0008others(41): Show | 145 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*137_*138dupAA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 138 | chr2 | 214728537 | |||||
| chr2:214728537
|
CT | C | 7 | a0001c0002t0013a0004c0007t0013a0004c0007t0068others(4): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*138delA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 11/11 | 138 | chr2 | 214728537 | |||||
| chr2:214809599
|
C | G | 72 | a0001c0002t0007a0001c0002t0022a0001c0003t0001others(69): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
5_prime_UTR_variant | MODIFIER | c.-30G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/11 | 30 | chr2 | 214809599 | |||||
| chr2:214809617
|
A | G | 74 | a0001c0002t0007a0001c0002t0022a0001c0003t0001others(71): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
5_prime_UTR_variant | MODIFIER | c.-48T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/11 | 48 | chr2 | 214809617 | |||||
| chr2:214809647
|
C | T | 61 | a0001c0002t0007a0001c0003t0001a0001c0003t0002others(58): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
5_prime_UTR_variant | MODIFIER | c.-78G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/11 | 78 | chr2 | 214809647 | |||||
| chr2:214809652
|
G | A | 3 | a0009c0011t0069a0009c0011t0070a0020c0025t0071 | 3 | HG01081.hp2 HG02486.hp2 HG02922.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-83C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/11 | chr2 | 214809652 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:214729019
|
G | A | 1 | a0002c0001t0001g0173 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2002-11C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729019 | ||||||
| chr2:214729122
|
T | C | 2 | a0005c0006t0009g0117a0012c0013t0052g0226 | 2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2002-114A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729122 | ||||||
| chr2:214729127
|
G | C | 192 | a0001c0002t0013g0276a0001c0002t0013g0322a0001c0003t0001g0041others(189): Show | 207 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.2002-119C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729127 | ||||||
| chr2:214729143
|
T | C | 1 | a0001c0003t0040g0052 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2002-135A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729143 | ||||||
| chr2:214729147
|
T | G | 192 | a0001c0002t0013g0276a0001c0002t0013g0322a0001c0003t0001g0041others(189): Show | 207 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.2002-139A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729147 | ||||||
| chr2:214729173
|
G | A | 1 | a0003c0005t0006g0244 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2002-165C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729173 | ||||||
| chr2:214729224
|
C | T | 1 | a0004c0007t0068g0265 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2002-216G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729224 | ||||||
| chr2:214729236
|
G | C | 1 | a0001c0004t0009g0112 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2002-228C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729236 | ||||||
| chr2:214729257
|
T | C | 13 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(10): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2002-249A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729257 | ||||||
| chr2:214729265
|
T | C | 1 | a0009c0011t0032g0115 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2002-257A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729265 | ||||||
| chr2:214729271
|
A | G | 3 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228 | 3 | HG02818.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2002-263T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729271 | ||||||
| chr2:214729413
|
G | A | 3 | a0008c0009t0021g0015a0008c0009t0021g0223a0008c0009t0049g0222 | 4 | HG01109.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2002-405C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729413 | ||||||
| chr2:214729452
|
G | C | 2 | a0001c0002t0003g0313a0001c0002t0003g0314 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2002-444C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729452 | ||||||
| chr2:214729545
|
C | T | 1 | a0001c0019t0056g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2002-537G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729545 | ||||||
| chr2:214729692
|
T | C | 1 | a0001c0002t0003g0310 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2002-684A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729692 | ||||||
| chr2:214729694
|
A | G | 3 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228 | 3 | HG02818.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2002-686T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729694 | ||||||
| chr2:214729744
|
G | A | 3 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228 | 3 | HG02818.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2001+667C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729744 | ||||||
| chr2:214729757
|
A | T | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2001+654T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729757 | ||||||
| chr2:214729898
|
C | G | 2 | a0008c0009t0025g0267a0019c0026t0025g0331 | 2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2001+513G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214729898 | ||||||
| chr2:214730001
|
A | C | 3 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228 | 3 | HG02818.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2001+410T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214730001 | ||||||
| chr2:214730187
|
G | A | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2001+224C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214730187 | ||||||
| chr2:214730275
|
C | G | 1 | a0001c0002t0003g0300 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2001+136G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214730275 | ||||||
| chr2:214730345
|
T | G | 10 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(7): Show | 10 | HG01256.hp1 HG02257.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2001+66A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 10/10 | chr2 | 214730345 | ||||||
| chr2:214730575
|
T | C | 4 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1904-67A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214730575 | ||||||
| chr2:214730604
|
C | T | 1 | a0001c0003t0010g0044 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1904-96G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214730604 | ||||||
| chr2:214730716
|
T | A | 141 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(138): Show | 149 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.1904-208A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214730716 | ||||||
| chr2:214730721
|
C | A | 100 | a0001c0003t0001g0041a0001c0004t0009g0004a0001c0004t0009g0109others(97): Show | 109 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1904-213G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214730721 | ||||||
| chr2:214730788
|
C | T | 83 | a0001c0003t0001g0041a0001c0004t0011g0121a0002c0001t0001g0001others(80): Show | 91 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1904-280G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214730788 | ||||||
| chr2:214730831
|
A | C | 8 | a0004c0007t0068g0265a0005c0006t0020g0022a0005c0006t0020g0023others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1904-323T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214730831 | ||||||
| chr2:214730921
|
C | T | 80 | a0001c0003t0001g0041a0002c0001t0001g0001a0002c0001t0001g0007others(77): Show | 88 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1904-413G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214730921 | ||||||
| chr2:214730967
|
T | C | 3 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228 | 3 | HG02818.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1904-459A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214730967 | ||||||
| chr2:214731036
|
C | T | 8 | a0004c0007t0068g0265a0005c0006t0020g0022a0005c0006t0020g0023others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1904-528G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214731036 | ||||||
| chr2:214731041
|
C | G | 337 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(334): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.1904-533G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214731041 | ||||||
| chr2:214731137
|
G | GA | 241 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(238): Show | 258 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.1904-630dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214731137 | ||||||
| chr2:214731148
|
G | A | 270 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(267): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1904-640C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214731148 | ||||||
| chr2:214731148
|
G | C | 1 | a0001c0003t0031g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1904-640C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214731148 | ||||||
| chr2:214731348
|
T | G | 13 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(10): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1904-840A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214731348 | ||||||
| chr2:214731425
|
C | T | 8 | a0002c0001t0005g0207a0002c0001t0045g0130a0006c0008t0005g0013others(5): Show | 9 | NA18945.hp1 NA18971.hp2 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.1904-917G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214731425 | ||||||
| chr2:214731590
|
G | A | 38 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(35): Show | 40 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1904-1082C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214731590 | ||||||
| chr2:214731745
|
T | C | 3 | a0004c0007t0013g0264a0004c0007t0013g0268a0004c0007t0013g0269 | 3 | HG01256.hp1 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1904-1237A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214731745 | ||||||
| chr2:214731761
|
G | A | 1 | a0004c0007t0058g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1904-1253C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214731761 | ||||||
| chr2:214731979
|
T | A | 2 | a0001c0002t0003g0312a0002c0001t0007g0199 | 2 | HG02523.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1904-1471A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214731979 | ||||||
| chr2:214732026
|
A | G | 1 | a0004c0007t0036g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1904-1518T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732026 | ||||||
| chr2:214732079
|
A | G | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1904-1571T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732079 | ||||||
| chr2:214732114
|
T | C | 2 | a0001c0004t0009g0109a0001c0004t0009g0110 | 2 | HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1904-1606A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732114 | ||||||
| chr2:214732385
|
T | C | 1 | a0003c0005t0006g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1904-1877A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732385 | ||||||
| chr2:214732423
|
T | C | 2 | a0001c0004t0009g0125a0001c0004t0051g0230 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1904-1915A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732423 | ||||||
| chr2:214732447
|
G | C | 272 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(269): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1904-1939C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732447 | ||||||
| chr2:214732449
|
G | A | 1 | a0001c0002t0024g0270 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1904-1941C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732449 | ||||||
| chr2:214732456
|
C | T | 1 | a0001c0002t0062g0328 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1904-1948G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732456 | ||||||
| chr2:214732521
|
A | G | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1904-2013T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732521 | ||||||
| chr2:214732595
|
T | C | 1 | a0019c0026t0025g0331 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1904-2087A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732595 | ||||||
| chr2:214732646
|
C | T | 244 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(241): Show | 261 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1904-2138G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732646 | ||||||
| chr2:214732681
|
C | A | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1904-2173G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732681 | ||||||
| chr2:214732690
|
T | C | 13 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(10): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1904-2182A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732690 | ||||||
| chr2:214732790
|
A | G | 13 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(10): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1904-2282T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732790 | ||||||
| chr2:214732873
|
C | G | 2 | a0002c0001t0001g0164a0002c0001t0001g0166 | 2 | NA18949.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1904-2365G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732873 | ||||||
| chr2:214732905
|
C | T | 15 | a0001c0002t0013g0276a0001c0002t0013g0322a0001c0004t0009g0109others(12): Show | 15 | HG01256.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1904-2397G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732905 | ||||||
| chr2:214732916
|
A | T | 48 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(45): Show | 52 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1904-2408T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732916 | ||||||
| chr2:214732975
|
T | G | 10 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(7): Show | 11 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1904-2467A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732975 | ||||||
| chr2:214732991
|
T | C | 101 | a0001c0003t0001g0041a0001c0004t0009g0004a0001c0004t0009g0109others(98): Show | 110 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1904-2483A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214732991 | ||||||
| chr2:214733010
|
A | G | 38 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(35): Show | 40 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1904-2502T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733010 | ||||||
| chr2:214733036
|
G | C | 1 | a0002c0001t0001g0214 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1904-2528C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733036 | ||||||
| chr2:214733185
|
C | T | 1 | a0001c0002t0003g0272 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1904-2677G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733185 | ||||||
| chr2:214733222
|
C | A | 38 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(35): Show | 40 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1904-2714G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733222 | ||||||
| chr2:214733274
|
T | C | 2 | a0009c0011t0069g0336a0009c0011t0070g0337 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1904-2766A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733274 | ||||||
| chr2:214733305
|
T | C | 5 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(2): Show | 5 | HG01256.hp1 HG02257.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1904-2797A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733305 | ||||||
| chr2:214733358
|
G | A | 319 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(316): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.1904-2850C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733358 | ||||||
| chr2:214733376
|
A | G | 1 | a0004c0007t0058g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1904-2868T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733376 | ||||||
| chr2:214733421
|
T | TAAAAC | 13 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(10): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1904-2914_1904-291 others(9): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733421 | ||||||
| chr2:214733465
|
G | A | 332 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(329): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1904-2957C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733465 | ||||||
| chr2:214733625
|
A | T | 13 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(10): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1904-3117T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733625 | ||||||
| chr2:214733818
|
G | A | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1904-3310C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733818 | ||||||
| chr2:214733861
|
C | T | 13 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(10): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1904-3353G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733861 | ||||||
| chr2:214733904
|
G | A | 1 | a0003c0005t0006g0256 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1904-3396C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214733904 | ||||||
| chr2:214734076
|
G | C | 2 | a0005c0006t0046g0035a0009c0011t0032g0115 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1904-3568C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214734076 | ||||||
| chr2:214734113
|
G | T | 1 | a0001c0003t0002g0049 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1904-3605C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214734113 | ||||||
| chr2:214734188
|
G | T | 13 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(10): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1904-3680C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214734188 | ||||||
| chr2:214734326
|
G | A | 13 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(10): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1904-3818C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214734326 | ||||||
| chr2:214734365
|
A | T | 38 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(35): Show | 40 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1904-3857T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214734365 | ||||||
| chr2:214734376
|
T | C | 2 | a0003c0005t0035g0257a0003c0005t0035g0259 | 2 | NA18951.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1904-3868A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214734376 | ||||||
| chr2:214734709
|
A | C | 62 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(59): Show | 67 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1904-4201T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214734709 | ||||||
| chr2:214734715
|
A | G | 4 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1904-4207T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214734715 | ||||||
| chr2:214734835
|
A | G | 3 | a0011c0014t0015g0005a0011c0014t0015g0118a0011c0014t0015g0119 | 4 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1904-4327T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214734835 | ||||||
| chr2:214734872
|
T | C | 2 | a0001c0004t0057g0278a0015c0028t0067g0241 | 2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1904-4364A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214734872 | ||||||
| chr2:214735212
|
T | A | 314 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(311): Show | 336 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(333): Show |
intron_variant | MODIFIER | c.1904-4704A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214735212 | ||||||
| chr2:214735335
|
G | A | 2 | a0009c0011t0069g0336a0009c0011t0070g0337 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1904-4827C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214735335 | ||||||
| chr2:214735335
|
G | GT | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1904-4828dupA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214735335 | ||||||
| chr2:214735356
|
T | C | 337 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(334): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.1904-4848A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214735356 | ||||||
| chr2:214735533
|
G | A | 142 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(139): Show | 150 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1904-5025C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214735533 | ||||||
| chr2:214735540
|
A | G | 1 | a0001c0004t0057g0278 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1904-5032T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214735540 | ||||||
| chr2:214735547
|
A | G | 10 | a0008c0009t0021g0015a0008c0009t0021g0223a0008c0009t0025g0266others(7): Show | 12 | HG01109.hp2 HG02055.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1904-5039T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214735547 | ||||||
| chr2:214735552
|
G | A | 13 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(10): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1904-5044C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214735552 | ||||||
| chr2:214735739
|
A | G | 2 | a0001c0004t0009g0125a0001c0004t0051g0230 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1904-5231T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214735739 | ||||||
| chr2:214735913
|
G | A | 62 | a0001c0002t0013g0276a0001c0002t0013g0322a0001c0003t0005g0043others(59): Show | 66 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.1904-5405C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214735913 | ||||||
| chr2:214735916
|
T | C | 8 | a0004c0007t0068g0265a0005c0006t0020g0022a0005c0006t0020g0023others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1904-5408A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214735916 | ||||||
| chr2:214736043
|
C | T | 314 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(311): Show | 336 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(333): Show |
intron_variant | MODIFIER | c.1904-5535G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736043 | ||||||
| chr2:214736078
|
T | C | 8 | a0004c0007t0068g0265a0005c0006t0020g0022a0005c0006t0020g0023others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1904-5570A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736078 | ||||||
| chr2:214736121
|
G | A | 1 | a0009c0011t0047g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1904-5613C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736121 | ||||||
| chr2:214736186
|
T | C | 8 | a0004c0007t0068g0265a0005c0006t0020g0022a0005c0006t0020g0023others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1904-5678A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736186 | ||||||
| chr2:214736227
|
G | C | 2 | a0005c0006t0046g0035a0009c0011t0032g0115 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1904-5719C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736227 | ||||||
| chr2:214736277
|
A | T | 1 | a0003c0005t0034g0255 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1904-5769T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736277 | ||||||
| chr2:214736283
|
T | C | 13 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(10): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1904-5775A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736283 | ||||||
| chr2:214736304
|
A | C | 13 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(10): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1904-5796T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736304 | ||||||
| chr2:214736383
|
G | A | 10 | a0008c0009t0021g0015a0008c0009t0021g0223a0008c0009t0025g0266others(7): Show | 12 | HG01109.hp2 HG02055.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1904-5875C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736383 | ||||||
| chr2:214736482
|
G | A | 1 | a0001c0004t0008g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1904-5974C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736482 | ||||||
| chr2:214736634
|
C | G | 64 | a0001c0002t0013g0276a0001c0002t0013g0322a0001c0003t0005g0043others(61): Show | 68 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.1904-6126G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736634 | ||||||
| chr2:214736714
|
A | AG | 8 | a0004c0007t0068g0265a0005c0006t0020g0022a0005c0006t0020g0023others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1904-6207_1904-620 others(5): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736714 | ||||||
| chr2:214736749
|
G | A | 2 | a0011c0014t0015g0118a0011c0014t0015g0119 | 2 | HG01074.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1904-6241C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736749 | ||||||
| chr2:214736801
|
T | C | 2 | a0005c0006t0009g0117a0012c0013t0052g0226 | 2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1904-6293A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736801 | ||||||
| chr2:214736905
|
C | A | 145 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(142): Show | 154 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1904-6397G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736905 | ||||||
| chr2:214736987
|
G | C | 13 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(10): Show | 13 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1904-6479C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214736987 | ||||||
| chr2:214737026
|
G | A | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1904-6518C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737026 | ||||||
| chr2:214737086
|
G | C | 1 | a0001c0002t0062g0328 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1904-6578C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737086 | ||||||
| chr2:214737202
|
C | T | 8 | a0004c0007t0068g0265a0005c0006t0020g0022a0005c0006t0020g0023others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1904-6694G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737202 | ||||||
| chr2:214737292
|
G | A | 1 | a0002c0001t0002g0216 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1904-6784C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737292 | ||||||
| chr2:214737350
|
G | T | 23 | a0001c0004t0008g0103a0001c0004t0014g0006a0001c0004t0014g0032others(20): Show | 25 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.1904-6842C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737350 | ||||||
| chr2:214737440
|
T | A | 2 | a0001c0002t0003g0312a0002c0001t0007g0199 | 2 | HG02523.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1904-6932A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737440 | ||||||
| chr2:214737440
|
T | C | 9 | a0001c0002t0003g0002a0001c0002t0003g0283a0001c0002t0003g0288others(6): Show | 11 | HG02074.hp1 HG02080.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.1904-6932A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737440 | ||||||
| chr2:214737537
|
G | A | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1904-7029C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737537 | ||||||
| chr2:214737574
|
T | C | 8 | a0004c0007t0068g0265a0005c0006t0020g0022a0005c0006t0020g0023others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1904-7066A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737574 | ||||||
| chr2:214737659
|
T | A | 1 | a0003c0005t0034g0255 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1904-7151A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737659 | ||||||
| chr2:214737671
|
A | T | 1 | a0003c0005t0034g0255 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1904-7163T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737671 | ||||||
| chr2:214737731
|
A | T | 1 | a0003c0005t0034g0255 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1904-7223T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737731 | ||||||
| chr2:214737733
|
T | A | 1 | a0003c0005t0034g0255 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1904-7225A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737733 | ||||||
| chr2:214737735
|
A | C | 1 | a0003c0005t0034g0255 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1904-7227T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737735 | ||||||
| chr2:214737803
|
C | T | 1 | a0001c0003t0002g0092 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1903+7264G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737803 | ||||||
| chr2:214737947
|
G | GA | 11 | a0003c0005t0034g0255a0004c0007t0068g0265a0005c0006t0009g0117others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1903+7119dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214737947 | ||||||
| chr2:214738155
|
C | T | 48 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(45): Show | 52 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1903+6912G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738155 | ||||||
| chr2:214738176
|
C | A | 145 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(142): Show | 154 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1903+6891G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738176 | ||||||
| chr2:214738192
|
G | A | 2 | a0003c0005t0006g0243a0003c0005t0006g0249 | 2 | NA18943.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1903+6875C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738192 | ||||||
| chr2:214738225
|
C | A | 337 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(334): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.1903+6842G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738225 | ||||||
| chr2:214738265
|
G | A | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1903+6802C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738265 | ||||||
| chr2:214738284
|
C | G | 3 | a0004c0007t0013g0264a0004c0007t0013g0268a0004c0007t0013g0269 | 3 | HG01256.hp1 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1903+6783G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738284 | ||||||
| chr2:214738289
|
C | T | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1903+6778G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738289 | ||||||
| chr2:214738337
|
C | A | 8 | a0004c0007t0068g0265a0005c0006t0020g0022a0005c0006t0020g0023others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1903+6730G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738337 | ||||||
| chr2:214738422
|
G | A | 8 | a0004c0007t0068g0265a0005c0006t0020g0022a0005c0006t0020g0023others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1903+6645C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738422 | ||||||
| chr2:214738447
|
C | T | 5 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(2): Show | 5 | HG01256.hp1 HG02257.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903+6620G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738447 | ||||||
| chr2:214738479
|
G | C | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1903+6588C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738479 | ||||||
| chr2:214738485
|
T | C | 8 | a0004c0007t0068g0265a0005c0006t0020g0022a0005c0006t0020g0023others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1903+6582A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738485 | ||||||
| chr2:214738597
|
T | A | 8 | a0004c0007t0068g0265a0005c0006t0020g0022a0005c0006t0020g0023others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1903+6470A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738597 | ||||||
| chr2:214738614
|
A | T | 313 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(310): Show | 335 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.1903+6453T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738614 | ||||||
| chr2:214738689
|
A | G | 1 | a0001c0003t0002g0095 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1903+6378T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738689 | ||||||
| chr2:214738704
|
G | A | 5 | a0001c0002t0007g0056a0001c0003t0002g0054a0001c0003t0007g0042others(2): Show | 5 | NA18955.hp1 NA18966.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903+6363C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738704 | ||||||
| chr2:214738769
|
C | T | 44 | a0001c0002t0013g0276a0001c0002t0013g0322a0001c0003t0005g0043others(41): Show | 46 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1903+6298G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738769 | ||||||
| chr2:214738790
|
A | C | 4 | a0001c0002t0003g0299a0001c0002t0003g0311a0001c0002t0003g0323others(1): Show | 4 | HG01358.hp2 HG01433.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1903+6277T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738790 | ||||||
| chr2:214738873
|
G | A | 12 | a0003c0005t0005g0101a0003c0005t0006g0243a0003c0005t0006g0244others(9): Show | 12 | HG00621.hp2 HG01981.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.1903+6194C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738873 | ||||||
| chr2:214738924
|
C | T | 2 | a0001c0004t0011g0121a0002c0033t0001g0181 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1903+6143G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214738924 | ||||||
| chr2:214739080
|
T | A | 91 | a0001c0003t0001g0041a0001c0004t0011g0121a0001c0004t0018g0277others(88): Show | 99 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1903+5987A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739080 | ||||||
| chr2:214739157
|
G | A | 6 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(3): Show | 7 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903+5910C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739157 | ||||||
| chr2:214739165
|
T | C | 1 | a0001c0019t0056g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1903+5902A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739165 | ||||||
| chr2:214739243
|
T | TA | 7 | a0001c0003t0002g0057a0001c0003t0002g0058a0001c0003t0002g0087others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+5823dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739243 | ||||||
| chr2:214739244
|
A | T | 24 | a0001c0004t0008g0103a0001c0004t0014g0006a0001c0004t0014g0032others(21): Show | 26 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1903+5823T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739244 | ||||||
| chr2:214739281
|
A | G | 2 | a0005c0006t0046g0035a0009c0011t0032g0115 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1903+5786T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739281 | ||||||
| chr2:214739300
|
G | A | 83 | a0001c0003t0001g0041a0001c0004t0011g0121a0002c0001t0001g0001others(80): Show | 91 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1903+5767C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739300 | ||||||
| chr2:214739306
|
C | A | 7 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+5761G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739306 | ||||||
| chr2:214739311
|
G | A | 7 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+5756C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739311 | ||||||
| chr2:214739352
|
T | A | 2 | a0002c0001t0009g0139a0019c0026t0025g0331 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1903+5715A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739352 | ||||||
| chr2:214739423
|
T | C | 7 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+5644A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739423 | ||||||
| chr2:214739458
|
T | A | 7 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+5609A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739458 | ||||||
| chr2:214739475
|
T | G | 39 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(36): Show | 41 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1903+5592A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739475 | ||||||
| chr2:214739528
|
C | A | 277 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(274): Show | 297 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.1903+5539G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739528 | ||||||
| chr2:214739563
|
G | GA | 7 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+5503dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739563 | ||||||
| chr2:214739811
|
G | A | 6 | a0001c0002t0003g0018a0001c0002t0003g0275a0001c0002t0003g0315others(3): Show | 7 | HG02129.hp2 NA18939.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+5256C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214739811 | ||||||
| chr2:214740027
|
A | G | 7 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+5040T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740027 | ||||||
| chr2:214740045
|
A | G | 2 | a0001c0002t0003g0287a0001c0002t0059g0318 | 2 | HG02165.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1903+5022T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740045 | ||||||
| chr2:214740166
|
A | C | 1 | a0001c0004t0009g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1903+4901T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740166 | ||||||
| chr2:214740327
|
C | T | 7 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+4740G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740327 | ||||||
| chr2:214740399
|
TATTA | T | 102 | a0001c0003t0001g0041a0001c0004t0011g0121a0001c0004t0018g0277others(99): Show | 110 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1903+4664_1903+466 others(8): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740399 | ||||||
| chr2:214740471
|
A | G | 4 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1903+4596T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740471 | ||||||
| chr2:214740493
|
C | G | 4 | a0005c0006t0046g0035a0009c0011t0032g0025a0009c0011t0032g0115others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1903+4574G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740493 | ||||||
| chr2:214740597
|
C | T | 143 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(140): Show | 151 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1903+4470G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740597 | ||||||
| chr2:214740679
|
G | C | 2 | a0004c0007t0013g0268a0004c0007t0013g0269 | 2 | HG01256.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1903+4388C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740679 | ||||||
| chr2:214740718
|
C | G | 1 | a0001c0004t0009g0110 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1903+4349G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740718 | ||||||
| chr2:214740764
|
G | C | 7 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+4303C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740764 | ||||||
| chr2:214740774
|
C | T | 13 | a0003c0005t0005g0101a0003c0005t0006g0243a0003c0005t0006g0244others(10): Show | 13 | HG00621.hp2 HG01981.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1903+4293G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740774 | ||||||
| chr2:214740782
|
A | G | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1903+4285T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740782 | ||||||
| chr2:214740822
|
T | A | 4 | a0001c0003t0002g0028a0001c0003t0002g0040a0001c0003t0002g0070others(1): Show | 4 | NA18943.hp2 NA18984.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1903+4245A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740822 | ||||||
| chr2:214740889
|
A | G | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1903+4178T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740889 | ||||||
| chr2:214740902
|
G | A | 7 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+4165C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740902 | ||||||
| chr2:214740903
|
T | TTTTG | 7 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+4163_1903+416 others(8): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740903 | ||||||
| chr2:214740974
|
C | G | 7 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+4093G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740974 | ||||||
| chr2:214740992
|
A | C | 155 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(152): Show | 166 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.1903+4075T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214740992 | ||||||
| chr2:214741141
|
C | T | 7 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+3926G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214741141 | ||||||
| chr2:214741241
|
T | C | 1 | a0004c0007t0058g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1903+3826A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214741241 | ||||||
| chr2:214741313
|
C | T | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1903+3754G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214741313 | ||||||
| chr2:214741514
|
C | A | 4 | a0005c0006t0046g0035a0009c0011t0032g0025a0009c0011t0032g0115others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1903+3553G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214741514 | ||||||
| chr2:214741570
|
G | A | 1 | a0002c0001t0011g0137 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1903+3497C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214741570 | ||||||
| chr2:214741572
|
T | C | 5 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(2): Show | 5 | HG01256.hp1 HG02257.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903+3495A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214741572 | ||||||
| chr2:214741608
|
T | C | 2 | a0002c0001t0001g0129a0002c0001t0045g0130 | 2 | NA18945.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1903+3459A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214741608 | ||||||
| chr2:214741611
|
G | A | 2 | a0001c0004t0009g0112a0001c0004t0009g0113 | 2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1903+3456C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214741611 | ||||||
| chr2:214741823
|
T | C | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1903+3244A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214741823 | ||||||
| chr2:214741909
|
T | C | 1 | a0001c0004t0009g0110 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1903+3158A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214741909 | ||||||
| chr2:214741926
|
TA | T | 168 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(165): Show | 180 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1903+3140delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214741926 | ||||||
| chr2:214741958
|
A | C | 7 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903+3109T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214741958 | ||||||
| chr2:214742002
|
A | G | 337 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(334): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.1903+3065T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214742002 | ||||||
| chr2:214742097
|
T | C | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1903+2970A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214742097 | ||||||
| chr2:214742381
|
G | A | 1 | a0019c0026t0025g0331 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1903+2686C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214742381 | ||||||
| chr2:214742425
|
C | T | 10 | a0002c0001t0001g0007a0002c0001t0001g0138a0002c0001t0001g0140others(7): Show | 11 | HG01891.hp2 HG01975.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1903+2642G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214742425 | ||||||
| chr2:214742580
|
A | G | 11 | a0003c0005t0005g0101a0003c0005t0006g0244a0003c0005t0006g0248others(8): Show | 11 | HG00621.hp2 HG01981.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.1903+2487T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214742580 | ||||||
| chr2:214742734
|
T | C | 176 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(173): Show | 188 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1903+2333A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214742734 | ||||||
| chr2:214742736
|
G | C | 176 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(173): Show | 188 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1903+2331C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214742736 | ||||||
| chr2:214742846
|
C | T | 12 | a0001c0002t0013g0276a0001c0002t0013g0322a0001c0004t0009g0004others(9): Show | 13 | HG01256.hp1 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1903+2221G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214742846 | ||||||
| chr2:214742875
|
C | T | 176 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(173): Show | 188 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1903+2192G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214742875 | ||||||
| chr2:214742902
|
C | T | 3 | a0011c0014t0015g0005a0011c0014t0015g0118a0011c0014t0015g0119 | 4 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1903+2165G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214742902 | ||||||
| chr2:214742933
|
T | C | 1 | a0001c0002t0003g0329 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1903+2134A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214742933 | ||||||
| chr2:214743132
|
T | A | 176 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(173): Show | 188 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1903+1935A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743132 | ||||||
| chr2:214743156
|
G | A | 1 | a0002c0001t0001g0008 | 2 | HG03239.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1903+1911C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743156 | ||||||
| chr2:214743172
|
A | G | 176 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(173): Show | 188 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1903+1895T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743172 | ||||||
| chr2:214743254
|
T | A | 176 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(173): Show | 188 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1903+1813A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743254 | ||||||
| chr2:214743333
|
C | T | 1 | a0001c0003t0002g0107 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1903+1734G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743333 | ||||||
| chr2:214743468
|
C | T | 1 | a0001c0004t0033g0237 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1903+1599G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743468 | ||||||
| chr2:214743592
|
A | AT | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1903+1474dupA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743592 | ||||||
| chr2:214743657
|
C | T | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1903+1410G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743657 | ||||||
| chr2:214743677
|
G | A | 3 | a0004c0007t0008g0031a0004c0007t0008g0033a0004c0007t0030g0034 | 3 | HG01069.hp2 HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1903+1390C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743677 | ||||||
| chr2:214743704
|
CT | C | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1903+1362delA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743704 | ||||||
| chr2:214743768
|
C | G | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1903+1299G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743768 | ||||||
| chr2:214743811
|
C | T | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1903+1256G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743811 | ||||||
| chr2:214743812
|
G | A | 1 | a0001c0002t0003g0272 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1903+1255C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743812 | ||||||
| chr2:214743858
|
C | A | 1 | a0001c0003t0002g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1903+1209G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743858 | ||||||
| chr2:214743914
|
T | C | 1 | a0001c0003t0010g0044 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1903+1153A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743914 | ||||||
| chr2:214743956
|
T | C | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1903+1111A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214743956 | ||||||
| chr2:214744079
|
T | C | 2 | a0001c0002t0013g0276a0001c0002t0013g0322 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1903+988A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214744079 | ||||||
| chr2:214744149
|
C | T | 1 | a0003c0005t0006g0251 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1903+918G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214744149 | ||||||
| chr2:214744410
|
T | G | 1 | a0002c0001t0001g0146 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1903+657A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214744410 | ||||||
| chr2:214744585
|
A | G | 2 | a0001c0003t0002g0054a0001c0003t0007g0082 | 2 | NA18989.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1903+482T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214744585 | ||||||
| chr2:214744779
|
C | T | 1 | a0001c0004t0009g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1903+288G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214744779 | ||||||
| chr2:214744780
|
G | A | 58 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(55): Show | 62 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1903+287C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214744780 | ||||||
| chr2:214744792
|
G | A | 1 | a0001c0022t0003g0271 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1903+275C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214744792 | ||||||
| chr2:214744841
|
C | A | 6 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(3): Show | 7 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903+226G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214744841 | ||||||
| chr2:214744846
|
T | C | 21 | a0001c0004t0008g0103a0001c0004t0014g0006a0001c0004t0014g0032others(18): Show | 23 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1903+221A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214744846 | ||||||
| chr2:214744872
|
C | A | 1 | a0001c0004t0009g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1903+195G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214744872 | ||||||
| chr2:214744921
|
A | G | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1903+146T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214744921 | ||||||
| chr2:214744922
|
C | T | 2 | a0001c0004t0009g0112a0001c0004t0009g0113 | 2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1903+145G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214744922 | ||||||
| chr2:214744969
|
G | A | 2 | a0002c0001t0001g0196a0002c0001t0001g0197 | 2 | HG00733.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1903+98C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 9/10 | chr2 | 214744969 | ||||||
| chr2:214745228
|
A | G | 12 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(9): Show | 12 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1811-69T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 8/10 | chr2 | 214745228 | ||||||
| chr2:214745236
|
T | C | 5 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(2): Show | 5 | HG01256.hp1 HG02257.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1811-77A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 8/10 | chr2 | 214745236 | ||||||
| chr2:214745246
|
G | C | 4 | a0005c0006t0046g0035a0009c0011t0032g0025a0009c0011t0032g0115others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1811-87C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 8/10 | chr2 | 214745246 | ||||||
| chr2:214745401
|
A | G | 4 | a0005c0006t0046g0035a0009c0011t0032g0025a0009c0011t0032g0115others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1811-242T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 8/10 | chr2 | 214745401 | ||||||
| chr2:214745569
|
T | G | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1810+153A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 8/10 | chr2 | 214745569 | ||||||
| chr2:214745589
|
G | T | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1810+133C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 8/10 | chr2 | 214745589 | ||||||
| chr2:214745623
|
A | G | 2 | a0001c0004t0009g0125a0001c0004t0051g0230 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1810+99T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 8/10 | chr2 | 214745623 | ||||||
| chr2:214745985
|
A | G | 1 | a0001c0003t0002g0028 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1678-131T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214745985 | ||||||
| chr2:214746016
|
A | T | 298 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(295): Show | 320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.1678-162T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746016 | ||||||
| chr2:214746053
|
T | C | 90 | a0001c0003t0001g0041a0001c0004t0011g0121a0002c0001t0001g0001others(87): Show | 98 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1678-199A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746053 | ||||||
| chr2:214746105
|
G | T | 1 | a0001c0002t0063g0326 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1678-251C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746105 | ||||||
| chr2:214746187
|
G | A | 9 | a0001c0004t0009g0125a0001c0004t0051g0230a0008c0009t0021g0015others(6): Show | 11 | HG01109.hp2 HG02055.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1678-333C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746187 | ||||||
| chr2:214746300
|
T | A | 1 | a0004c0007t0058g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1678-446A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746300 | ||||||
| chr2:214746426
|
T | C | 1 | a0001c0003t0031g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1678-572A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746426 | ||||||
| chr2:214746436
|
G | A | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1678-582C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746436 | ||||||
| chr2:214746508
|
C | T | 2 | a0001c0004t0018g0280a0001c0004t0018g0281 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1678-654G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746508 | ||||||
| chr2:214746591
|
CAT | C | 147 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(144): Show | 155 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1678-739_1678-738d others(4): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746591 | ||||||
| chr2:214746700
|
T | C | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1678-846A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746700 | ||||||
| chr2:214746764
|
G | C | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1678-910C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746764 | ||||||
| chr2:214746924
|
C | A | 4 | a0005c0006t0046g0035a0009c0011t0032g0025a0009c0011t0032g0115others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678-1070G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746924 | ||||||
| chr2:214746926
|
G | A | 6 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(3): Show | 7 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1678-1072C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746926 | ||||||
| chr2:214746986
|
A | G | 3 | a0004c0007t0058g0263a0008c0009t0025g0266a0008c0009t0025g0267 | 3 | HG02486.hp1 HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1678-1132T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214746986 | ||||||
| chr2:214747092
|
A | G | 1 | a0005c0006t0020g0022 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1678-1238T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747092 | ||||||
| chr2:214747151
|
G | A | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1678-1297C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747151 | ||||||
| chr2:214747279
|
T | A | 7 | a0008c0009t0021g0015a0008c0009t0021g0223a0008c0009t0049g0222others(4): Show | 9 | HG01109.hp2 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678-1425A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747279 | ||||||
| chr2:214747321
|
G | A | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1678-1467C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747321 | ||||||
| chr2:214747326
|
T | C | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1678-1472A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747326 | ||||||
| chr2:214747365
|
C | T | 1 | a0001c0002t0003g0321 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1678-1511G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747365 | ||||||
| chr2:214747381
|
G | A | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1678-1527C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747381 | ||||||
| chr2:214747407
|
G | A | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1678-1553C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747407 | ||||||
| chr2:214747416
|
C | T | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1678-1562G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747416 | ||||||
| chr2:214747419
|
C | T | 39 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(36): Show | 41 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1678-1565G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747419 | ||||||
| chr2:214747424
|
C | G | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1678-1570G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747424 | ||||||
| chr2:214747545
|
T | C | 2 | a0002c0001t0001g0208a0006c0008t0001g0206 | 2 | NA19001.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1678-1691A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747545 | ||||||
| chr2:214747670
|
C | G | 2 | a0005c0006t0046g0035a0009c0011t0032g0115 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1678-1816G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747670 | ||||||
| chr2:214747671
|
A | G | 2 | a0005c0006t0046g0035a0009c0011t0032g0115 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1678-1817T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747671 | ||||||
| chr2:214747691
|
C | T | 1 | a0013c0017t0008g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1678-1837G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747691 | ||||||
| chr2:214747744
|
A | C | 3 | a0008c0009t0021g0015a0008c0009t0021g0223a0008c0009t0049g0222 | 4 | HG01109.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678-1890T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747744 | ||||||
| chr2:214747781
|
C | G | 39 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(36): Show | 41 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1678-1927G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747781 | ||||||
| chr2:214747796
|
T | A | 1 | a0008c0009t0025g0266 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1678-1942A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747796 | ||||||
| chr2:214747818
|
G | T | 2 | a0005c0006t0020g0022a0005c0006t0020g0023 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1678-1964C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747818 | ||||||
| chr2:214747859
|
T | TAATAA | 4 | a0002c0001t0001g0010a0002c0001t0001g0184a0002c0001t0001g0185others(1): Show | 5 | NA18953.hp2 NA18989.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678-2010_1678-200 others(9): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747859 | ||||||
| chr2:214747899
|
A | T | 19 | a0001c0004t0008g0103a0001c0004t0014g0006a0001c0004t0014g0032others(16): Show | 21 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1678-2045T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747899 | ||||||
| chr2:214747950
|
T | C | 1 | a0001c0003t0028g0062 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1678-2096A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214747950 | ||||||
| chr2:214748305
|
T | C | 2 | a0001c0002t0013g0276a0001c0002t0013g0322 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1678-2451A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214748305 | ||||||
| chr2:214748354
|
G | A | 1 | a0011c0014t0015g0119 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1678-2500C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214748354 | ||||||
| chr2:214748370
|
A | G | 15 | a0001c0002t0013g0276a0001c0002t0013g0322a0001c0004t0009g0004others(12): Show | 17 | HG01074.hp2 HG01256.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1678-2516T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214748370 | ||||||
| chr2:214748415
|
T | C | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1678-2561A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214748415 | ||||||
| chr2:214748514
|
TA | T | 2 | a0001c0002t0003g0020a0001c0002t0003g0319 | 3 | HG03831.hp1 NA20905.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1678-2661delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214748514 | ||||||
| chr2:214748525
|
GA | G | 9 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(6): Show | 10 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1678-2672delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214748525 | ||||||
| chr2:214748537
|
A | C | 6 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(3): Show | 7 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1678-2683T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214748537 | ||||||
| chr2:214748566
|
CACAA | C | 5 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(2): Show | 5 | HG01256.hp1 HG02257.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678-2716_1678-271 others(8): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214748566 | ||||||
| chr2:214748718
|
C | G | 152 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(149): Show | 162 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1678-2864G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214748718 | ||||||
| chr2:214748877
|
C | CACTT | 277 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(274): Show | 297 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.1678-3024_1678-302 others(8): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214748877 | ||||||
| chr2:214748947
|
C | T | 1 | a0004c0007t0036g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1678-3093G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214748947 | ||||||
| chr2:214749133
|
C | G | 3 | a0005c0006t0046g0035a0009c0011t0032g0115a0009c0011t0047g0116 | 3 | HG03041.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1678-3279G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214749133 | ||||||
| chr2:214749183
|
GA | G | 171 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(168): Show | 182 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.1677+3263delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214749183 | ||||||
| chr2:214749183
|
GAA | G | 6 | a0001c0019t0056g0330a0002c0001t0009g0139a0004c0007t0058g0263others(3): Show | 6 | HG02486.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1677+3262_1677+326 others(6): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214749183 | ||||||
| chr2:214749289
|
G | A | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1677+3158C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214749289 | ||||||
| chr2:214749291
|
G | A | 1 | a0001c0002t0003g0311 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1677+3156C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214749291 | ||||||
| chr2:214749462
|
A | G | 2 | a0001c0002t0003g0334a0001c0002t0003g0335 | 2 | NA18972.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1677+2985T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214749462 | ||||||
| chr2:214749489
|
C | T | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1677+2958G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214749489 | ||||||
| chr2:214749504
|
C | G | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1677+2943G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214749504 | ||||||
| chr2:214749782
|
CTT | C | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1677+2663_1677+266 others(6): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214749782 | ||||||
| chr2:214749833
|
T | C | 1 | a0001c0002t0003g0272 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1677+2614A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214749833 | ||||||
| chr2:214749960
|
T | C | 1 | a0001c0003t0002g0076 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1677+2487A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214749960 | ||||||
| chr2:214749985
|
C | G | 6 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1677+2462G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214749985 | ||||||
| chr2:214750072
|
C | T | 19 | a0001c0004t0008g0103a0001c0004t0014g0006a0001c0004t0014g0032others(16): Show | 21 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1677+2375G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214750072 | ||||||
| chr2:214750164
|
T | C | 1 | a0001c0004t0017g0232 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1677+2283A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214750164 | ||||||
| chr2:214750169
|
CTCT | C | 6 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1677+2275_1677+227 others(7): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214750169 | ||||||
| chr2:214750186
|
A | G | 1 | a0003c0005t0006g0244 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1677+2261T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214750186 | ||||||
| chr2:214750207
|
A | G | 1 | a0001c0002t0004g0297 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1677+2240T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214750207 | ||||||
| chr2:214750280
|
T | A | 3 | a0004c0007t0013g0264a0004c0007t0013g0268a0004c0007t0013g0269 | 3 | HG01256.hp1 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1677+2167A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214750280 | ||||||
| chr2:214750601
|
A | G | 1 | a0001c0002t0004g0291 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1677+1846T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214750601 | ||||||
| chr2:214750657
|
A | T | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1677+1790T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214750657 | ||||||
| chr2:214750731
|
C | G | 1 | a0007c0015t0002g0220 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1677+1716G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214750731 | ||||||
| chr2:214750835
|
C | T | 7 | a0008c0009t0021g0015a0008c0009t0021g0223a0008c0009t0049g0222others(4): Show | 9 | HG01109.hp2 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1677+1612G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214750835 | ||||||
| chr2:214751037
|
T | C | 1 | a0004c0007t0058g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1677+1410A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751037 | ||||||
| chr2:214751079
|
C | CTGTG | 4 | a0003c0005t0055g0245a0004c0007t0008g0033a0004c0007t0008g0126others(1): Show | 4 | HG01069.hp2 HG02293.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1677+1364_1677+136 others(8): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751079 | ||||||
| chr2:214751079
|
C | CTGTGTGT others(3): Show |
1 | a0004c0007t0036g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1677+1358_1677+136 others(14): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751079 | ||||||
| chr2:214751079
|
CTG | C | 3 | a0001c0003t0005g0066a0001c0003t0005g0096a0003c0005t0005g0101 | 3 | HG02300.hp2 NA18946.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1677+1366_1677+136 others(6): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751079 | ||||||
| chr2:214751079
|
CTGTG | C | 3 | a0002c0001t0001g0135a0002c0001t0001g0136a0005c0006t0001g0036 | 3 | HG02683.hp2 HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1677+1364_1677+136 others(8): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751079 | ||||||
| chr2:214751079
|
CTGTGTG | C | 5 | a0001c0004t0018g0277a0002c0001t0001g0133a0002c0001t0001g0134others(2): Show | 5 | HG01256.hp2 HG01258.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1677+1362_1677+136 others(10): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751079 | ||||||
| chr2:214751079
|
CTGTGTGT others(1): Show |
C | 11 | a0001c0004t0018g0279a0001c0004t0018g0281a0002c0001t0005g0207others(8): Show | 12 | HG00609.hp2 HG02622.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1677+1360_1677+136 others(12): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751079 | ||||||
| chr2:214751079
|
CTGTGTGT others(3): Show |
C | 1 | a0019c0026t0025g0331 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1677+1358_1677+136 others(14): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751079 | ||||||
| chr2:214751079
|
CTGTGTGT others(5): Show |
C | 5 | a0003c0005t0006g0273a0003c0005t0006g0274a0005c0006t0020g0022others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1677+1356_1677+136 others(16): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751079 | ||||||
| chr2:214751081
|
G | C | 172 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(169): Show | 184 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1677+1366C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751081 | ||||||
| chr2:214751083
|
G | C | 14 | a0001c0002t0013g0276a0001c0002t0013g0322a0001c0004t0009g0004others(11): Show | 15 | HG01256.hp1 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1677+1364C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751083 | ||||||
| chr2:214751085
|
G | C | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1677+1362C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751085 | ||||||
| chr2:214751093
|
G | C | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1677+1354C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751093 | ||||||
| chr2:214751095
|
G | C | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1677+1352C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751095 | ||||||
| chr2:214751097
|
G | C | 1 | a0005c0006t0020g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1677+1350C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751097 | ||||||
| chr2:214751101
|
GTGTGTGT others(11): Show |
G | 1 | a0005c0006t0046g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1677+1328_1677+134 others(22): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751101 | ||||||
| chr2:214751101
|
GTGTGTGT others(17): Show |
G | 31 | a0001c0002t0003g0283a0001c0002t0003g0308a0001c0002t0003g0315others(28): Show | 32 | HG00408.hp1 HG00438.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1677+1322_1677+134 others(28): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751101 | ||||||
| chr2:214751101
|
GTGTGTGT others(19): Show |
G | 109 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(106): Show | 115 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.1677+1320_1677+134 others(30): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751101 | ||||||
| chr2:214751101
|
GTGTGTGT others(21): Show |
G | 7 | a0008c0009t0021g0015a0008c0009t0021g0223a0008c0009t0049g0222others(4): Show | 9 | HG01109.hp2 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1677+1318_1677+134 others(32): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751101 | ||||||
| chr2:214751101
|
GTGTGTGT others(23): Show |
G | 5 | a0001c0004t0009g0004a0001c0004t0009g0111a0011c0014t0015g0005others(2): Show | 7 | HG01074.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1677+1316_1677+134 others(34): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751101 | ||||||
| chr2:214751101
|
GTGTGTGT others(25): Show |
G | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1677+1314_1677+134 others(36): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751101 | ||||||
| chr2:214751103
|
GTGTGTGT others(15): Show |
G | 1 | a0016c0023t0004g0294 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1677+1322_1677+134 others(26): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751103 | ||||||
| chr2:214751103
|
GTGTGTGT others(17): Show |
G | 8 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0002g0054others(5): Show | 9 | HG01255.hp1 HG01516.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1677+1320_1677+134 others(28): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751103 | ||||||
| chr2:214751103
|
GTGTGTGT others(23): Show |
G | 4 | a0001c0002t0013g0276a0001c0004t0009g0109a0001c0004t0009g0110others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1677+1314_1677+134 others(34): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751103 | ||||||
| chr2:214751103
|
GTGTGTGT others(25): Show |
G | 2 | a0001c0002t0013g0322a0001c0004t0009g0113 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1677+1312_1677+134 others(36): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751103 | ||||||
| chr2:214751103
|
GTGTGTGT others(27): Show |
G | 3 | a0004c0007t0013g0264a0004c0007t0013g0268a0004c0007t0013g0269 | 3 | HG01256.hp1 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1677+1310_1677+134 others(38): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751103 | ||||||
| chr2:214751105
|
GTGTGTGT others(7): Show |
G | 2 | a0001c0003t0005g0073a0001c0003t0005g0080 | 2 | HG02004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1677+1328_1677+134 others(18): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751105 | ||||||
| chr2:214751107
|
G | A | 8 | a0001c0003t0005g0043a0001c0003t0005g0065a0001c0003t0005g0108others(5): Show | 8 | HG00735.hp2 HG03942.hp2 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.1677+1340C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751107 | ||||||
| chr2:214751107
|
GTGTGTGT others(5): Show |
G | 2 | a0005c0006t0009g0117a0014c0016t0005g0200 | 2 | HG03098.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1677+1328_1677+133 others(16): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751107 | ||||||
| chr2:214751107
|
GTGTGTGT others(9): Show |
G | 1 | a0002c0001t0009g0139 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1677+1324_1677+133 others(20): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751107 | ||||||
| chr2:214751107
|
GTGTGTGT others(17): Show |
G | 2 | a0001c0004t0057g0278a0003c0005t0041g0026 | 2 | HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1677+1316_1677+133 others(28): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751107 | ||||||
| chr2:214751109
|
G | A | 21 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(18): Show | 22 | HG00621.hp2 HG00735.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1677+1338C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751109 | ||||||
| chr2:214751109
|
GTGTGTGT others(3): Show |
G | 2 | a0001c0004t0018g0280a0009c0011t0070g0337 | 2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1677+1328_1677+133 others(14): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751109 | ||||||
| chr2:214751111
|
G | A | 24 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(21): Show | 25 | HG00621.hp2 HG00735.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.1677+1336C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751111 | ||||||
| chr2:214751111
|
GTGTGTGT others(1): Show |
G | 9 | a0002c0001t0001g0007a0002c0001t0001g0127a0002c0001t0001g0140others(6): Show | 10 | HG01346.hp2 HG01934.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1677+1328_1677+133 others(12): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751111 | ||||||
| chr2:214751111
|
GTGTGTGT others(3): Show |
G | 39 | a0001c0003t0001g0041a0002c0001t0001g0008a0002c0001t0001g0009others(36): Show | 42 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1677+1326_1677+133 others(14): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751111 | ||||||
| chr2:214751111
|
GTGTGTGT others(5): Show |
G | 11 | a0002c0001t0001g0001a0002c0001t0001g0010a0002c0001t0001g0151others(8): Show | 15 | HG00438.hp1 HG01081.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1677+1324_1677+133 others(16): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751111 | ||||||
| chr2:214751111
|
GTGTGTGT others(7): Show |
G | 1 | a0002c0001t0001g0132 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1677+1322_1677+133 others(18): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751111 | ||||||
| chr2:214751111
|
GTGTGTGT others(9): Show |
G | 1 | a0002c0001t0001g0208 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1677+1320_1677+133 others(20): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751111 | ||||||
| chr2:214751111
|
GTGTGTGT others(11): Show |
G | 1 | a0006c0008t0001g0206 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1677+1318_1677+133 others(22): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751111 | ||||||
| chr2:214751113
|
G | A | 25 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(22): Show | 26 | HG00621.hp2 HG00735.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.1677+1334C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751113 | ||||||
| chr2:214751113
|
GTGTGTAT others(1): Show |
G | 3 | a0002c0001t0001g0156a0002c0001t0001g0212a0005c0006t0066g0333 | 3 | HG01071.hp2 HG02132.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1677+1326_1677+133 others(12): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751113 | ||||||
| chr2:214751113
|
GTGTGTAT others(3): Show |
G | 3 | a0002c0001t0001g0129a0002c0001t0038g0160a0002c0001t0045g0130 | 3 | HG03453.hp2 NA18945.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1677+1324_1677+133 others(14): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751113 | ||||||
| chr2:214751115
|
G | A | 32 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(29): Show | 33 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1677+1332C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751115 | ||||||
| chr2:214751115
|
GTGTATAT others(7): Show |
G | 3 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228 | 3 | HG02818.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1677+1318_1677+133 others(18): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751115 | ||||||
| chr2:214751117
|
G | A | 43 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(40): Show | 45 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1677+1330C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751117 | ||||||
| chr2:214751117
|
G | GTGTGTAT others(5): Show |
1 | a0004c0010t0030g0104 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1677+1329_1677+133 others(16): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751117 | ||||||
| chr2:214751117
|
G | GTGTGTAT others(7): Show |
1 | a0004c0010t0008g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1677+1329_1677+133 others(18): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751117 | ||||||
| chr2:214751117
|
G | GTGTGTAT others(9): Show |
1 | a0004c0010t0008g0003 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1677+1329_1677+133 others(20): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751117 | ||||||
| chr2:214751117
|
G | GTGTGTGT others(5): Show |
1 | a0004c0010t0008g0106 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1677+1329_1677+133 others(16): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751117 | ||||||
| chr2:214751117
|
G | GTGTGTGT others(9): Show |
1 | a0004c0007t0008g0031 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1677+1329_1677+133 others(20): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751117 | ||||||
| chr2:214751117
|
GTATATAT others(3): Show |
G | 1 | a0012c0013t0052g0226 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1677+1320_1677+132 others(14): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751117 | ||||||
| chr2:214751119
|
A | G | 6 | a0001c0004t0008g0103a0001c0004t0014g0032a0001c0004t0027g0123others(3): Show | 6 | HG00741.hp2 HG01361.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1677+1328T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751119 | ||||||
| chr2:214751121
|
A | G | 5 | a0001c0004t0011g0121a0001c0004t0014g0032a0001c0004t0027g0124others(2): Show | 5 | HG01361.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1677+1326T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751121 | ||||||
| chr2:214751123
|
A | G | 5 | a0001c0004t0011g0121a0001c0004t0014g0032a0002c0033t0001g0181others(2): Show | 5 | HG01361.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1677+1324T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751123 | ||||||
| chr2:214751125
|
A | G | 2 | a0001c0004t0011g0121a0002c0033t0001g0181 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1677+1322T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751125 | ||||||
| chr2:214751129
|
A | G | 32 | a0001c0002t0003g0283a0001c0002t0003g0308a0001c0002t0003g0315others(29): Show | 33 | HG00408.hp1 HG00438.hp2 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.1677+1318T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751129 | ||||||
| chr2:214751131
|
A | G | 115 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(112): Show | 122 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.1677+1316T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751131 | ||||||
| chr2:214751133
|
A | T | 1 | a0009c0011t0047g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1677+1314T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751133 | ||||||
| chr2:214751138
|
TATATATA others(2): Show |
T | 3 | a0002c0001t0001g0162a0002c0001t0001g0168a0002c0001t0011g0171 | 3 | HG02523.hp1 NA18939.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1677+1300_1677+130 others(13): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751138 | ||||||
| chr2:214751141
|
A | T | 1 | a0021c0024t0006g0247 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1677+1306T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751141 | ||||||
| chr2:214751142
|
T | C | 1 | a0001c0003t0031g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1677+1305A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751142 | ||||||
| chr2:214751142
|
TA | T | 8 | a0001c0003t0005g0073a0001c0003t0005g0080a0002c0001t0001g0213others(5): Show | 9 | HG02004.hp2 HG04184.hp2 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.1677+1304delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751142 | ||||||
| chr2:214751143
|
A | T | 7 | a0001c0003t0005g0043a0001c0003t0005g0065a0001c0003t0005g0096others(4): Show | 7 | HG01981.hp1 HG04199.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1677+1304T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751143 | ||||||
| chr2:214751144
|
TA | T | 16 | a0002c0001t0001g0127a0002c0001t0001g0133a0002c0001t0001g0136others(13): Show | 17 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1677+1302delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751144 | ||||||
| chr2:214751145
|
A | AT | 3 | a0003c0005t0035g0257a0008c0009t0025g0266a0014c0016t0029g0152 | 3 | HG02630.hp2 HG03942.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1677+1301dupA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751145 | ||||||
| chr2:214751145
|
A | T | 26 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(23): Show | 27 | HG01258.hp2 HG01978.hp1 HG01981.hp1 others(24): Show |
intron_variant | MODIFIER | c.1677+1302T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751145 | ||||||
| chr2:214751146
|
T | C | 24 | a0001c0002t0003g0283a0001c0002t0003g0308a0001c0002t0003g0315others(21): Show | 25 | HG00408.hp1 HG00438.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.1677+1301A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751146 | ||||||
| chr2:214751146
|
TA | T | 29 | a0001c0003t0001g0041a0002c0001t0001g0007a0002c0001t0001g0009others(26): Show | 31 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.1677+1300delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751146 | ||||||
| chr2:214751147
|
A | T | 57 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(54): Show | 61 | HG00621.hp2 HG00639.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.1677+1300T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751147 | ||||||
| chr2:214751148
|
T | C | 119 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(116): Show | 126 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.1677+1299A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751148 | ||||||
| chr2:214751148
|
TA | T | 28 | a0001c0002t0003g0283a0001c0002t0003g0308a0001c0002t0003g0315others(25): Show | 29 | HG00408.hp1 HG00438.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.1677+1298delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751148 | ||||||
| chr2:214751149
|
A | T | 115 | a0001c0003t0001g0041a0001c0003t0002g0075a0001c0003t0005g0043others(112): Show | 125 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1677+1298T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751149 | ||||||
| chr2:214751150
|
TA | T | 15 | a0001c0002t0003g0314a0001c0002t0024g0270a0001c0003t0002g0046others(12): Show | 15 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1677+1296delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751150 | ||||||
| chr2:214751151
|
A | ATATATAT others(22): Show |
1 | a0004c0007t0030g0034 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1677+1295_1677+129 others(33): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751151 | ||||||
| chr2:214751151
|
A | ATATATAT others(16): Show |
1 | a0004c0007t0008g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1677+1295_1677+129 others(27): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751151 | ||||||
| chr2:214751151
|
A | ATATATAT others(17): Show |
1 | a0004c0007t0008g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1677+1295_1677+129 others(28): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751151 | ||||||
| chr2:214751151
|
A | ATATATAT others(14): Show |
1 | a0004c0007t0008g0033 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1677+1295_1677+129 others(25): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751151 | ||||||
| chr2:214751151
|
A | ATATATAT others(14): Show |
1 | a0004c0007t0036g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1677+1295_1677+129 others(25): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751151 | ||||||
| chr2:214751151
|
A | ATATATTT others(4): Show |
1 | a0003c0005t0006g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1677+1295_1677+129 others(15): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751151 | ||||||
| chr2:214751151
|
A | ATATTTTT others(4): Show |
1 | a0013c0017t0008g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1677+1295_1677+129 others(15): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751151 | ||||||
| chr2:214751151
|
A | ATTTTTTT others(5): Show |
1 | a0004c0007t0008g0031 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1677+1284_1677+129 others(16): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751151 | ||||||
| chr2:214751151
|
A | ATTTTTTT others(6): Show |
1 | a0004c0010t0008g0106 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1677+1283_1677+129 others(17): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751151 | ||||||
| chr2:214751151
|
A | T | 260 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(257): Show | 278 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.1677+1296T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751151 | ||||||
| chr2:214751151
|
AT | A | 15 | a0001c0002t0013g0276a0001c0002t0013g0322a0001c0004t0009g0004others(12): Show | 18 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1677+1295delA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751151 | ||||||
| chr2:214751153
|
T | A | 6 | a0001c0004t0057g0278a0005c0006t0009g0117a0009c0011t0032g0115others(3): Show | 6 | HG01081.hp2 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1677+1294A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751153 | ||||||
| chr2:214751154
|
T | A | 2 | a0001c0004t0018g0277a0001c0004t0027g0123 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1677+1293A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751154 | ||||||
| chr2:214751155
|
T | A | 5 | a0001c0004t0014g0032a0005c0006t0009g0117a0009c0011t0047g0116others(2): Show | 5 | HG01081.hp2 HG03098.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1677+1292A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751155 | ||||||
| chr2:214751156
|
T | A | 1 | a0003c0005t0006g0274 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1677+1291A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751156 | ||||||
| chr2:214751160
|
T | A | 2 | a0005c0006t0020g0022a0005c0006t0020g0023 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1677+1287A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751160 | ||||||
| chr2:214751266
|
T | A | 1 | a0003c0005t0006g0273 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1677+1181A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751266 | ||||||
| chr2:214751306
|
T | A | 6 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1677+1141A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751306 | ||||||
| chr2:214751445
|
G | A | 4 | a0002c0001t0001g0196a0002c0001t0001g0197a0002c0001t0007g0150others(1): Show | 4 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1677+1002C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751445 | ||||||
| chr2:214751484
|
C | T | 6 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1677+963G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751484 | ||||||
| chr2:214751734
|
A | T | 5 | a0001c0004t0014g0006a0001c0004t0014g0032a0001c0004t0014g0122others(2): Show | 6 | HG02559.hp2 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1677+713T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751734 | ||||||
| chr2:214751838
|
C | T | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1677+609G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751838 | ||||||
| chr2:214751984
|
C | T | 174 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(171): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1677+463G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214751984 | ||||||
| chr2:214752078
|
T | C | 1 | a0004c0007t0008g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1677+369A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214752078 | ||||||
| chr2:214752130
|
A | G | 2 | a0001c0004t0009g0125a0001c0004t0051g0230 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1677+317T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214752130 | ||||||
| chr2:214752273
|
G | C | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1677+174C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214752273 | ||||||
| chr2:214752343
|
G | T | 6 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1677+104C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214752343 | ||||||
| chr2:214752358
|
T | G | 7 | a0008c0009t0021g0015a0008c0009t0021g0223a0008c0009t0049g0222others(4): Show | 9 | HG01109.hp2 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1677+89A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 7/10 | chr2 | 214752358 | ||||||
| chr2:214752611
|
T | C | 3 | a0011c0014t0015g0005a0011c0014t0015g0118a0011c0014t0015g0119 | 4 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1569-56A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214752611 | ||||||
| chr2:214752735
|
T | C | 1 | a0001c0003t0002g0088 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1569-180A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214752735 | ||||||
| chr2:214752739
|
C | T | 4 | a0001c0003t0002g0028a0001c0003t0002g0040a0001c0003t0002g0070others(1): Show | 4 | NA18943.hp2 NA18984.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1569-184G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214752739 | ||||||
| chr2:214752776
|
T | C | 90 | a0001c0003t0001g0041a0001c0004t0011g0121a0002c0001t0001g0001others(87): Show | 98 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1569-221A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214752776 | ||||||
| chr2:214752827
|
G | C | 1 | a0001c0003t0002g0079 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1569-272C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214752827 | ||||||
| chr2:214752841
|
A | C | 1 | a0001c0003t0002g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1569-286T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214752841 | ||||||
| chr2:214752848
|
A | G | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1569-293T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214752848 | ||||||
| chr2:214752851
|
A | C | 2 | a0002c0001t0002g0014a0002c0001t0002g0217 | 3 | HG01516.hp2 HG01517.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1569-296T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214752851 | ||||||
| chr2:214752945
|
C | T | 1 | a0005c0006t0066g0333 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1569-390G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214752945 | ||||||
| chr2:214753068
|
A | G | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1569-513T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214753068 | ||||||
| chr2:214753201
|
G | A | 1 | a0001c0002t0003g0288 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1569-646C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214753201 | ||||||
| chr2:214753229
|
A | G | 104 | a0001c0003t0001g0041a0001c0004t0011g0121a0001c0004t0018g0277others(101): Show | 112 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1569-674T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214753229 | ||||||
| chr2:214753396
|
T | C | 1 | a0011c0014t0015g0118 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1569-841A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214753396 | ||||||
| chr2:214753433
|
T | C | 1 | a0004c0007t0058g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1569-878A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214753433 | ||||||
| chr2:214753469
|
T | C | 2 | a0002c0001t0009g0139a0019c0026t0025g0331 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1569-914A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214753469 | ||||||
| chr2:214753639
|
G | A | 174 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(171): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1569-1084C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214753639 | ||||||
| chr2:214753668
|
A | G | 1 | a0004c0007t0058g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1569-1113T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214753668 | ||||||
| chr2:214753863
|
A | G | 151 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(148): Show | 161 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1569-1308T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214753863 | ||||||
| chr2:214753957
|
G | A | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1569-1402C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214753957 | ||||||
| chr2:214754055
|
A | G | 104 | a0001c0003t0001g0041a0001c0004t0011g0121a0001c0004t0018g0277others(101): Show | 112 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1569-1500T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754055 | ||||||
| chr2:214754071
|
C | T | 174 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(171): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1569-1516G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754071 | ||||||
| chr2:214754224
|
AAAC | A | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1569-1672_1569-167 others(7): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754224 | ||||||
| chr2:214754256
|
T | C | 1 | a0002c0001t0002g0014 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1569-1701A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754256 | ||||||
| chr2:214754319
|
G | T | 124 | a0001c0003t0001g0041a0001c0004t0008g0103a0001c0004t0011g0121others(121): Show | 134 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1569-1764C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754319 | ||||||
| chr2:214754356
|
GA | G | 8 | a0001c0019t0056g0330a0008c0009t0021g0015a0008c0009t0021g0223others(5): Show | 10 | HG01109.hp2 HG02055.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1569-1802delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754356 | ||||||
| chr2:214754367
|
A | T | 1 | a0009c0011t0047g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1569-1812T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754367 | ||||||
| chr2:214754420
|
C | CA | 12 | a0001c0002t0013g0276a0001c0002t0013g0322a0004c0007t0013g0264others(9): Show | 12 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1569-1866dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754420 | ||||||
| chr2:214754474
|
A | G | 2 | a0004c0007t0013g0268a0004c0007t0013g0269 | 2 | HG01256.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1569-1919T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754474 | ||||||
| chr2:214754595
|
T | G | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1569-2040A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754595 | ||||||
| chr2:214754763
|
C | T | 1 | a0013c0017t0002g0141 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1569-2208G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754763 | ||||||
| chr2:214754835
|
A | C | 1 | a0001c0003t0002g0067 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1569-2280T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754835 | ||||||
| chr2:214754837
|
T | C | 1 | a0001c0002t0062g0328 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1569-2282A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754837 | ||||||
| chr2:214754934
|
T | C | 174 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(171): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1569-2379A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754934 | ||||||
| chr2:214754955
|
T | C | 9 | a0001c0002t0003g0287a0001c0002t0004g0019a0001c0002t0004g0021others(6): Show | 11 | HG00408.hp1 HG02165.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.1569-2400A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754955 | ||||||
| chr2:214754980
|
G | GGAT | 7 | a0008c0009t0021g0015a0008c0009t0021g0223a0008c0009t0049g0222others(4): Show | 9 | HG01109.hp2 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1569-2426_1569-242 others(7): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754980 | ||||||
| chr2:214754983
|
G | A | 5 | a0001c0004t0014g0006a0001c0004t0014g0032a0001c0004t0014g0122others(2): Show | 6 | HG02559.hp2 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1569-2428C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754983 | ||||||
| chr2:214754989
|
G | T | 5 | a0002c0001t0001g0164a0002c0001t0001g0165a0002c0001t0001g0166others(2): Show | 5 | HG01346.hp2 NA18949.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1569-2434C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214754989 | ||||||
| chr2:214755071
|
G | C | 4 | a0005c0006t0046g0035a0009c0011t0032g0025a0009c0011t0032g0115others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1569-2516C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214755071 | ||||||
| chr2:214755088
|
C | A | 37 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(34): Show | 39 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1569-2533G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214755088 | ||||||
| chr2:214755136
|
A | G | 4 | a0005c0006t0046g0035a0009c0011t0032g0025a0009c0011t0032g0115others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1569-2581T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214755136 | ||||||
| chr2:214755143
|
A | G | 1 | a0001c0002t0022g0235 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1569-2588T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214755143 | ||||||
| chr2:214755197
|
T | G | 72 | a0001c0002t0004g0017a0001c0002t0004g0019a0001c0002t0004g0285others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1569-2642A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214755197 | ||||||
| chr2:214755294
|
C | T | 275 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(272): Show | 295 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1569-2739G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214755294 | ||||||
| chr2:214755329
|
T | C | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1569-2774A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214755329 | ||||||
| chr2:214755548
|
A | G | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1569-2993T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214755548 | ||||||
| chr2:214755625
|
T | C | 1 | a0004c0007t0058g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1569-3070A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214755625 | ||||||
| chr2:214755725
|
T | C | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1569-3170A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214755725 | ||||||
| chr2:214755801
|
C | T | 173 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(170): Show | 185 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1569-3246G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214755801 | ||||||
| chr2:214755853
|
T | C | 2 | a0002c0001t0001g0147a0002c0001t0001g0175 | 2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1569-3298A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214755853 | ||||||
| chr2:214755897
|
A | G | 3 | a0004c0007t0008g0031a0004c0007t0008g0033a0004c0007t0030g0034 | 3 | HG01069.hp2 HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1569-3342T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214755897 | ||||||
| chr2:214756030
|
T | C | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1569-3475A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756030 | ||||||
| chr2:214756033
|
A | C | 277 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(274): Show | 297 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.1569-3478T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756033 | ||||||
| chr2:214756066
|
A | C | 96 | a0001c0002t0004g0291a0001c0003t0001g0041a0001c0004t0011g0121others(93): Show | 105 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1569-3511T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756066 | ||||||
| chr2:214756070
|
T | C | 1 | a0001c0004t0051g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1569-3515A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756070 | ||||||
| chr2:214756157
|
T | C | 1 | a0002c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1569-3602A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756157 | ||||||
| chr2:214756238
|
G | A | 6 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1569-3683C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756238 | ||||||
| chr2:214756253
|
AG | A | 4 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(1): Show | 4 | HG02257.hp2 HG02273.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1569-3699delC | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756253 | ||||||
| chr2:214756279
|
G | A | 2 | a0002c0001t0009g0139a0019c0026t0025g0331 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1569-3724C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756279 | ||||||
| chr2:214756317
|
A | C | 3 | a0004c0007t0058g0263a0008c0009t0025g0266a0008c0009t0025g0267 | 3 | HG02486.hp1 HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1569-3762T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756317 | ||||||
| chr2:214756398
|
C | T | 168 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(165): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1569-3843G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756398 | ||||||
| chr2:214756442
|
T | C | 1 | a0001c0002t0003g0321 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1569-3887A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756442 | ||||||
| chr2:214756480
|
G | A | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1569-3925C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756480 | ||||||
| chr2:214756655
|
T | G | 168 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(165): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1569-4100A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756655 | ||||||
| chr2:214756747
|
T | A | 105 | a0001c0002t0013g0276a0001c0002t0013g0322a0001c0004t0011g0121others(102): Show | 111 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1569-4192A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756747 | ||||||
| chr2:214756816
|
C | T | 4 | a0002c0001t0001g0168a0005c0006t0020g0022a0005c0006t0020g0023others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1569-4261G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756816 | ||||||
| chr2:214756824
|
A | G | 178 | a0001c0002t0003g0272a0001c0002t0003g0298a0001c0002t0003g0313others(175): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1569-4269T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756824 | ||||||
| chr2:214756867
|
C | T | 336 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(333): Show | 360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.1569-4312G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756867 | ||||||
| chr2:214756971
|
T | A | 152 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(149): Show | 164 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1569-4416A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214756971 | ||||||
| chr2:214757321
|
A | T | 1 | a0005c0006t0001g0036 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1569-4766T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214757321 | ||||||
| chr2:214757506
|
A | T | 154 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(151): Show | 166 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1569-4951T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214757506 | ||||||
| chr2:214757574
|
G | A | 1 | a0002c0033t0001g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1569-5019C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214757574 | ||||||
| chr2:214757606
|
T | C | 51 | a0001c0003t0031g0072a0001c0004t0008g0103a0001c0004t0011g0121others(48): Show | 54 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1569-5051A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214757606 | ||||||
| chr2:214757633
|
TA | T | 5 | a0001c0002t0004g0017a0001c0002t0004g0289a0001c0002t0004g0293others(2): Show | 6 | HG01243.hp1 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1569-5079delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214757633 | ||||||
| chr2:214757721
|
C | A | 7 | a0001c0003t0002g0027a0001c0003t0002g0090a0001c0003t0007g0050others(4): Show | 7 | HG00735.hp1 HG01981.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.1569-5166G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214757721 | ||||||
| chr2:214757827
|
G | T | 1 | a0001c0003t0053g0234 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1569-5272C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214757827 | ||||||
| chr2:214757933
|
C | CA | 127 | a0001c0002t0004g0017a0001c0002t0004g0019a0001c0002t0004g0285others(124): Show | 131 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.1569-5379dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214757933 | ||||||
| chr2:214758017
|
T | C | 50 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(47): Show | 53 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.1569-5462A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214758017 | ||||||
| chr2:214758183
|
C | T | 7 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(4): Show | 8 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1569-5628G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214758183 | ||||||
| chr2:214758217
|
C | A | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1569-5662G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214758217 | ||||||
| chr2:214758227
|
T | C | 68 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(65): Show | 74 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.1569-5672A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214758227 | ||||||
| chr2:214758231
|
C | T | 154 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(151): Show | 166 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1569-5676G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214758231 | ||||||
| chr2:214758255
|
T | C | 1 | a0002c0001t0016g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1569-5700A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214758255 | ||||||
| chr2:214758300
|
G | T | 6 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1569-5745C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214758300 | ||||||
| chr2:214758313
|
A | C | 1 | a0001c0003t0002g0102 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1569-5758T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214758313 | ||||||
| chr2:214758324
|
T | C | 6 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1569-5769A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214758324 | ||||||
| chr2:214758360
|
T | C | 154 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(151): Show | 166 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1569-5805A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214758360 | ||||||
| chr2:214758439
|
C | A | 336 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(333): Show | 360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.1569-5884G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214758439 | ||||||
| chr2:214758666
|
C | T | 157 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(154): Show | 169 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.1569-6111G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214758666 | ||||||
| chr2:214758780
|
T | C | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1569-6225A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214758780 | ||||||
| chr2:214759036
|
G | C | 1 | a0001c0019t0056g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1569-6481C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759036 | ||||||
| chr2:214759080
|
AG | A | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1569-6526delC | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759080 | ||||||
| chr2:214759109
|
T | C | 1 | a0001c0003t0005g0080 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1569-6554A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759109 | ||||||
| chr2:214759285
|
A | G | 2 | a0007c0015t0002g0219a0007c0015t0002g0220 | 2 | HG01074.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1569-6730T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759285 | ||||||
| chr2:214759299
|
T | TA | 4 | a0002c0001t0001g0138a0011c0014t0015g0005a0011c0014t0015g0118others(1): Show | 5 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1569-6745dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759299 | ||||||
| chr2:214759411
|
C | T | 148 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(145): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1569-6856G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759411 | ||||||
| chr2:214759437
|
T | A | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1569-6882A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759437 | ||||||
| chr2:214759543
|
T | A | 4 | a0005c0006t0046g0035a0009c0011t0032g0025a0009c0011t0032g0115others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1569-6988A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759543 | ||||||
| chr2:214759726
|
A | C | 3 | a0001c0004t0018g0277a0001c0004t0018g0280a0001c0004t0018g0281 | 3 | HG02572.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1569-7171T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759726 | ||||||
| chr2:214759764
|
A | G | 2 | a0001c0004t0009g0125a0001c0004t0051g0230 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1569-7209T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759764 | ||||||
| chr2:214759765
|
T | C | 1 | a0004c0007t0068g0265 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1569-7210A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759765 | ||||||
| chr2:214759780
|
T | C | 1 | a0001c0004t0051g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1569-7225A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759780 | ||||||
| chr2:214759818
|
A | T | 150 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(147): Show | 162 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1569-7263T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759818 | ||||||
| chr2:214759955
|
C | T | 150 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(147): Show | 162 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1569-7400G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214759955 | ||||||
| chr2:214760119
|
C | T | 1 | a0012c0013t0052g0226 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1568+7363G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214760119 | ||||||
| chr2:214760151
|
T | G | 2 | a0001c0004t0009g0125a0001c0004t0051g0230 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1568+7331A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214760151 | ||||||
| chr2:214760354
|
G | C | 2 | a0002c0001t0001g0129a0002c0001t0045g0130 | 2 | NA18945.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1568+7128C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214760354 | ||||||
| chr2:214760493
|
C | A | 71 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(68): Show | 71 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1568+6989G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214760493 | ||||||
| chr2:214760717
|
A | G | 1 | a0002c0001t0002g0216 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1568+6765T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214760717 | ||||||
| chr2:214760779
|
C | CT | 92 | a0001c0002t0004g0017a0001c0002t0004g0285a0001c0002t0004g0289others(89): Show | 93 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.1568+6702dupA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214760779 | ||||||
| chr2:214760924
|
A | G | 147 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(144): Show | 159 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1568+6558T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214760924 | ||||||
| chr2:214760936
|
A | G | 48 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(45): Show | 51 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1568+6546T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214760936 | ||||||
| chr2:214760946
|
T | G | 1 | a0001c0002t0003g0335 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1568+6536A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214760946 | ||||||
| chr2:214760986
|
G | A | 148 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(145): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1568+6496C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214760986 | ||||||
| chr2:214760987
|
A | G | 148 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(145): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1568+6495T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214760987 | ||||||
| chr2:214761010
|
G | A | 3 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0021t0022g0236 | 3 | HG01255.hp1 HG01952.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1568+6472C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761010 | ||||||
| chr2:214761011
|
G | T | 148 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(145): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1568+6471C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761011 | ||||||
| chr2:214761021
|
G | A | 148 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(145): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1568+6461C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761021 | ||||||
| chr2:214761025
|
T | C | 248 | a0001c0002t0004g0017a0001c0002t0004g0285a0001c0002t0004g0289others(245): Show | 262 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.1568+6457A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761025 | ||||||
| chr2:214761071
|
T | TA | 146 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(143): Show | 158 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1568+6410dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761071 | ||||||
| chr2:214761129
|
C | A | 336 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(333): Show | 360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.1568+6353G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761129 | ||||||
| chr2:214761251
|
C | T | 148 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(145): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1568+6231G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761251 | ||||||
| chr2:214761289
|
GA | G | 150 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(147): Show | 162 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1568+6192delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761289 | ||||||
| chr2:214761354
|
C | T | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1568+6128G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761354 | ||||||
| chr2:214761374
|
TA | T | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1568+6107delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761374 | ||||||
| chr2:214761402
|
A | T | 1 | a0004c0010t0008g0106 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1568+6080T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761402 | ||||||
| chr2:214761406
|
T | G | 1 | a0004c0010t0008g0106 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1568+6076A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761406 | ||||||
| chr2:214761416
|
A | G | 1 | a0001c0002t0004g0282 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1568+6066T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761416 | ||||||
| chr2:214761463
|
G | A | 148 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(145): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1568+6019C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761463 | ||||||
| chr2:214761515
|
T | G | 1 | a0001c0004t0027g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1568+5967A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761515 | ||||||
| chr2:214761519
|
A | G | 7 | a0008c0009t0021g0015a0008c0009t0021g0223a0008c0009t0049g0222others(4): Show | 9 | HG01109.hp2 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1568+5963T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761519 | ||||||
| chr2:214761627
|
C | T | 29 | a0002c0001t0005g0207a0003c0005t0005g0101a0003c0005t0006g0243others(26): Show | 30 | HG00609.hp2 HG00621.hp2 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.1568+5855G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761627 | ||||||
| chr2:214761643
|
A | T | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1568+5839T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761643 | ||||||
| chr2:214761722
|
A | G | 3 | a0011c0014t0015g0005a0011c0014t0015g0118a0011c0014t0015g0119 | 4 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568+5760T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761722 | ||||||
| chr2:214761736
|
G | C | 1 | a0001c0002t0003g0321 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1568+5746C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761736 | ||||||
| chr2:214761837
|
A | G | 154 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(151): Show | 166 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1568+5645T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761837 | ||||||
| chr2:214761868
|
C | T | 234 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(231): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1568+5614G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761868 | ||||||
| chr2:214761981
|
C | T | 4 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228others(1): Show | 4 | HG02572.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568+5501G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214761981 | ||||||
| chr2:214762097
|
C | T | 6 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568+5385G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762097 | ||||||
| chr2:214762098
|
G | A | 1 | a0001c0002t0003g0329 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1568+5384C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762098 | ||||||
| chr2:214762141
|
G | A | 4 | a0002c0001t0001g0133a0002c0001t0001g0134a0002c0001t0001g0135others(1): Show | 4 | HG01256.hp2 HG01258.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568+5341C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762141 | ||||||
| chr2:214762228
|
T | C | 148 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(145): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1568+5254A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762228 | ||||||
| chr2:214762299
|
C | T | 1 | a0001c0003t0002g0088 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1568+5183G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762299 | ||||||
| chr2:214762384
|
A | C | 148 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(145): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1568+5098T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762384 | ||||||
| chr2:214762503
|
C | A | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1568+4979G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762503 | ||||||
| chr2:214762624
|
C | T | 336 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(333): Show | 360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.1568+4858G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762624 | ||||||
| chr2:214762647
|
T | C | 1 | a0007c0015t0002g0218 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1568+4835A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762647 | ||||||
| chr2:214762656
|
A | C | 148 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(145): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1568+4826T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762656 | ||||||
| chr2:214762673
|
A | G | 148 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(145): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1568+4809T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762673 | ||||||
| chr2:214762754
|
G | A | 3 | a0004c0007t0058g0263a0008c0009t0025g0266a0008c0009t0025g0267 | 3 | HG02486.hp1 HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1568+4728C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762754 | ||||||
| chr2:214762777
|
C | T | 1 | a0007c0015t0002g0218 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1568+4705G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762777 | ||||||
| chr2:214762842
|
T | C | 1 | a0019c0026t0025g0331 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1568+4640A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762842 | ||||||
| chr2:214762888
|
C | A | 148 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(145): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1568+4594G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762888 | ||||||
| chr2:214762890
|
C | G | 6 | a0004c0007t0058g0263a0008c0009t0025g0266a0008c0009t0025g0267others(3): Show | 6 | HG02486.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568+4592G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762890 | ||||||
| chr2:214762924
|
C | G | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1568+4558G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762924 | ||||||
| chr2:214762964
|
C | G | 2 | a0001c0002t0004g0285a0001c0002t0060g0292 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1568+4518G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214762964 | ||||||
| chr2:214763107
|
C | T | 6 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568+4375G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763107 | ||||||
| chr2:214763116
|
C | G | 4 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228others(1): Show | 4 | HG02572.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568+4366G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763116 | ||||||
| chr2:214763131
|
A | C | 2 | a0005c0006t0046g0035a0009c0011t0032g0115 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1568+4351T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763131 | ||||||
| chr2:214763234
|
A | C | 1 | a0001c0002t0003g0272 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1568+4248T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763234 | ||||||
| chr2:214763272
|
T | C | 1 | a0001c0004t0033g0229 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1568+4210A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763272 | ||||||
| chr2:214763275
|
C | T | 148 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(145): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1568+4207G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763275 | ||||||
| chr2:214763303
|
G | A | 3 | a0011c0014t0015g0005a0011c0014t0015g0118a0011c0014t0015g0119 | 4 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568+4179C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763303 | ||||||
| chr2:214763373
|
C | G | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1568+4109G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763373 | ||||||
| chr2:214763389
|
C | A | 1 | a0002c0001t0001g0176 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1568+4093G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763389 | ||||||
| chr2:214763498
|
A | T | 147 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(144): Show | 159 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1568+3984T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763498 | ||||||
| chr2:214763534
|
C | T | 1 | a0001c0019t0056g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1568+3948G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763534 | ||||||
| chr2:214763653
|
A | G | 102 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(99): Show | 112 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1568+3829T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763653 | ||||||
| chr2:214763665
|
C | T | 147 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(144): Show | 159 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1568+3817G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763665 | ||||||
| chr2:214763774
|
T | C | 149 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(146): Show | 161 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1568+3708A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763774 | ||||||
| chr2:214763934
|
A | G | 1 | a0004c0007t0008g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1568+3548T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763934 | ||||||
| chr2:214763937
|
C | A | 147 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(144): Show | 159 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1568+3545G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214763937 | ||||||
| chr2:214764002
|
A | G | 41 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(38): Show | 43 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1568+3480T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764002 | ||||||
| chr2:214764036
|
T | C | 175 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(172): Show | 184 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1568+3446A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764036 | ||||||
| chr2:214764182
|
A | G | 102 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(99): Show | 112 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1568+3300T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764182 | ||||||
| chr2:214764325
|
C | T | 1 | a0003c0005t0041g0026 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1568+3157G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764325 | ||||||
| chr2:214764368
|
C | T | 3 | a0004c0007t0013g0264a0004c0007t0013g0268a0004c0007t0013g0269 | 3 | HG01256.hp1 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1568+3114G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764368 | ||||||
| chr2:214764415
|
C | T | 9 | a0001c0004t0008g0103a0001c0004t0014g0032a0001c0004t0027g0123others(6): Show | 9 | HG00741.hp2 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1568+3067G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764415 | ||||||
| chr2:214764474
|
A | G | 7 | a0008c0009t0021g0015a0008c0009t0021g0223a0008c0009t0049g0222others(4): Show | 9 | HG01109.hp2 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1568+3008T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764474 | ||||||
| chr2:214764475
|
G | C | 1 | a0001c0004t0057g0278 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1568+3007C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764475 | ||||||
| chr2:214764506
|
A | G | 1 | a0002c0001t0002g0216 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1568+2976T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764506 | ||||||
| chr2:214764524
|
A | G | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1568+2958T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764524 | ||||||
| chr2:214764579
|
C | T | 143 | a0001c0002t0007g0056a0001c0004t0008g0103a0001c0004t0011g0121others(140): Show | 155 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1568+2903G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764579 | ||||||
| chr2:214764598
|
A | G | 147 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(144): Show | 155 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1568+2884T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764598 | ||||||
| chr2:214764704
|
C | T | 17 | a0001c0004t0009g0125a0001c0004t0017g0231a0001c0004t0017g0232others(14): Show | 19 | HG01109.hp2 HG01123.hp2 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.1568+2778G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764704 | ||||||
| chr2:214764770
|
A | T | 150 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(147): Show | 163 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1568+2712T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764770 | ||||||
| chr2:214764819
|
G | C | 150 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(147): Show | 163 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1568+2663C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764819 | ||||||
| chr2:214764866
|
A | G | 1 | a0001c0004t0027g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1568+2616T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764866 | ||||||
| chr2:214764957
|
G | GC | 145 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(142): Show | 157 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1568+2524dupG | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214764957 | ||||||
| chr2:214765451
|
C | T | 1 | a0001c0002t0007g0056 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1568+2031G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214765451 | ||||||
| chr2:214765508
|
C | A | 17 | a0001c0004t0009g0125a0001c0004t0017g0231a0001c0004t0017g0232others(14): Show | 19 | HG01109.hp2 HG01123.hp2 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.1568+1974G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214765508 | ||||||
| chr2:214765550
|
G | A | 24 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(21): Show | 27 | HG01109.hp2 HG01123.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1568+1932C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214765550 | ||||||
| chr2:214765648
|
G | T | 337 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(334): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.1568+1834C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214765648 | ||||||
| chr2:214765687
|
C | T | 1 | a0001c0002t0003g0272 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1568+1795G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214765687 | ||||||
| chr2:214765697
|
C | T | 2 | a0008c0009t0025g0266a0008c0009t0025g0267 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1568+1785G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214765697 | ||||||
| chr2:214765750
|
G | A | 2 | a0004c0007t0058g0263a0004c0007t0068g0265 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1568+1732C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214765750 | ||||||
| chr2:214765751
|
T | TAC | 12 | a0002c0001t0001g0001a0002c0001t0001g0151a0002c0001t0001g0177others(9): Show | 16 | HG00438.hp1 HG00741.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1568+1729_1568+173 others(6): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214765751 | ||||||
| chr2:214765751
|
TAC | T | 3 | a0002c0001t0001g0009a0002c0001t0001g0143a0002c0001t0001g0161 | 4 | HG02015.hp1 HG02040.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1568+1729_1568+173 others(6): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214765751 | ||||||
| chr2:214765947
|
T | A | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1568+1535A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214765947 | ||||||
| chr2:214765950
|
G | A | 337 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(334): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.1568+1532C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214765950 | ||||||
| chr2:214766047
|
G | A | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1568+1435C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766047 | ||||||
| chr2:214766236
|
T | C | 155 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(152): Show | 168 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.1568+1246A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766236 | ||||||
| chr2:214766422
|
T | G | 2 | a0001c0004t0009g0125a0001c0004t0051g0230 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1568+1060A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766422 | ||||||
| chr2:214766524
|
T | C | 4 | a0005c0006t0046g0035a0009c0011t0032g0025a0009c0011t0032g0115others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568+958A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766524 | ||||||
| chr2:214766578
|
G | A | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+904C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766578 | ||||||
| chr2:214766583
|
C | T | 1 | a0001c0002t0003g0323 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1568+899G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766583 | ||||||
| chr2:214766619
|
C | CCT | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+862_1568+863i others(4): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766619 | ||||||
| chr2:214766638
|
G | A | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+844C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766638 | ||||||
| chr2:214766677
|
T | C | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1568+805A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766677 | ||||||
| chr2:214766689
|
C | T | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+793G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766689 | ||||||
| chr2:214766700
|
G | A | 5 | a0004c0007t0013g0264a0004c0007t0013g0268a0004c0007t0013g0269others(2): Show | 5 | HG01256.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1568+782C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766700 | ||||||
| chr2:214766743
|
T | A | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+739A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766743 | ||||||
| chr2:214766800
|
G | A | 1 | a0003c0005t0006g0252 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1568+682C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766800 | ||||||
| chr2:214766817
|
C | T | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+665G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766817 | ||||||
| chr2:214766920
|
C | G | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+562G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766920 | ||||||
| chr2:214766928
|
T | A | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+554A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766928 | ||||||
| chr2:214766977
|
T | C | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+505A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766977 | ||||||
| chr2:214766999
|
T | C | 2 | a0001c0004t0009g0125a0001c0004t0051g0230 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1568+483A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214766999 | ||||||
| chr2:214767008
|
T | C | 2 | a0009c0011t0069g0336a0009c0011t0070g0337 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1568+474A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767008 | ||||||
| chr2:214767127
|
C | T | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1568+355G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767127 | ||||||
| chr2:214767132
|
T | C | 1 | a0001c0004t0017g0239 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1568+350A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767132 | ||||||
| chr2:214767208
|
T | C | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+274A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767208 | ||||||
| chr2:214767245
|
T | C | 1 | a0010c0012t0012g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1568+237A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767245 | ||||||
| chr2:214767263
|
A | G | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+219T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767263 | ||||||
| chr2:214767311
|
A | AAGAG | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+170_1568+171i others(6): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767311 | ||||||
| chr2:214767324
|
G | T | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+158C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767324 | ||||||
| chr2:214767371
|
T | G | 25 | a0003c0005t0005g0101a0003c0005t0006g0016a0003c0005t0006g0242others(22): Show | 26 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1568+111A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767371 | ||||||
| chr2:214767396
|
G | T | 7 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(4): Show | 8 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1568+86C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767396 | ||||||
| chr2:214767400
|
ATT | A | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+80_1568+81del others(2): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767400 | ||||||
| chr2:214767401
|
T | C | 39 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(36): Show | 41 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1568+81A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767401 | ||||||
| chr2:214767431
|
T | C | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1568+51A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767431 | ||||||
| chr2:214767440
|
A | G | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1568+42T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767440 | ||||||
| chr2:214767468
|
G | A | 116 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(113): Show | 127 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1568+14C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 6/10 | chr2 | 214767468 | ||||||
| chr2:214767905
|
G | T | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1396-251C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214767905 | ||||||
| chr2:214767933
|
C | G | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1396-279G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214767933 | ||||||
| chr2:214767935
|
A | T | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1396-281T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214767935 | ||||||
| chr2:214767979
|
G | GA | 174 | a0001c0004t0008g0103a0001c0004t0009g0125a0001c0004t0011g0121others(171): Show | 189 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1396-326dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214767979 | ||||||
| chr2:214767992
|
A | G | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1396-338T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214767992 | ||||||
| chr2:214768084
|
T | C | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1396-430A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768084 | ||||||
| chr2:214768186
|
G | C | 7 | a0002c0001t0005g0207a0006c0008t0005g0013a0006c0008t0005g0203others(4): Show | 8 | NA18971.hp2 NA18973.hp1 NA18992.hp1 others(5): Show |
intron_variant | MODIFIER | c.1396-532C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768186 | ||||||
| chr2:214768237
|
C | T | 4 | a0005c0006t0046g0035a0009c0011t0032g0025a0009c0011t0032g0115others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-583G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768237 | ||||||
| chr2:214768267
|
A | C | 117 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(114): Show | 128 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1396-613T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768267 | ||||||
| chr2:214768271
|
A | G | 1 | a0019c0026t0025g0331 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1396-617T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768271 | ||||||
| chr2:214768286
|
T | C | 1 | a0007c0015t0002g0220 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1396-632A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768286 | ||||||
| chr2:214768288
|
CT | C | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1396-635delA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768288 | ||||||
| chr2:214768334
|
C | T | 1 | a0001c0002t0003g0307 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1396-680G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768334 | ||||||
| chr2:214768374
|
C | T | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1396-720G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768374 | ||||||
| chr2:214768438
|
GA | G | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1396-785delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768438 | ||||||
| chr2:214768454
|
A | G | 1 | a0009c0011t0032g0025 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1395+778T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768454 | ||||||
| chr2:214768502
|
C | T | 117 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(114): Show | 128 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1395+730G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768502 | ||||||
| chr2:214768579
|
C | T | 13 | a0002c0001t0001g0164a0002c0001t0001g0165a0002c0001t0001g0166others(10): Show | 14 | HG01346.hp2 HG02080.hp1 NA18949.hp1 others(11): Show |
intron_variant | MODIFIER | c.1395+653G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768579 | ||||||
| chr2:214768582
|
G | GT | 337 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(334): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.1395+649dupA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768582 | ||||||
| chr2:214768643
|
T | C | 7 | a0004c0007t0013g0264a0004c0007t0013g0268a0004c0007t0013g0269others(4): Show | 7 | HG01256.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1395+589A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768643 | ||||||
| chr2:214768668
|
C | T | 1 | a0001c0003t0028g0060 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1395+564G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768668 | ||||||
| chr2:214768687
|
T | C | 117 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(114): Show | 128 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1395+545A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768687 | ||||||
| chr2:214768721
|
C | A | 1 | a0001c0002t0063g0326 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1395+511G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768721 | ||||||
| chr2:214768739
|
A | G | 261 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(258): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1395+493T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768739 | ||||||
| chr2:214768762
|
T | C | 118 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(115): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1395+470A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768762 | ||||||
| chr2:214768773
|
A | C | 2 | a0009c0011t0069g0336a0009c0011t0070g0337 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1395+459T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768773 | ||||||
| chr2:214768799
|
C | T | 1 | a0002c0001t0001g0163 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1395+433G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768799 | ||||||
| chr2:214768900
|
C | T | 69 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(66): Show | 69 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.1395+332G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768900 | ||||||
| chr2:214768925
|
C | T | 2 | a0005c0006t0046g0035a0009c0011t0032g0115 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1395+307G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 5/10 | chr2 | 214768925 | ||||||
| chr2:214769331
|
C | T | 117 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(114): Show | 128 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1315-19G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214769331 | ||||||
| chr2:214769417
|
C | T | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1315-105G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214769417 | ||||||
| chr2:214769463
|
C | T | 2 | a0001c0004t0018g0280a0001c0004t0018g0281 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1315-151G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214769463 | ||||||
| chr2:214769480
|
G | A | 2 | a0001c0003t0001g0041a0001c0003t0040g0052 | 2 | HG03704.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1315-168C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214769480 | ||||||
| chr2:214769508
|
A | G | 261 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(258): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1315-196T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214769508 | ||||||
| chr2:214769512
|
T | C | 261 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(258): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1315-200A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214769512 | ||||||
| chr2:214769514
|
G | A | 56 | a0001c0004t0008g0103a0001c0004t0009g0125a0001c0004t0011g0121others(53): Show | 60 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.1315-202C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214769514 | ||||||
| chr2:214769597
|
C | T | 2 | a0001c0004t0014g0006a0001c0004t0014g0122 | 3 | HG02559.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1315-285G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214769597 | ||||||
| chr2:214769687
|
G | A | 257 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(254): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1315-375C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214769687 | ||||||
| chr2:214769770
|
G | A | 259 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(256): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1315-458C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214769770 | ||||||
| chr2:214769818
|
T | C | 7 | a0008c0009t0021g0015a0008c0009t0021g0223a0008c0009t0049g0222others(4): Show | 9 | HG01109.hp2 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1315-506A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214769818 | ||||||
| chr2:214769903
|
C | T | 121 | a0001c0004t0009g0109a0001c0004t0009g0110a0002c0001t0001g0001others(118): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1315-591G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214769903 | ||||||
| chr2:214769952
|
G | A | 5 | a0001c0003t0002g0097a0001c0003t0002g0099a0001c0003t0002g0102others(2): Show | 5 | HG01123.hp1 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315-640C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214769952 | ||||||
| chr2:214770058
|
T | G | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1315-746A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770058 | ||||||
| chr2:214770111
|
T | C | 130 | a0001c0004t0009g0109a0001c0004t0009g0110a0001c0004t0009g0125others(127): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1315-799A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770111 | ||||||
| chr2:214770154
|
C | CA | 3 | a0011c0014t0015g0005a0011c0014t0015g0118a0011c0014t0015g0119 | 4 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315-843dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770154 | ||||||
| chr2:214770200
|
T | A | 6 | a0001c0004t0009g0004a0001c0004t0009g0111a0001c0004t0009g0112others(3): Show | 7 | HG02109.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1315-888A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770200 | ||||||
| chr2:214770230
|
C | T | 1 | a0002c0001t0005g0207 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1315-918G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770230 | ||||||
| chr2:214770269
|
A | C | 105 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(102): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1315-957T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770269 | ||||||
| chr2:214770281
|
C | T | 1 | a0002c0001t0001g0162 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1315-969G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770281 | ||||||
| chr2:214770375
|
T | C | 5 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1315-1063A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770375 | ||||||
| chr2:214770477
|
C | A | 1 | a0002c0001t0007g0148 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1315-1165G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770477 | ||||||
| chr2:214770497
|
G | A | 47 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(44): Show | 49 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.1315-1185C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770497 | ||||||
| chr2:214770505
|
C | T | 22 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(19): Show | 23 | HG00741.hp2 HG01069.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.1315-1193G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770505 | ||||||
| chr2:214770549
|
C | T | 22 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(19): Show | 23 | HG00741.hp2 HG01069.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.1315-1237G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770549 | ||||||
| chr2:214770564
|
A | T | 4 | a0005c0006t0046g0035a0009c0011t0032g0025a0009c0011t0032g0115others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315-1252T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770564 | ||||||
| chr2:214770759
|
A | G | 1 | a0004c0007t0008g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1315-1447T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770759 | ||||||
| chr2:214770768
|
CGAAGGTA others(6): Show |
C | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1315-1469_1315-145 others(17): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214770768 | ||||||
| chr2:214771070
|
T | C | 60 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(57): Show | 66 | HG00280.hp2 HG00408.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.1315-1758A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771070 | ||||||
| chr2:214771192
|
C | A | 331 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(328): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1315-1880G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771192 | ||||||
| chr2:214771292
|
G | A | 4 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228others(1): Show | 4 | HG02572.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315-1980C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771292 | ||||||
| chr2:214771380
|
T | C | 1 | a0001c0003t0005g0073 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1315-2068A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771380 | ||||||
| chr2:214771392
|
C | T | 1 | a0019c0026t0025g0331 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1315-2080G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771392 | ||||||
| chr2:214771456
|
G | A | 15 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(12): Show | 16 | HG00741.hp2 HG01069.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1315-2144C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771456 | ||||||
| chr2:214771489
|
G | A | 23 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(20): Show | 24 | HG00741.hp2 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1315-2177C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771489 | ||||||
| chr2:214771596
|
T | C | 23 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(20): Show | 24 | HG00741.hp2 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1315-2284A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771596 | ||||||
| chr2:214771597
|
A | G | 23 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(20): Show | 24 | HG00741.hp2 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1315-2285T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771597 | ||||||
| chr2:214771691
|
G | A | 23 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(20): Show | 24 | HG00741.hp2 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1315-2379C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771691 | ||||||
| chr2:214771714
|
C | T | 23 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(20): Show | 24 | HG00741.hp2 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1315-2402G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771714 | ||||||
| chr2:214771729
|
GA | G | 23 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(20): Show | 24 | HG00741.hp2 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1315-2418delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771729 | ||||||
| chr2:214771813
|
G | A | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1315-2501C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771813 | ||||||
| chr2:214771823
|
A | C | 2 | a0001c0003t0002g0040a0001c0003t0002g0078 | 2 | NA19055.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1315-2511T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771823 | ||||||
| chr2:214771924
|
G | GA | 116 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(113): Show | 122 | HG00280.hp2 HG00673.hp1 HG00733.hp1 others(119): Show |
intron_variant | MODIFIER | c.1315-2613dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771924 | ||||||
| chr2:214771924
|
G | GAA | 35 | a0001c0002t0003g0315a0001c0002t0004g0017a0001c0002t0004g0285others(32): Show | 36 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1315-2614_1315-261 others(6): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771924 | ||||||
| chr2:214771924
|
GA | G | 16 | a0002c0001t0001g0161a0004c0007t0008g0031a0004c0007t0008g0033others(13): Show | 18 | HG01069.hp2 HG01175.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1315-2613delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771924 | ||||||
| chr2:214771926
|
A | G | 1 | a0004c0007t0008g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1315-2614T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771926 | ||||||
| chr2:214771927
|
A | G | 1 | a0004c0007t0008g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1315-2615T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771927 | ||||||
| chr2:214771943
|
A | AAAAAAAA others(9): Show |
2 | a0001c0004t0011g0121a0001c0004t0014g0122 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1315-2632_1315-263 others(20): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771943 | ||||||
| chr2:214771943
|
A | AAAAAAAA others(8): Show |
2 | a0001c0004t0014g0006a0001c0004t0027g0124 | 3 | HG03579.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1315-2632_1315-263 others(19): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771943 | ||||||
| chr2:214771943
|
A | AAAAAAAA others(7): Show |
3 | a0001c0004t0008g0103a0001c0004t0014g0032a0001c0004t0027g0123 | 3 | HG00741.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1315-2632_1315-263 others(18): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771943 | ||||||
| chr2:214771960
|
T | C | 15 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(12): Show | 16 | HG00741.hp2 HG01123.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.1315-2648A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771960 | ||||||
| chr2:214771972
|
G | C | 15 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(12): Show | 16 | HG00741.hp2 HG01123.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.1315-2660C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214771972 | ||||||
| chr2:214772127
|
A | G | 84 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(81): Show | 85 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.1315-2815T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772127 | ||||||
| chr2:214772132
|
A | AT | 84 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(81): Show | 85 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.1315-2821dupA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772132 | ||||||
| chr2:214772134
|
T | G | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1315-2822A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772134 | ||||||
| chr2:214772345
|
C | G | 84 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(81): Show | 85 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.1315-3033G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772345 | ||||||
| chr2:214772403
|
C | T | 84 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(81): Show | 85 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.1315-3091G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772403 | ||||||
| chr2:214772421
|
T | C | 84 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(81): Show | 85 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.1315-3109A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772421 | ||||||
| chr2:214772449
|
G | A | 1 | a0009c0011t0032g0025 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1315-3137C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772449 | ||||||
| chr2:214772579
|
T | C | 84 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(81): Show | 85 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.1315-3267A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772579 | ||||||
| chr2:214772595
|
A | G | 141 | a0001c0004t0009g0125a0002c0001t0001g0001a0002c0001t0001g0007others(138): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1315-3283T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772595 | ||||||
| chr2:214772684
|
G | A | 4 | a0001c0003t0002g0092a0001c0003t0010g0091a0007c0015t0002g0219others(1): Show | 4 | HG01074.hp1 HG01109.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1315-3372C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772684 | ||||||
| chr2:214772781
|
G | A | 69 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(66): Show | 76 | HG00280.hp2 HG00408.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.1315-3469C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772781 | ||||||
| chr2:214772871
|
T | G | 84 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(81): Show | 85 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.1315-3559A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772871 | ||||||
| chr2:214772940
|
G | C | 2 | a0001c0003t0002g0057a0001c0003t0002g0058 | 2 | HG02056.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1315-3628C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772940 | ||||||
| chr2:214772945
|
T | C | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1315-3633A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772945 | ||||||
| chr2:214772977
|
A | C | 6 | a0001c0004t0011g0121a0001c0004t0014g0006a0001c0004t0014g0032others(3): Show | 7 | HG02559.hp2 HG02647.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1315-3665T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214772977 | ||||||
| chr2:214773000
|
T | C | 8 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(5): Show | 9 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1315-3688A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773000 | ||||||
| chr2:214773032
|
G | A | 84 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(81): Show | 85 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.1315-3720C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773032 | ||||||
| chr2:214773072
|
C | T | 1 | a0004c0007t0013g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1315-3760G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773072 | ||||||
| chr2:214773089
|
C | G | 15 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(12): Show | 16 | HG00741.hp2 HG01123.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.1315-3777G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773089 | ||||||
| chr2:214773135
|
C | T | 15 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(12): Show | 16 | HG00741.hp2 HG01123.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.1315-3823G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773135 | ||||||
| chr2:214773263
|
A | T | 1 | a0002c0001t0009g0139 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1315-3951T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773263 | ||||||
| chr2:214773273
|
G | A | 17 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(14): Show | 18 | HG00741.hp2 HG01081.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.1315-3961C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773273 | ||||||
| chr2:214773319
|
C | A | 15 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(12): Show | 16 | HG00741.hp2 HG01123.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.1315-4007G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773319 | ||||||
| chr2:214773350
|
A | C | 1 | a0011c0014t0015g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1315-4038T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773350 | ||||||
| chr2:214773476
|
G | T | 1 | a0001c0003t0002g0053 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1315-4164C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773476 | ||||||
| chr2:214773510
|
G | A | 15 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(12): Show | 16 | HG00741.hp2 HG01123.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.1315-4198C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773510 | ||||||
| chr2:214773630
|
GT | G | 15 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(12): Show | 16 | HG00741.hp2 HG01123.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.1315-4319delA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773630 | ||||||
| chr2:214773636
|
T | A | 1 | a0019c0026t0025g0331 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1315-4324A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773636 | ||||||
| chr2:214773636
|
T | TA | 139 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(136): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1315-4325dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773636 | ||||||
| chr2:214773874
|
T | C | 7 | a0004c0007t0013g0264a0004c0007t0013g0268a0004c0007t0013g0269others(4): Show | 7 | HG01256.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1315-4562A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773874 | ||||||
| chr2:214773893
|
C | T | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1315-4581G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773893 | ||||||
| chr2:214773927
|
CTGTTT | C | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1315-4620_1315-461 others(9): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773927 | ||||||
| chr2:214773938
|
A | G | 4 | a0001c0003t0002g0092a0001c0003t0010g0091a0007c0015t0002g0219others(1): Show | 4 | HG01074.hp1 HG01109.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1315-4626T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214773938 | ||||||
| chr2:214774103
|
C | T | 1 | a0001c0004t0051g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1315-4791G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214774103 | ||||||
| chr2:214774202
|
T | C | 25 | a0003c0005t0005g0101a0003c0005t0006g0016a0003c0005t0006g0242others(22): Show | 26 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1315-4890A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214774202 | ||||||
| chr2:214774211
|
T | C | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1315-4899A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214774211 | ||||||
| chr2:214774343
|
C | A | 2 | a0001c0002t0003g0275a0001c0002t0003g0315 | 2 | NA18939.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1315-5031G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214774343 | ||||||
| chr2:214774349
|
C | A | 3 | a0001c0004t0009g0109a0001c0004t0009g0110a0001c0004t0051g0230 | 3 | HG01884.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1315-5037G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214774349 | ||||||
| chr2:214774458
|
A | G | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1315-5146T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214774458 | ||||||
| chr2:214774477
|
G | A | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1315-5165C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214774477 | ||||||
| chr2:214774587
|
C | T | 1 | a0004c0007t0013g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1315-5275G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214774587 | ||||||
| chr2:214774786
|
C | T | 6 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(3): Show | 6 | HG02109.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1315-5474G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214774786 | ||||||
| chr2:214774888
|
T | G | 151 | a0001c0004t0008g0103a0001c0004t0009g0125a0001c0004t0011g0121others(148): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1315-5576A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214774888 | ||||||
| chr2:214774953
|
C | T | 25 | a0003c0005t0005g0101a0003c0005t0006g0016a0003c0005t0006g0242others(22): Show | 26 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1314+5607G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214774953 | ||||||
| chr2:214775070
|
T | A | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+5490A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775070 | ||||||
| chr2:214775085
|
T | C | 5 | a0002c0001t0001g0140a0002c0001t0001g0214a0005c0006t0001g0120others(2): Show | 5 | HG01891.hp2 HG01975.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1314+5475A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775085 | ||||||
| chr2:214775227
|
C | T | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+5333G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775227 | ||||||
| chr2:214775254
|
TA | T | 6 | a0001c0004t0011g0121a0001c0004t0014g0006a0001c0004t0014g0032others(3): Show | 7 | HG02559.hp2 HG02647.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1314+5305delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775254 | ||||||
| chr2:214775297
|
G | A | 3 | a0001c0004t0009g0109a0001c0004t0009g0110a0001c0004t0051g0230 | 3 | HG01884.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1314+5263C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775297 | ||||||
| chr2:214775434
|
A | T | 2 | a0001c0003t0002g0069a0001c0003t0002g0077 | 2 | HG02040.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1314+5126T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775434 | ||||||
| chr2:214775483
|
C | T | 1 | a0005c0006t0066g0333 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1314+5077G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775483 | ||||||
| chr2:214775547
|
T | C | 138 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(135): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1314+5013A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775547 | ||||||
| chr2:214775550
|
T | C | 3 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238 | 3 | HG02257.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1314+5010A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775550 | ||||||
| chr2:214775594
|
T | G | 2 | a0011c0014t0015g0118a0011c0014t0015g0119 | 2 | HG01074.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1314+4966A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775594 | ||||||
| chr2:214775641
|
A | C | 8 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(5): Show | 9 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1314+4919T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775641 | ||||||
| chr2:214775643
|
A | C | 1 | a0002c0001t0001g0128 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1314+4917T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775643 | ||||||
| chr2:214775672
|
T | C | 159 | a0001c0004t0008g0103a0001c0004t0009g0125a0001c0004t0011g0121others(156): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1314+4888A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775672 | ||||||
| chr2:214775799
|
G | A | 1 | a0006c0008t0029g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1314+4761C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214775799 | ||||||
| chr2:214776187
|
G | A | 337 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(334): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.1314+4373C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214776187 | ||||||
| chr2:214776300
|
T | C | 1 | a0019c0026t0025g0331 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1314+4260A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214776300 | ||||||
| chr2:214776388
|
T | C | 79 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(76): Show | 79 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.1314+4172A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214776388 | ||||||
| chr2:214776389
|
G | A | 2 | a0001c0003t0002g0057a0001c0003t0002g0058 | 2 | HG02056.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1314+4171C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214776389 | ||||||
| chr2:214776397
|
T | C | 8 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(5): Show | 9 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1314+4163A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214776397 | ||||||
| chr2:214776411
|
G | A | 7 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(4): Show | 8 | HG00741.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1314+4149C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214776411 | ||||||
| chr2:214776581
|
A | T | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+3979T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214776581 | ||||||
| chr2:214776650
|
G | T | 25 | a0003c0005t0005g0101a0003c0005t0006g0016a0003c0005t0006g0242others(22): Show | 26 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1314+3910C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214776650 | ||||||
| chr2:214776819
|
A | G | 4 | a0001c0004t0014g0006a0001c0004t0014g0122a0009c0011t0069g0336others(1): Show | 5 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1314+3741T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214776819 | ||||||
| chr2:214776931
|
C | G | 138 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(135): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1314+3629G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214776931 | ||||||
| chr2:214777023
|
T | A | 3 | a0004c0007t0013g0264a0004c0007t0013g0268a0004c0007t0013g0269 | 3 | HG01256.hp1 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1314+3537A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214777023 | ||||||
| chr2:214777179
|
A | C | 2 | a0012c0013t0023g0225a0012c0013t0023g0227 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1314+3381T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214777179 | ||||||
| chr2:214777407
|
T | C | 4 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228others(1): Show | 4 | HG02572.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+3153A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214777407 | ||||||
| chr2:214777512
|
T | C | 70 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(67): Show | 70 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.1314+3048A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214777512 | ||||||
| chr2:214777551
|
G | GA | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+3008_1314+300 others(5): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214777551 | ||||||
| chr2:214777615
|
A | T | 2 | a0001c0004t0009g0112a0001c0004t0009g0113 | 2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1314+2945T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214777615 | ||||||
| chr2:214777658
|
T | C | 4 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228others(1): Show | 4 | HG02572.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+2902A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214777658 | ||||||
| chr2:214777999
|
C | G | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1314+2561G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214777999 | ||||||
| chr2:214778024
|
C | T | 1 | a0001c0002t0004g0325 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1314+2536G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778024 | ||||||
| chr2:214778095
|
C | T | 1 | a0001c0003t0002g0068 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1314+2465G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778095 | ||||||
| chr2:214778194
|
C | T | 134 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(131): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1314+2366G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778194 | ||||||
| chr2:214778199
|
C | A | 4 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228others(1): Show | 4 | HG02572.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+2361G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778199 | ||||||
| chr2:214778203
|
T | TC | 57 | a0001c0002t0003g0002a0001c0002t0003g0307a0001c0002t0003g0308others(54): Show | 60 | HG00733.hp1 HG00735.hp1 HG01123.hp1 others(57): Show |
intron_variant | MODIFIER | c.1314+2356dupG | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778203 | ||||||
| chr2:214778216
|
A | C | 138 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(135): Show | 145 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.1314+2344T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778216 | ||||||
| chr2:214778346
|
G | A | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1314+2214C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778346 | ||||||
| chr2:214778571
|
A | G | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+1989T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778571 | ||||||
| chr2:214778657
|
G | A | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+1903C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778657 | ||||||
| chr2:214778755
|
A | C | 1 | a0014c0016t0005g0200 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1314+1805T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778755 | ||||||
| chr2:214778759
|
A | G | 159 | a0001c0004t0008g0103a0001c0004t0009g0125a0001c0004t0011g0121others(156): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1314+1801T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778759 | ||||||
| chr2:214778774
|
A | C | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+1786T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778774 | ||||||
| chr2:214778776
|
C | T | 56 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(53): Show | 62 | HG00280.hp2 HG00408.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.1314+1784G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778776 | ||||||
| chr2:214778816
|
G | A | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1314+1744C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778816 | ||||||
| chr2:214778822
|
T | C | 1 | a0019c0026t0025g0331 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1314+1738A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778822 | ||||||
| chr2:214778987
|
G | A | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+1573C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214778987 | ||||||
| chr2:214779217
|
G | A | 1 | a0001c0004t0009g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1314+1343C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214779217 | ||||||
| chr2:214779287
|
T | C | 1 | a0001c0019t0056g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1314+1273A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214779287 | ||||||
| chr2:214779296
|
G | A | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1314+1264C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214779296 | ||||||
| chr2:214779380
|
C | T | 1 | a0002c0001t0048g0221 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1314+1180G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214779380 | ||||||
| chr2:214779398
|
AT | A | 6 | a0001c0004t0011g0121a0001c0004t0014g0006a0001c0004t0014g0032others(3): Show | 7 | HG02559.hp2 HG02647.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1314+1161delA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214779398 | ||||||
| chr2:214779465
|
A | G | 1 | a0003c0005t0055g0245 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1314+1095T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214779465 | ||||||
| chr2:214779496
|
G | T | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+1064C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214779496 | ||||||
| chr2:214779499
|
T | A | 3 | a0009c0011t0032g0025a0009c0011t0032g0115a0009c0011t0047g0116 | 3 | HG02965.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1314+1061A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214779499 | ||||||
| chr2:214779611
|
C | G | 68 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(65): Show | 75 | HG00280.hp2 HG00408.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.1314+949G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214779611 | ||||||
| chr2:214779612
|
C | G | 1 | a0002c0001t0005g0207 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1314+948G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214779612 | ||||||
| chr2:214779686
|
A | G | 2 | a0003c0005t0006g0273a0003c0005t0006g0274 | 2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1314+874T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214779686 | ||||||
| chr2:214779696
|
C | A | 1 | a0001c0003t0002g0027 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1314+864G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214779696 | ||||||
| chr2:214779760
|
C | T | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1314+800G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214779760 | ||||||
| chr2:214780011
|
G | A | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1314+549C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214780011 | ||||||
| chr2:214780038
|
A | G | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+522T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214780038 | ||||||
| chr2:214780215
|
A | G | 6 | a0001c0004t0011g0121a0001c0004t0014g0006a0001c0004t0014g0032others(3): Show | 7 | HG02559.hp2 HG02647.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1314+345T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214780215 | ||||||
| chr2:214780306
|
T | C | 70 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(67): Show | 70 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.1314+254A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214780306 | ||||||
| chr2:214780322
|
C | T | 225 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(222): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1314+238G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214780322 | ||||||
| chr2:214780374
|
G | A | 2 | a0001c0004t0009g0109a0001c0004t0009g0110 | 2 | HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1314+186C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214780374 | ||||||
| chr2:214780390
|
T | C | 1 | a0002c0001t0038g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1314+170A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214780390 | ||||||
| chr2:214780411
|
A | G | 228 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(225): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1314+149T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214780411 | ||||||
| chr2:214780453
|
GAAAGGTT others(1): Show |
G | 25 | a0003c0005t0005g0101a0003c0005t0006g0016a0003c0005t0006g0242others(22): Show | 26 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1314+99_1314+106de others(9): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214780453 | ||||||
| chr2:214780531
|
G | C | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1314+29C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 4/10 | chr2 | 214780531 | ||||||
| chr2:214781576
|
G | T | 1 | a0001c0002t0003g0286 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.365-67C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214781576 | ||||||
| chr2:214781694
|
C | T | 1 | a0019c0026t0025g0331 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.365-185G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214781694 | ||||||
| chr2:214781959
|
A | G | 70 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(67): Show | 77 | HG00280.hp2 HG00408.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.365-450T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214781959 | ||||||
| chr2:214781965
|
C | G | 2 | a0001c0002t0013g0276a0001c0002t0013g0322 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.365-456G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214781965 | ||||||
| chr2:214782004
|
C | G | 85 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(82): Show | 86 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.365-495G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214782004 | ||||||
| chr2:214782012
|
G | C | 1 | a0001c0002t0003g0260 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.365-503C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214782012 | ||||||
| chr2:214782177
|
G | A | 3 | a0001c0004t0009g0125a0005c0006t0009g0117a0020c0025t0071g0338 | 3 | HG01081.hp2 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.365-668C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214782177 | ||||||
| chr2:214782379
|
C | T | 7 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(4): Show | 8 | HG00741.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.365-870G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214782379 | ||||||
| chr2:214782623
|
A | C | 1 | a0001c0003t0002g0067 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.365-1114T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214782623 | ||||||
| chr2:214782662
|
C | A | 329 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(326): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.365-1153G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214782662 | ||||||
| chr2:214782681
|
A | G | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.365-1172T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214782681 | ||||||
| chr2:214782716
|
T | G | 3 | a0001c0003t0005g0043a0001c0003t0005g0065a0001c0003t0005g0066 | 3 | NA18946.hp2 NA18993.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.365-1207A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214782716 | ||||||
| chr2:214782836
|
G | A | 6 | a0001c0004t0009g0125a0005c0006t0009g0117a0009c0011t0032g0025others(3): Show | 6 | HG01081.hp2 HG02615.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.365-1327C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214782836 | ||||||
| chr2:214782982
|
G | A | 3 | a0009c0011t0032g0025a0009c0011t0032g0115a0009c0011t0047g0116 | 3 | HG02965.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.365-1473C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214782982 | ||||||
| chr2:214783220
|
A | G | 7 | a0004c0007t0008g0031a0004c0007t0008g0033a0004c0007t0008g0037others(4): Show | 7 | HG01069.hp2 HG01175.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.365-1711T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214783220 | ||||||
| chr2:214783264
|
A | T | 3 | a0011c0014t0015g0005a0011c0014t0015g0118a0011c0014t0015g0119 | 4 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.365-1755T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214783264 | ||||||
| chr2:214783270
|
G | A | 329 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(326): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.365-1761C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214783270 | ||||||
| chr2:214783280
|
G | A | 1 | a0002c0001t0048g0221 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.365-1771C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214783280 | ||||||
| chr2:214783293
|
G | A | 1 | a0011c0014t0015g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.365-1784C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214783293 | ||||||
| chr2:214783322
|
G | A | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.365-1813C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214783322 | ||||||
| chr2:214783360
|
C | T | 1 | a0002c0001t0038g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.365-1851G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214783360 | ||||||
| chr2:214783471
|
C | T | 1 | a0001c0003t0040g0052 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.365-1962G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214783471 | ||||||
| chr2:214783531
|
G | A | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.365-2022C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214783531 | ||||||
| chr2:214783649
|
C | T | 1 | a0001c0003t0002g0067 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.365-2140G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214783649 | ||||||
| chr2:214783760
|
C | A | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.365-2251G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214783760 | ||||||
| chr2:214783848
|
C | T | 2 | a0009c0011t0069g0336a0009c0011t0070g0337 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.365-2339G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214783848 | ||||||
| chr2:214783929
|
T | C | 3 | a0009c0011t0032g0025a0009c0011t0032g0115a0009c0011t0047g0116 | 3 | HG02965.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.365-2420A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214783929 | ||||||
| chr2:214784041
|
A | C | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.365-2532T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214784041 | ||||||
| chr2:214784088
|
G | A | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.365-2579C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214784088 | ||||||
| chr2:214784233
|
T | C | 1 | a0001c0004t0009g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.365-2724A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214784233 | ||||||
| chr2:214784261
|
CCAA | C | 55 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(52): Show | 61 | HG00280.hp2 HG00408.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.365-2755_365-2753d others(5): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214784261 | ||||||
| chr2:214784306
|
C | T | 33 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(30): Show | 35 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.365-2797G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214784306 | ||||||
| chr2:214784450
|
A | G | 4 | a0001c0004t0009g0125a0009c0011t0032g0025a0009c0011t0032g0115others(1): Show | 4 | HG02615.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.365-2941T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214784450 | ||||||
| chr2:214784470
|
A | G | 16 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(13): Show | 17 | HG00741.hp2 HG01123.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.365-2961T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214784470 | ||||||
| chr2:214784649
|
T | C | 1 | a0001c0002t0004g0316 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.365-3140A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214784649 | ||||||
| chr2:214784682
|
G | A | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.365-3173C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214784682 | ||||||
| chr2:214784723
|
G | A | 15 | a0004c0007t0008g0031a0004c0007t0008g0033a0004c0007t0008g0037others(12): Show | 17 | HG01069.hp2 HG01109.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.365-3214C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214784723 | ||||||
| chr2:214784731
|
A | T | 7 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(4): Show | 8 | HG00741.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.365-3222T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214784731 | ||||||
| chr2:214784786
|
C | A | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.365-3277G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214784786 | ||||||
| chr2:214784947
|
G | A | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.365-3438C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214784947 | ||||||
| chr2:214785021
|
TA | T | 307 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(304): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.365-3513delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785021 | ||||||
| chr2:214785026
|
AAAAAAAA others(1252): Show |
A | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.365-4776_365-3518d others(2): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785026 | ||||||
| chr2:214785071
|
TTCTTCCC others(6): Show |
T | 139 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(136): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.365-3575_365-3563d others(15): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785071 | ||||||
| chr2:214785090
|
C | T | 4 | a0001c0002t0003g0018a0001c0002t0003g0317a0001c0002t0003g0334others(1): Show | 5 | HG02129.hp2 NA18972.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.365-3581G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785090 | ||||||
| chr2:214785184
|
T | C | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.365-3675A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785184 | ||||||
| chr2:214785200
|
T | C | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.365-3691A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785200 | ||||||
| chr2:214785304
|
T | C | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.365-3795A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785304 | ||||||
| chr2:214785309
|
G | A | 25 | a0003c0005t0005g0101a0003c0005t0006g0016a0003c0005t0006g0242others(22): Show | 26 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.365-3800C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785309 | ||||||
| chr2:214785319
|
C | T | 1 | a0002c0001t0001g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.365-3810G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785319 | ||||||
| chr2:214785441
|
G | T | 2 | a0002c0001t0001g0159a0002c0001t0002g0182 | 2 | HG02135.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.365-3932C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785441 | ||||||
| chr2:214785442
|
C | A | 1 | a0002c0001t0002g0182 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.365-3933G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785442 | ||||||
| chr2:214785504
|
T | G | 2 | a0001c0004t0009g0004a0001c0004t0009g0111 | 3 | HG02109.hp1 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.365-3995A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785504 | ||||||
| chr2:214785511
|
A | G | 4 | a0001c0003t0002g0092a0001c0003t0010g0091a0007c0015t0002g0219others(1): Show | 4 | HG01074.hp1 HG01109.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-4002T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785511 | ||||||
| chr2:214785538
|
T | C | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.365-4029A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785538 | ||||||
| chr2:214785591
|
T | A | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.365-4082A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785591 | ||||||
| chr2:214785658
|
A | G | 1 | a0005c0006t0046g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.365-4149T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785658 | ||||||
| chr2:214785715
|
G | GA | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.365-4207dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785715 | ||||||
| chr2:214785856
|
C | T | 17 | a0001c0004t0008g0103a0001c0004t0009g0125a0001c0004t0011g0121others(14): Show | 18 | HG00741.hp2 HG01081.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.365-4347G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214785856 | ||||||
| chr2:214786152
|
T | C | 2 | a0003c0005t0006g0016a0003c0005t0006g0242 | 3 | HG00735.hp2 HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.365-4643A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214786152 | ||||||
| chr2:214786171
|
G | A | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.365-4662C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214786171 | ||||||
| chr2:214786226
|
T | C | 6 | a0002c0001t0001g0010a0002c0001t0001g0151a0002c0001t0001g0184others(3): Show | 7 | HG00438.hp1 NA18953.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.365-4717A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214786226 | ||||||
| chr2:214786262
|
G | A | 1 | a0002c0001t0001g0191 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.365-4753C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214786262 | ||||||
| chr2:214786285
|
C | G | 2 | a0001c0002t0004g0285a0001c0002t0060g0292 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.365-4776G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214786285 | ||||||
| chr2:214786570
|
CAGGCTTT others(5): Show |
C | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.365-5073_365-5062d others(14): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214786570 | ||||||
| chr2:214786822
|
T | C | 1 | a0001c0003t0002g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.365-5313A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214786822 | ||||||
| chr2:214786834
|
G | A | 2 | a0002c0001t0007g0150a0002c0001t0039g0190 | 2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.365-5325C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214786834 | ||||||
| chr2:214786857
|
C | T | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.365-5348G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214786857 | ||||||
| chr2:214786948
|
T | C | 1 | a0001c0002t0004g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.364+5349A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214786948 | ||||||
| chr2:214787022
|
C | T | 1 | a0001c0004t0009g0112 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.364+5275G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214787022 | ||||||
| chr2:214787026
|
G | A | 56 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(53): Show | 62 | HG00280.hp2 HG00408.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.364+5271C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214787026 | ||||||
| chr2:214787053
|
T | C | 3 | a0002c0001t0002g0014a0002c0001t0002g0216a0002c0001t0002g0217 | 4 | HG00639.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+5244A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214787053 | ||||||
| chr2:214787072
|
T | C | 86 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(83): Show | 87 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.364+5225A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214787072 | ||||||
| chr2:214787080
|
T | A | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.364+5217A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214787080 | ||||||
| chr2:214787118
|
C | T | 1 | a0001c0003t0042g0051 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.364+5179G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214787118 | ||||||
| chr2:214787388
|
T | G | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.364+4909A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214787388 | ||||||
| chr2:214787555
|
G | A | 7 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(4): Show | 8 | HG00741.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.364+4742C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214787555 | ||||||
| chr2:214787694
|
T | C | 4 | a0001c0003t0002g0057a0001c0003t0002g0058a0001c0003t0002g0087others(1): Show | 4 | HG02056.hp1 NA18991.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+4603A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214787694 | ||||||
| chr2:214787699
|
T | G | 329 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(326): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.364+4598A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214787699 | ||||||
| chr2:214787920
|
T | G | 7 | a0004c0007t0013g0264a0004c0007t0013g0268a0004c0007t0013g0269others(4): Show | 7 | HG01256.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.364+4377A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214787920 | ||||||
| chr2:214787997
|
C | T | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.364+4300G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214787997 | ||||||
| chr2:214788075
|
A | T | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.364+4222T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214788075 | ||||||
| chr2:214788107
|
G | A | 4 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(1): Show | 4 | HG02257.hp2 HG02273.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.364+4190C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214788107 | ||||||
| chr2:214788152
|
G | C | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.364+4145C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214788152 | ||||||
| chr2:214788186
|
A | AT | 137 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(134): Show | 144 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.364+4110dupA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214788186 | ||||||
| chr2:214788186
|
AT | A | 7 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(4): Show | 8 | HG00741.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.364+4110delA | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214788186 | ||||||
| chr2:214788254
|
T | G | 1 | a0001c0002t0003g0260 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.364+4043A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214788254 | ||||||
| chr2:214788305
|
T | C | 1 | a0001c0003t0001g0041 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.364+3992A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214788305 | ||||||
| chr2:214788547
|
A | G | 7 | a0001c0003t0005g0043a0001c0003t0005g0064a0001c0003t0005g0065others(4): Show | 7 | HG02109.hp2 NA18946.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.364+3750T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214788547 | ||||||
| chr2:214788661
|
CTACACAT others(7): Show |
C | 1 | a0001c0002t0003g0321 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.364+3622_364+3635d others(16): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214788661 | ||||||
| chr2:214788670
|
A | T | 133 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(130): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.364+3627T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214788670 | ||||||
| chr2:214788800
|
A | G | 1 | a0001c0022t0003g0271 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.364+3497T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214788800 | ||||||
| chr2:214788872
|
C | T | 3 | a0002c0001t0002g0014a0002c0001t0002g0216a0002c0001t0002g0217 | 4 | HG00639.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+3425G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214788872 | ||||||
| chr2:214788984
|
A | G | 2 | a0009c0011t0032g0115a0009c0011t0047g0116 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.364+3313T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214788984 | ||||||
| chr2:214789163
|
T | C | 226 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(223): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.364+3134A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789163 | ||||||
| chr2:214789164
|
C | G | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.364+3133G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789164 | ||||||
| chr2:214789178
|
A | G | 1 | a0014c0016t0005g0200 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.364+3119T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789178 | ||||||
| chr2:214789231
|
A | T | 1 | a0001c0019t0056g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.364+3066T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789231 | ||||||
| chr2:214789239
|
T | G | 1 | a0001c0002t0003g0286 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.364+3058A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789239 | ||||||
| chr2:214789375
|
T | TA | 9 | a0001c0002t0004g0327a0001c0004t0017g0231a0001c0004t0017g0232others(6): Show | 9 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.364+2921dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789375 | ||||||
| chr2:214789375
|
TA | T | 6 | a0001c0002t0003g0275a0001c0003t0043g0063a0002c0001t0001g0129others(3): Show | 7 | HG02735.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.364+2921delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789375 | ||||||
| chr2:214789376
|
A | T | 2 | a0001c0003t0001g0041a0001c0003t0040g0052 | 2 | HG03704.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.364+2921T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789376 | ||||||
| chr2:214789428
|
G | A | 1 | a0001c0004t0018g0279 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.364+2869C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789428 | ||||||
| chr2:214789578
|
G | T | 128 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(125): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.364+2719C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789578 | ||||||
| chr2:214789689
|
G | T | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.364+2608C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789689 | ||||||
| chr2:214789812
|
G | C | 1 | a0005c0006t0020g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.364+2485C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789812 | ||||||
| chr2:214789851
|
G | A | 3 | a0011c0014t0015g0005a0011c0014t0015g0118a0011c0014t0015g0119 | 4 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.364+2446C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789851 | ||||||
| chr2:214789870
|
A | G | 1 | a0001c0002t0004g0291 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.364+2427T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789870 | ||||||
| chr2:214789880
|
T | C | 2 | a0004c0010t0008g0003a0013c0017t0002g0141 | 3 | HG01257.hp2 HG01258.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.364+2417A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214789880 | ||||||
| chr2:214790141
|
A | G | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.364+2156T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214790141 | ||||||
| chr2:214790259
|
C | A | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.364+2038G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214790259 | ||||||
| chr2:214790299
|
C | G | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.364+1998G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214790299 | ||||||
| chr2:214790451
|
A | G | 1 | a0001c0002t0019g0290 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.364+1846T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214790451 | ||||||
| chr2:214790480
|
A | C | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.364+1817T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214790480 | ||||||
| chr2:214790563
|
C | T | 155 | a0001c0004t0008g0103a0001c0004t0009g0125a0001c0004t0011g0121others(152): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.364+1734G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214790563 | ||||||
| chr2:214790650
|
T | C | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.364+1647A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214790650 | ||||||
| chr2:214790660
|
T | C | 5 | a0001c0002t0004g0021a0001c0002t0004g0325a0001c0002t0004g0327others(2): Show | 6 | NA18945.hp2 NA18951.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.364+1637A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214790660 | ||||||
| chr2:214790815
|
A | G | 2 | a0008c0009t0025g0266a0008c0009t0025g0267 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.364+1482T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214790815 | ||||||
| chr2:214790944
|
G | C | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.364+1353C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214790944 | ||||||
| chr2:214791130
|
AAAGT | A | 3 | a0001c0004t0009g0004a0001c0004t0009g0111a0001c0019t0056g0330 | 4 | HG02109.hp1 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+1163_364+1166d others(6): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791130 | ||||||
| chr2:214791161
|
T | C | 1 | a0019c0026t0025g0331 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.364+1136A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791161 | ||||||
| chr2:214791195
|
C | T | 73 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(70): Show | 74 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.364+1102G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791195 | ||||||
| chr2:214791200
|
A | G | 13 | a0004c0007t0008g0031a0004c0007t0008g0033a0004c0007t0030g0034others(10): Show | 15 | HG01069.hp2 HG01109.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.364+1097T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791200 | ||||||
| chr2:214791251
|
T | C | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.364+1046A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791251 | ||||||
| chr2:214791411
|
C | G | 1 | a0003c0005t0006g0244 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.364+886G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791411 | ||||||
| chr2:214791444
|
C | G | 224 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(221): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.364+853G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791444 | ||||||
| chr2:214791470
|
T | C | 1 | a0001c0004t0009g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.364+827A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791470 | ||||||
| chr2:214791521
|
A | G | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.364+776T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791521 | ||||||
| chr2:214791536
|
T | C | 220 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(217): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.364+761A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791536 | ||||||
| chr2:214791840
|
A | G | 1 | a0001c0004t0057g0278 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.364+457T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791840 | ||||||
| chr2:214791922
|
G | A | 3 | a0009c0011t0069g0336a0009c0011t0070g0337a0015c0028t0067g0241 | 3 | HG02109.hp2 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.364+375C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791922 | ||||||
| chr2:214791939
|
T | C | 1 | a0007c0015t0002g0220 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.364+358A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791939 | ||||||
| chr2:214791943
|
A | G | 25 | a0003c0005t0005g0101a0003c0005t0006g0016a0003c0005t0006g0242others(22): Show | 26 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.364+354T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214791943 | ||||||
| chr2:214792150
|
T | TA | 11 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(8): Show | 12 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.364+146dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214792150 | ||||||
| chr2:214792150
|
T | TAA | 10 | a0001c0004t0009g0112a0001c0004t0017g0231a0001c0004t0017g0232others(7): Show | 10 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.364+145_364+146dup others(2): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214792150 | ||||||
| chr2:214792150
|
TA | T | 10 | a0001c0003t0002g0059a0001c0003t0002g0061a0001c0003t0028g0060others(7): Show | 10 | HG01074.hp2 HG01081.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.364+146delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214792150 | ||||||
| chr2:214792194
|
C | G | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.364+103G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214792194 | ||||||
| chr2:214792195
|
G | A | 1 | a0001c0003t0002g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.364+102C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 3/10 | chr2 | 214792195 | ||||||
| chr2:214792458
|
TA | T | 109 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(106): Show | 119 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.216-14delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792458 | ||||||
| chr2:214792458
|
TAA | T | 9 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(6): Show | 9 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.216-15_216-14delTT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792458 | ||||||
| chr2:214792482
|
A | G | 2 | a0002c0001t0001g0008a0002c0001t0001g0213 | 3 | HG03239.hp1 HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.216-37T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792482 | ||||||
| chr2:214792507
|
C | T | 3 | a0004c0007t0008g0031a0004c0007t0008g0033a0004c0007t0030g0034 | 3 | HG01069.hp2 HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.216-62G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792507 | ||||||
| chr2:214792651
|
C | T | 2 | a0001c0003t0002g0057a0001c0003t0002g0058 | 2 | HG02056.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.216-206G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792651 | ||||||
| chr2:214792750
|
T | C | 1 | a0001c0002t0003g0312 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.216-305A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792750 | ||||||
| chr2:214792761
|
C | T | 72 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(69): Show | 73 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.216-316G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792761 | ||||||
| chr2:214792769
|
C | T | 1 | a0001c0002t0003g0283 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.216-324G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792769 | ||||||
| chr2:214792781
|
A | G | 8 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(5): Show | 9 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.216-336T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792781 | ||||||
| chr2:214792783
|
C | G | 2 | a0002c0001t0026g0157a0002c0001t0026g0158 | 2 | NA18991.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.216-338G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792783 | ||||||
| chr2:214792830
|
G | T | 3 | a0001c0003t0002g0090a0001c0003t0007g0050a0001c0003t0007g0089 | 3 | NA18955.hp2 NA18977.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.216-385C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792830 | ||||||
| chr2:214792833
|
C | G | 1 | a0009c0011t0032g0025 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.216-388G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792833 | ||||||
| chr2:214792836
|
C | T | 228 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(225): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.216-391G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792836 | ||||||
| chr2:214792933
|
T | C | 1 | a0007c0015t0002g0220 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.216-488A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792933 | ||||||
| chr2:214792971
|
A | G | 76 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(73): Show | 77 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.216-526T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214792971 | ||||||
| chr2:214793036
|
T | C | 2 | a0001c0002t0003g0313a0001c0002t0003g0314 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.216-591A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214793036 | ||||||
| chr2:214793192
|
C | A | 1 | a0001c0004t0057g0278 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.216-747G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214793192 | ||||||
| chr2:214793300
|
C | T | 1 | a0014c0016t0005g0200 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.216-855G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214793300 | ||||||
| chr2:214793400
|
C | G | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.216-955G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214793400 | ||||||
| chr2:214793443
|
T | G | 1 | a0004c0007t0013g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.216-998A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214793443 | ||||||
| chr2:214793530
|
T | C | 68 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(65): Show | 68 | HG00438.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.216-1085A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214793530 | ||||||
| chr2:214793560
|
T | C | 1 | a0002c0001t0001g0198 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.216-1115A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214793560 | ||||||
| chr2:214793610
|
C | A | 8 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(5): Show | 8 | HG01123.hp2 HG02004.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.216-1165G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214793610 | ||||||
| chr2:214793659
|
G | A | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.216-1214C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214793659 | ||||||
| chr2:214793806
|
A | G | 7 | a0006c0008t0001g0206a0006c0008t0005g0013a0006c0008t0005g0203others(4): Show | 8 | NA18973.hp1 NA18992.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.216-1361T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214793806 | ||||||
| chr2:214793914
|
A | G | 68 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(65): Show | 75 | HG00280.hp2 HG00408.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.216-1469T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214793914 | ||||||
| chr2:214793981
|
G | A | 1 | a0001c0004t0014g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.216-1536C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214793981 | ||||||
| chr2:214794017
|
C | T | 1 | a0001c0002t0003g0320 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.216-1572G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794017 | ||||||
| chr2:214794123
|
T | C | 228 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(225): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.216-1678A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794123 | ||||||
| chr2:214794171
|
A | G | 228 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(225): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.216-1726T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794171 | ||||||
| chr2:214794193
|
G | T | 1 | a0019c0026t0025g0331 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.216-1748C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794193 | ||||||
| chr2:214794238
|
G | A | 1 | a0001c0002t0007g0056 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.216-1793C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794238 | ||||||
| chr2:214794297
|
G | C | 6 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(3): Show | 6 | HG02257.hp2 HG02273.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-1852C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794297 | ||||||
| chr2:214794324
|
C | T | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.216-1879G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794324 | ||||||
| chr2:214794365
|
A | G | 2 | a0001c0002t0003g0287a0001c0002t0059g0318 | 2 | HG02165.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.216-1920T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794365 | ||||||
| chr2:214794585
|
A | ATTC | 226 | a0001c0003t0001g0041a0001c0003t0002g0027a0001c0003t0002g0028others(223): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.216-2141_216-2140i others(5): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794585 | ||||||
| chr2:214794597
|
A | G | 5 | a0001c0002t0004g0021a0001c0002t0004g0325a0001c0002t0004g0327others(2): Show | 6 | NA18945.hp2 NA18951.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-2152T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794597 | ||||||
| chr2:214794613
|
G | A | 3 | a0011c0014t0015g0005a0011c0014t0015g0118a0011c0014t0015g0119 | 4 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-2168C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794613 | ||||||
| chr2:214794628
|
A | G | 1 | a0004c0007t0036g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.216-2183T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794628 | ||||||
| chr2:214794665
|
G | A | 3 | a0002c0001t0001g0188a0002c0001t0001g0189a0002c0001t0016g0011 | 4 | HG01069.hp1 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-2220C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794665 | ||||||
| chr2:214794730
|
C | T | 77 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(74): Show | 85 | HG00280.hp2 HG00408.hp1 HG00673.hp1 others(82): Show |
intron_variant | MODIFIER | c.216-2285G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794730 | ||||||
| chr2:214794804
|
A | G | 1 | a0001c0002t0062g0328 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.215+2257T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794804 | ||||||
| chr2:214794809
|
T | C | 3 | a0011c0014t0015g0005a0011c0014t0015g0118a0011c0014t0015g0119 | 4 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.215+2252A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794809 | ||||||
| chr2:214794884
|
C | T | 139 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0260others(136): Show | 147 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.215+2177G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794884 | ||||||
| chr2:214794990
|
C | T | 1 | a0002c0001t0001g0154 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.215+2071G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214794990 | ||||||
| chr2:214795063
|
G | A | 3 | a0001c0002t0003g0329a0002c0001t0007g0150a0002c0001t0039g0190 | 3 | HG00099.hp1 HG00280.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.215+1998C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795063 | ||||||
| chr2:214795219
|
T | C | 3 | a0004c0010t0008g0105a0004c0010t0008g0106a0004c0010t0030g0104 | 3 | HG00099.hp2 HG01169.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.215+1842A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795219 | ||||||
| chr2:214795398
|
G | A | 2 | a0003c0005t0006g0273a0003c0005t0006g0274 | 2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.215+1663C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795398 | ||||||
| chr2:214795529
|
A | C | 32 | a0001c0003t0002g0114a0003c0005t0006g0016a0003c0005t0006g0242others(29): Show | 33 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.215+1532T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795529 | ||||||
| chr2:214795655
|
G | A | 1 | a0001c0003t0002g0102 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.215+1406C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795655 | ||||||
| chr2:214795727
|
G | A | 10 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(7): Show | 10 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+1334C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795727 | ||||||
| chr2:214795784
|
C | G | 1 | a0003c0005t0055g0245 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.215+1277G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795784 | ||||||
| chr2:214795835
|
C | A | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.215+1226G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795835 | ||||||
| chr2:214795886
|
A | G | 1 | a0001c0003t0002g0053 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.215+1175T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795886 | ||||||
| chr2:214795895
|
G | C | 2 | a0008c0009t0025g0266a0008c0009t0025g0267 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.215+1166C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795895 | ||||||
| chr2:214795896
|
T | C | 1 | a0001c0002t0003g0319 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.215+1165A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795896 | ||||||
| chr2:214795913
|
C | A | 6 | a0001c0004t0011g0121a0001c0004t0014g0006a0001c0004t0014g0122others(3): Show | 7 | HG02559.hp2 HG02647.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+1148G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795913 | ||||||
| chr2:214795919
|
C | A | 13 | a0001c0004t0008g0103a0001c0004t0014g0032a0004c0007t0008g0031others(10): Show | 13 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.215+1142G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795919 | ||||||
| chr2:214795936
|
G | A | 63 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0002g0114others(60): Show | 65 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.215+1125C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795936 | ||||||
| chr2:214795958
|
G | A | 1 | a0017c0027t0002g0085 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.215+1103C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795958 | ||||||
| chr2:214795980
|
C | A | 13 | a0001c0004t0008g0103a0001c0004t0014g0032a0004c0007t0008g0031others(10): Show | 13 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.215+1081G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214795980 | ||||||
| chr2:214796144
|
T | C | 1 | a0019c0026t0025g0331 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.215+917A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214796144 | ||||||
| chr2:214796163
|
A | G | 8 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(5): Show | 9 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.215+898T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214796163 | ||||||
| chr2:214796341
|
A | C | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.215+720T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214796341 | ||||||
| chr2:214796355
|
G | C | 1 | a0001c0003t0031g0086 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.215+706C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214796355 | ||||||
| chr2:214796680
|
T | C | 337 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(334): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.215+381A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214796680 | ||||||
| chr2:214796875
|
T | C | 1 | a0001c0002t0003g0320 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.215+186A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214796875 | ||||||
| chr2:214796929
|
T | C | 11 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(8): Show | 11 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.215+132A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214796929 | ||||||
| chr2:214796956
|
G | C | 32 | a0001c0003t0002g0114a0003c0005t0006g0016a0003c0005t0006g0242others(29): Show | 33 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.215+105C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214796956 | ||||||
| chr2:214796986
|
T | C | 32 | a0001c0003t0002g0114a0003c0005t0006g0016a0003c0005t0006g0242others(29): Show | 33 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.215+75A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214796986 | ||||||
| chr2:214796992
|
CA | C | 11 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(8): Show | 11 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.215+68delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 2/10 | chr2 | 214796992 | ||||||
| chr2:214797159
|
T | G | 1 | a0003c0005t0041g0026 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.159-42A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214797159 | ||||||
| chr2:214797187
|
A | C | 11 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(8): Show | 11 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.159-70T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214797187 | ||||||
| chr2:214797214
|
T | C | 1 | a0005c0006t0034g0262 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159-97A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214797214 | ||||||
| chr2:214797326
|
C | T | 1 | a0003c0005t0006g0273 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.159-209G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214797326 | ||||||
| chr2:214797339
|
G | A | 1 | a0004c0007t0036g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.159-222C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214797339 | ||||||
| chr2:214797355
|
T | C | 1 | a0001c0003t0002g0087 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.159-238A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214797355 | ||||||
| chr2:214797378
|
A | C | 4 | a0001c0003t0001g0041a0001c0003t0002g0049a0001c0003t0002g0088others(1): Show | 4 | HG02015.hp2 HG03688.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-261T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214797378 | ||||||
| chr2:214797653
|
G | A | 5 | a0001c0004t0018g0277a0001c0004t0018g0279a0001c0004t0018g0280others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.159-536C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214797653 | ||||||
| chr2:214797832
|
A | G | 10 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(7): Show | 10 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.159-715T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214797832 | ||||||
| chr2:214797852
|
G | C | 1 | a0002c0001t0001g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.159-735C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214797852 | ||||||
| chr2:214797928
|
A | T | 32 | a0001c0003t0002g0114a0003c0005t0006g0016a0003c0005t0006g0242others(29): Show | 33 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.159-811T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214797928 | ||||||
| chr2:214797954
|
C | A | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.159-837G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214797954 | ||||||
| chr2:214797963
|
A | G | 2 | a0001c0003t0002g0049a0001c0003t0002g0088 | 2 | HG02015.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.159-846T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214797963 | ||||||
| chr2:214798106
|
G | A | 11 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(8): Show | 11 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.159-989C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798106 | ||||||
| chr2:214798143
|
T | C | 1 | a0001c0019t0056g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.159-1026A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798143 | ||||||
| chr2:214798216
|
A | G | 1 | a0009c0011t0070g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.159-1099T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798216 | ||||||
| chr2:214798239
|
TTA | T | 19 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(16): Show | 20 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.159-1124_159-1123d others(4): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798239 | ||||||
| chr2:214798301
|
C | T | 2 | a0002c0001t0001g0133a0002c0001t0001g0134 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.159-1184G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798301 | ||||||
| chr2:214798321
|
T | C | 1 | a0003c0005t0041g0026 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.159-1204A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798321 | ||||||
| chr2:214798495
|
C | A | 6 | a0001c0004t0011g0121a0001c0004t0014g0006a0001c0004t0014g0122others(3): Show | 7 | HG02559.hp2 HG02647.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-1378G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798495 | ||||||
| chr2:214798591
|
T | C | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.159-1474A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798591 | ||||||
| chr2:214798594
|
C | T | 4 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228others(1): Show | 4 | HG02572.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-1477G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798594 | ||||||
| chr2:214798659
|
T | C | 1 | a0005c0006t0034g0262 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159-1542A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798659 | ||||||
| chr2:214798750
|
C | A | 2 | a0001c0004t0009g0112a0001c0004t0009g0113 | 2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.159-1633G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798750 | ||||||
| chr2:214798752
|
A | G | 11 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(8): Show | 11 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.159-1635T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798752 | ||||||
| chr2:214798772
|
GA | G | 306 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(303): Show | 329 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.159-1656delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798772 | ||||||
| chr2:214798772
|
GAA | G | 20 | a0001c0004t0008g0103a0001c0004t0014g0032a0001c0022t0003g0271others(17): Show | 20 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.159-1657_159-1656d others(4): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798772 | ||||||
| chr2:214798772
|
GAAA | G | 6 | a0001c0004t0011g0121a0001c0004t0014g0006a0001c0004t0014g0122others(3): Show | 7 | HG02559.hp2 HG02647.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-1658_159-1656d others(5): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214798772 | ||||||
| chr2:214799083
|
C | T | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.159-1966G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214799083 | ||||||
| chr2:214799249
|
C | T | 8 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(5): Show | 9 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.159-2132G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214799249 | ||||||
| chr2:214799281
|
A | G | 1 | a0005c0006t0009g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.159-2164T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214799281 | ||||||
| chr2:214799376
|
G | A | 8 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(5): Show | 9 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.159-2259C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214799376 | ||||||
| chr2:214799377
|
T | G | 8 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(5): Show | 9 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.159-2260A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214799377 | ||||||
| chr2:214799445
|
T | C | 1 | a0004c0007t0008g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.159-2328A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214799445 | ||||||
| chr2:214799464
|
T | C | 10 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(7): Show | 10 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.159-2347A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214799464 | ||||||
| chr2:214799566
|
C | T | 1 | a0001c0004t0009g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.159-2449G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214799566 | ||||||
| chr2:214799587
|
T | A | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.159-2470A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214799587 | ||||||
| chr2:214799625
|
T | C | 1 | a0002c0001t0001g0191 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.159-2508A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214799625 | ||||||
| chr2:214799667
|
C | T | 62 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0002g0114others(59): Show | 64 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.159-2550G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214799667 | ||||||
| chr2:214799698
|
T | G | 1 | a0002c0001t0001g0192 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.159-2581A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214799698 | ||||||
| chr2:214799811
|
T | A | 1 | a0001c0003t0002g0087 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.159-2694A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214799811 | ||||||
| chr2:214800021
|
T | A | 1 | a0002c0001t0001g0193 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.159-2904A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800021 | ||||||
| chr2:214800091
|
C | T | 1 | a0001c0004t0018g0279 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.159-2974G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800091 | ||||||
| chr2:214800092
|
G | A | 3 | a0007c0015t0002g0195a0007c0030t0044g0153a0007c0032t0002g0194 | 3 | HG01192.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.159-2975C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800092 | ||||||
| chr2:214800183
|
G | C | 5 | a0003c0005t0041g0026a0005c0006t0020g0022a0005c0006t0020g0023others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.159-3066C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800183 | ||||||
| chr2:214800204
|
T | C | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.159-3087A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800204 | ||||||
| chr2:214800251
|
G | A | 2 | a0001c0003t0002g0114a0009c0011t0032g0115 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.159-3134C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800251 | ||||||
| chr2:214800264
|
T | C | 4 | a0012c0013t0023g0225a0012c0013t0023g0227a0012c0013t0023g0228others(1): Show | 4 | HG02572.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-3147A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800264 | ||||||
| chr2:214800265
|
A | G | 1 | a0001c0002t0004g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.159-3148T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800265 | ||||||
| chr2:214800284
|
C | T | 1 | a0001c0002t0003g0288 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.159-3167G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800284 | ||||||
| chr2:214800296
|
G | A | 2 | a0008c0009t0025g0266a0008c0009t0025g0267 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.159-3179C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800296 | ||||||
| chr2:214800497
|
C | T | 1 | a0001c0002t0003g0287 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.159-3380G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800497 | ||||||
| chr2:214800542
|
A | G | 1 | a0006c0008t0005g0209 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.159-3425T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800542 | ||||||
| chr2:214800565
|
T | A | 5 | a0003c0005t0041g0026a0012c0013t0023g0225a0012c0013t0023g0227others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.159-3448A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800565 | ||||||
| chr2:214800671
|
T | C | 2 | a0001c0003t0002g0114a0009c0011t0032g0115 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.159-3554A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800671 | ||||||
| chr2:214800734
|
T | A | 2 | a0001c0003t0002g0049a0001c0003t0002g0088 | 2 | HG02015.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.159-3617A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800734 | ||||||
| chr2:214800770
|
T | A | 1 | a0001c0004t0017g0239 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.159-3653A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800770 | ||||||
| chr2:214800808
|
G | C | 4 | a0001c0004t0017g0231a0001c0004t0017g0232a0001c0004t0017g0238others(1): Show | 4 | HG02257.hp2 HG02273.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-3691C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800808 | ||||||
| chr2:214800900
|
C | T | 8 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(5): Show | 9 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.159-3783G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800900 | ||||||
| chr2:214800982
|
T | A | 3 | a0004c0007t0013g0264a0004c0007t0013g0268a0004c0007t0013g0269 | 3 | HG01256.hp1 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.159-3865A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800982 | ||||||
| chr2:214800998
|
CAT | C | 8 | a0005c0006t0050g0224a0008c0009t0021g0015a0008c0009t0021g0223others(5): Show | 10 | HG01109.hp2 HG02055.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.159-3883_159-3882d others(4): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214800998 | ||||||
| chr2:214801027
|
G | C | 1 | a0001c0002t0003g0321 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.159-3910C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801027 | ||||||
| chr2:214801141
|
G | C | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.159-4024C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801141 | ||||||
| chr2:214801146
|
T | C | 2 | a0002c0001t0001g0196a0002c0001t0001g0197 | 2 | HG00733.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.159-4029A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801146 | ||||||
| chr2:214801167
|
A | G | 2 | a0009c0011t0069g0336a0009c0011t0070g0337 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.159-4050T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801167 | ||||||
| chr2:214801222
|
CAA | C | 11 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(8): Show | 11 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.159-4107_159-4106d others(4): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801222 | ||||||
| chr2:214801517
|
G | A | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.159-4400C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801517 | ||||||
| chr2:214801574
|
T | C | 11 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(8): Show | 11 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.159-4457A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801574 | ||||||
| chr2:214801643
|
T | A | 4 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-4526A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801643 | ||||||
| chr2:214801719
|
A | T | 10 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(7): Show | 10 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.159-4602T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801719 | ||||||
| chr2:214801720
|
T | A | 5 | a0001c0003t0002g0027a0001c0003t0002g0090a0001c0003t0007g0050others(2): Show | 5 | NA18955.hp2 NA18977.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.159-4603A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801720 | ||||||
| chr2:214801802
|
C | T | 1 | a0005c0006t0066g0333 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.159-4685G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801802 | ||||||
| chr2:214801849
|
C | CG | 198 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(195): Show | 215 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.159-4733dupC | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801849 | ||||||
| chr2:214801849
|
C | CGG | 50 | a0001c0002t0003g0275a0001c0002t0003g0283a0001c0002t0003g0286others(47): Show | 51 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.159-4734_159-4733d others(4): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801849 | ||||||
| chr2:214801849
|
CG | C | 38 | a0001c0003t0002g0114a0001c0004t0009g0109a0001c0004t0009g0110others(35): Show | 39 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.159-4733delC | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801849 | ||||||
| chr2:214801849
|
CGG | C | 20 | a0001c0004t0008g0103a0001c0004t0011g0121a0001c0004t0014g0006others(17): Show | 21 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.159-4734_159-4733d others(4): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801849 | ||||||
| chr2:214801851
|
G | GT | 4 | a0002c0001t0001g0007a0002c0001t0001g0138a0002c0001t0001g0140others(1): Show | 5 | HG01975.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.159-4735_159-4734i others(3): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801851 | ||||||
| chr2:214801854
|
G | T | 1 | a0001c0004t0014g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.159-4737C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801854 | ||||||
| chr2:214801878
|
A | G | 337 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(334): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.159-4761T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801878 | ||||||
| chr2:214801887
|
TC | T | 2 | a0003c0005t0006g0016a0003c0005t0006g0242 | 3 | HG00735.hp2 HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.159-4771delG | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801887 | ||||||
| chr2:214801965
|
C | T | 1 | a0004c0007t0008g0031 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.159-4848G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214801965 | ||||||
| chr2:214802065
|
T | G | 4 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-4948A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802065 | ||||||
| chr2:214802088
|
A | G | 2 | a0002c0001t0011g0137a0002c0001t0011g0211 | 2 | HG00408.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.159-4971T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802088 | ||||||
| chr2:214802126
|
T | C | 11 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(8): Show | 11 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.159-5009A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802126 | ||||||
| chr2:214802138
|
C | G | 4 | a0002c0001t0001g0133a0002c0001t0001g0134a0002c0001t0001g0135others(1): Show | 4 | HG01256.hp2 HG01258.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-5021G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802138 | ||||||
| chr2:214802180
|
T | C | 131 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(128): Show | 138 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.159-5063A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802180 | ||||||
| chr2:214802266
|
T | G | 1 | a0006c0008t0005g0209 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.159-5149A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802266 | ||||||
| chr2:214802335
|
A | G | 1 | a0001c0004t0011g0121 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.159-5218T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802335 | ||||||
| chr2:214802359
|
G | A | 1 | a0001c0004t0009g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.159-5242C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802359 | ||||||
| chr2:214802424
|
T | C | 62 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0002g0114others(59): Show | 64 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.159-5307A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802424 | ||||||
| chr2:214802492
|
C | G | 1 | a0001c0002t0004g0282 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.159-5375G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802492 | ||||||
| chr2:214802572
|
ATT | A | 5 | a0003c0005t0041g0026a0005c0006t0020g0022a0005c0006t0020g0023others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.159-5457_159-5456d others(4): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802572 | ||||||
| chr2:214802581
|
G | A | 5 | a0003c0005t0041g0026a0005c0006t0020g0022a0005c0006t0020g0023others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.159-5464C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802581 | ||||||
| chr2:214802636
|
T | C | 26 | a0001c0003t0002g0114a0003c0005t0006g0016a0003c0005t0006g0242others(23): Show | 27 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.159-5519A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802636 | ||||||
| chr2:214802834
|
T | C | 1 | a0003c0005t0041g0026 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.159-5717A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214802834 | ||||||
| chr2:214803013
|
A | G | 1 | a0009c0011t0069g0336 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.159-5896T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803013 | ||||||
| chr2:214803032
|
G | C | 62 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0002g0114others(59): Show | 64 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.159-5915C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803032 | ||||||
| chr2:214803064
|
C | CA | 131 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(128): Show | 138 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.159-5948dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803064 | ||||||
| chr2:214803064
|
C | T | 1 | a0002c0001t0001g0132 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.159-5947G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803064 | ||||||
| chr2:214803098
|
G | A | 7 | a0001c0004t0009g0125a0001c0004t0011g0121a0001c0004t0014g0006others(4): Show | 8 | HG02559.hp2 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.159-5981C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803098 | ||||||
| chr2:214803154
|
C | T | 62 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0002g0114others(59): Show | 64 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.159-6037G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803154 | ||||||
| chr2:214803190
|
A | AGGCCTCA others(1): Show |
62 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0002g0114others(59): Show | 64 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.159-6074_159-6073i others(10): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803190 | ||||||
| chr2:214803264
|
G | A | 62 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0002g0114others(59): Show | 64 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.159-6147C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803264 | ||||||
| chr2:214803270
|
G | A | 1 | a0001c0003t0002g0040 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.158+6142C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803270 | ||||||
| chr2:214803271
|
A | C | 1 | a0001c0003t0002g0040 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.158+6141T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803271 | ||||||
| chr2:214803321
|
G | A | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.158+6091C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803321 | ||||||
| chr2:214803323
|
G | A | 6 | a0001c0004t0011g0121a0001c0004t0014g0006a0001c0004t0014g0122others(3): Show | 7 | HG02559.hp2 HG02647.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+6089C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803323 | ||||||
| chr2:214803378
|
T | A | 1 | a0002c0001t0007g0199 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.158+6034A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803378 | ||||||
| chr2:214803425
|
G | A | 62 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0002g0114others(59): Show | 64 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.158+5987C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803425 | ||||||
| chr2:214803447
|
G | A | 8 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(5): Show | 9 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.158+5965C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803447 | ||||||
| chr2:214803483
|
G | A | 1 | a0003c0005t0006g0256 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.158+5929C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803483 | ||||||
| chr2:214803524
|
C | A | 62 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0002g0114others(59): Show | 64 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.158+5888G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803524 | ||||||
| chr2:214803547
|
C | T | 14 | a0001c0004t0009g0004a0001c0004t0009g0109a0001c0004t0009g0110others(11): Show | 15 | HG01081.hp2 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.158+5865G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803547 | ||||||
| chr2:214803707
|
G | A | 5 | a0001c0002t0004g0021a0001c0002t0004g0325a0001c0002t0004g0327others(2): Show | 6 | NA18945.hp2 NA18951.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+5705C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803707 | ||||||
| chr2:214803770
|
A | C | 62 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0002g0114others(59): Show | 64 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.158+5642T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803770 | ||||||
| chr2:214803799
|
C | T | 2 | a0001c0003t0005g0096a0001c0003t0005g0108 | 2 | NA18978.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.158+5613G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803799 | ||||||
| chr2:214803864
|
T | A | 2 | a0001c0003t0002g0094a0005c0006t0001g0093 | 2 | NA18747.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.158+5548A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803864 | ||||||
| chr2:214803907
|
T | A | 8 | a0005c0006t0050g0224a0008c0009t0021g0015a0008c0009t0021g0223others(5): Show | 10 | HG01109.hp2 HG02055.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.158+5505A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803907 | ||||||
| chr2:214803940
|
C | T | 3 | a0005c0006t0020g0022a0005c0006t0020g0023a0005c0006t0020g0024 | 3 | HG01884.hp2 HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.158+5472G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214803940 | ||||||
| chr2:214804062
|
A | G | 26 | a0001c0003t0002g0114a0003c0005t0006g0016a0003c0005t0006g0242others(23): Show | 27 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.158+5350T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214804062 | ||||||
| chr2:214804143
|
G | A | 1 | a0001c0002t0062g0328 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.158+5269C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214804143 | ||||||
| chr2:214804210
|
CAAGTA | C | 3 | a0002c0001t0001g0129a0002c0001t0045g0130a0006c0008t0029g0210 | 3 | NA18945.hp1 NA19000.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.158+5197_158+5201d others(7): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214804210 | ||||||
| chr2:214804352
|
A | T | 21 | a0003c0005t0006g0016a0003c0005t0006g0242a0003c0005t0006g0243others(18): Show | 22 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.158+5060T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214804352 | ||||||
| chr2:214804423
|
A | G | 6 | a0001c0004t0011g0121a0001c0004t0014g0006a0001c0004t0014g0122others(3): Show | 7 | HG02559.hp2 HG02647.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+4989T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214804423 | ||||||
| chr2:214804654
|
T | C | 1 | a0020c0025t0071g0338 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.158+4758A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214804654 | ||||||
| chr2:214804861
|
T | A | 6 | a0001c0004t0011g0121a0001c0004t0014g0006a0001c0004t0014g0122others(3): Show | 7 | HG02559.hp2 HG02647.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+4551A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214804861 | ||||||
| chr2:214805017
|
C | T | 1 | a0001c0002t0013g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.158+4395G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805017 | ||||||
| chr2:214805018
|
G | A | 3 | a0003c0005t0006g0258a0003c0005t0035g0257a0003c0005t0035g0259 | 3 | HG00621.hp2 NA18951.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.158+4394C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805018 | ||||||
| chr2:214805022
|
T | G | 133 | a0001c0002t0007g0056a0001c0002t0022g0233a0001c0002t0022g0235others(130): Show | 135 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.158+4390A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805022 | ||||||
| chr2:214805031
|
C | T | 1 | a0001c0004t0051g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.158+4381G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805031 | ||||||
| chr2:214805110
|
G | A | 10 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(7): Show | 10 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.158+4302C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805110 | ||||||
| chr2:214805132
|
G | C | 6 | a0001c0004t0011g0121a0001c0004t0014g0006a0001c0004t0014g0122others(3): Show | 7 | HG02559.hp2 HG02647.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+4280C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805132 | ||||||
| chr2:214805156
|
G | A | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158+4256C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805156 | ||||||
| chr2:214805252
|
C | T | 1 | a0001c0002t0003g0275 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.158+4160G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805252 | ||||||
| chr2:214805261
|
C | T | 2 | a0001c0004t0033g0229a0005c0006t0009g0117 | 2 | HG03098.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.158+4151G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805261 | ||||||
| chr2:214805703
|
T | C | 1 | a0001c0004t0009g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.158+3709A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805703 | ||||||
| chr2:214805705
|
T | C | 8 | a0005c0006t0050g0224a0008c0009t0021g0015a0008c0009t0021g0223others(5): Show | 10 | HG01109.hp2 HG02055.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.158+3707A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805705 | ||||||
| chr2:214805767
|
GAA | G | 30 | a0001c0003t0002g0114a0003c0005t0006g0016a0003c0005t0006g0242others(27): Show | 31 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.158+3643_158+3644d others(4): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805767 | ||||||
| chr2:214805837
|
A | T | 30 | a0001c0003t0002g0114a0003c0005t0006g0016a0003c0005t0006g0242others(27): Show | 31 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.158+3575T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805837 | ||||||
| chr2:214805955
|
A | G | 5 | a0009c0011t0047g0116a0012c0013t0023g0225a0012c0013t0023g0227others(2): Show | 5 | HG02572.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+3457T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805955 | ||||||
| chr2:214805960
|
C | T | 28 | a0001c0003t0002g0114a0003c0005t0006g0016a0003c0005t0006g0242others(25): Show | 29 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.158+3452G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805960 | ||||||
| chr2:214805969
|
T | C | 8 | a0002c0001t0001g0208a0002c0001t0005g0207a0006c0008t0001g0206others(5): Show | 9 | NA18971.hp2 NA18973.hp1 NA18992.hp1 others(6): Show |
intron_variant | MODIFIER | c.158+3443A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214805969 | ||||||
| chr2:214806113
|
G | A | 1 | a0001c0002t0003g0329 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.158+3299C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806113 | ||||||
| chr2:214806188
|
G | A | 1 | a0001c0003t0002g0095 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.158+3224C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806188 | ||||||
| chr2:214806305
|
C | T | 1 | a0002c0001t0016g0131 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.158+3107G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806305 | ||||||
| chr2:214806424
|
C | T | 1 | a0001c0003t0002g0028 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.158+2988G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806424 | ||||||
| chr2:214806428
|
A | C | 3 | a0002c0001t0001g0129a0002c0001t0045g0130a0006c0008t0029g0210 | 3 | NA18945.hp1 NA19000.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.158+2984T>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806428 | ||||||
| chr2:214806593
|
A | G | 254 | a0001c0002t0007g0056a0001c0002t0022g0233a0001c0002t0022g0235others(251): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.158+2819T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806593 | ||||||
| chr2:214806648
|
C | T | 233 | a0001c0002t0007g0056a0001c0003t0001g0041a0001c0003t0002g0027others(230): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.158+2764G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806648 | ||||||
| chr2:214806711
|
T | C | 2 | a0001c0003t0005g0096a0001c0003t0005g0108 | 2 | NA18978.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.158+2701A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806711 | ||||||
| chr2:214806752
|
T | C | 105 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(102): Show | 116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.158+2660A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806752 | ||||||
| chr2:214806779
|
C | G | 6 | a0001c0004t0011g0121a0001c0004t0014g0006a0001c0004t0014g0122others(3): Show | 7 | HG02559.hp2 HG02647.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+2633G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806779 | ||||||
| chr2:214806790
|
C | T | 3 | a0001c0002t0003g0272a0001c0002t0024g0270a0001c0022t0003g0271 | 3 | HG01175.hp2 HG01516.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.158+2622G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806790 | ||||||
| chr2:214806810
|
G | A | 7 | a0001c0003t0002g0097a0001c0003t0002g0099a0001c0003t0002g0102others(4): Show | 8 | HG01123.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.158+2602C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806810 | ||||||
| chr2:214806857
|
G | A | 4 | a0001c0004t0008g0103a0004c0010t0008g0105a0004c0010t0008g0106others(1): Show | 4 | HG00099.hp2 HG00741.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+2555C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806857 | ||||||
| chr2:214806874
|
G | GAAA | 16 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(13): Show | 16 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.158+2537_158+2538i others(5): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806874 | ||||||
| chr2:214806875
|
G | A | 16 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(13): Show | 16 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.158+2537C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806875 | ||||||
| chr2:214806875
|
G | GA | 82 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(79): Show | 91 | HG00280.hp2 HG00408.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.158+2536_158+2537i others(3): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806875 | ||||||
| chr2:214806875
|
G | GAA | 32 | a0001c0003t0002g0114a0001c0004t0009g0004a0001c0004t0009g0111others(29): Show | 35 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.158+2536_158+2537i others(4): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806875 | ||||||
| chr2:214806875
|
G | GAAA | 89 | a0001c0002t0007g0056a0001c0003t0001g0041a0001c0003t0002g0027others(86): Show | 90 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.158+2536_158+2537i others(5): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806875 | ||||||
| chr2:214806875
|
G | GAAAA | 4 | a0001c0003t0002g0107a0001c0003t0005g0108a0009c0011t0069g0336others(1): Show | 4 | HG02486.hp2 HG02922.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+2536_158+2537i others(6): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806875 | ||||||
| chr2:214806876
|
G | A | 232 | a0001c0002t0003g0002a0001c0002t0003g0018a0001c0002t0003g0020others(229): Show | 245 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.158+2536C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806876 | ||||||
| chr2:214806876
|
G | GAAA | 99 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(96): Show | 110 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.158+2533_158+2535d others(5): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806876 | ||||||
| chr2:214806876
|
G | GAAAA | 6 | a0002c0001t0001g0212a0002c0001t0001g0213a0002c0001t0001g0214others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+2532_158+2535d others(6): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806876 | ||||||
| chr2:214806897
|
C | G | 16 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(13): Show | 16 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.158+2515G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214806897 | ||||||
| chr2:214807014
|
T | C | 16 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(13): Show | 16 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.158+2398A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214807014 | ||||||
| chr2:214807161
|
A | G | 16 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(13): Show | 16 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.158+2251T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214807161 | ||||||
| chr2:214807190
|
T | A | 5 | a0003c0005t0041g0026a0005c0006t0020g0022a0005c0006t0020g0023others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+2222A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214807190 | ||||||
| chr2:214807215
|
TA | T | 23 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0002g0027others(20): Show | 24 | HG01255.hp1 HG01884.hp1 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.158+2196delT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214807215 | ||||||
| chr2:214807317
|
T | C | 16 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(13): Show | 16 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.158+2095A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214807317 | ||||||
| chr2:214807537
|
T | C | 3 | a0002c0001t0002g0014a0002c0001t0002g0216a0002c0001t0002g0217 | 4 | HG00639.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+1875A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214807537 | ||||||
| chr2:214807623
|
C | T | 105 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(102): Show | 116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.158+1789G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214807623 | ||||||
| chr2:214807677
|
T | C | 15 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(12): Show | 15 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.158+1735A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214807677 | ||||||
| chr2:214807718
|
A | G | 5 | a0003c0005t0041g0026a0005c0006t0020g0022a0005c0006t0020g0023others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+1694T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214807718 | ||||||
| chr2:214807737
|
T | TGAGGCTC others(1): Show |
252 | a0001c0002t0007g0056a0001c0002t0022g0233a0001c0002t0022g0235others(249): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.158+1674_158+1675i others(10): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214807737 | ||||||
| chr2:214807803
|
C | T | 15 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(12): Show | 15 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.158+1609G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214807803 | ||||||
| chr2:214807822
|
G | T | 252 | a0001c0002t0007g0056a0001c0002t0022g0233a0001c0002t0022g0235others(249): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.158+1590C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214807822 | ||||||
| chr2:214808069
|
G | C | 192 | a0001c0002t0007g0056a0001c0003t0001g0041a0001c0003t0002g0027others(189): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.158+1343C>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808069 | ||||||
| chr2:214808076
|
T | C | 15 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(12): Show | 15 | HG01255.hp1 HG01952.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.158+1336A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808076 | ||||||
| chr2:214808103
|
C | T | 192 | a0001c0002t0007g0056a0001c0003t0001g0041a0001c0003t0002g0027others(189): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.158+1309G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808103 | ||||||
| chr2:214808109
|
A | G | 87 | a0001c0002t0007g0056a0001c0003t0001g0041a0001c0003t0002g0027others(84): Show | 88 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.158+1303T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808109 | ||||||
| chr2:214808189
|
C | T | 1 | a0002c0001t0001g0128 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.158+1223G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808189 | ||||||
| chr2:214808238
|
T | A | 1 | a0001c0002t0003g0332 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.158+1174A>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808238 | ||||||
| chr2:214808273
|
A | G | 20 | a0001c0002t0003g0260a0003c0005t0006g0016a0003c0005t0006g0242others(17): Show | 21 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.158+1139T>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808273 | ||||||
| chr2:214808345
|
C | T | 105 | a0002c0001t0001g0001a0002c0001t0001g0007a0002c0001t0001g0008others(102): Show | 116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.158+1067G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808345 | ||||||
| chr2:214808374
|
A | T | 14 | a0001c0003t0002g0114a0001c0004t0009g0004a0001c0004t0009g0109others(11): Show | 16 | HG01074.hp2 HG01081.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.158+1038T>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808374 | ||||||
| chr2:214808387
|
C | T | 1 | a0005c0006t0001g0120 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.158+1025G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808387 | ||||||
| chr2:214808494
|
G | GA | 233 | a0001c0002t0007g0056a0001c0002t0022g0233a0001c0002t0022g0235others(230): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.158+917dupT | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808494 | ||||||
| chr2:214808578
|
C | G | 6 | a0001c0004t0011g0121a0001c0004t0014g0006a0001c0004t0014g0122others(3): Show | 7 | HG02559.hp2 HG02647.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+834G>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808578 | ||||||
| chr2:214808659
|
C | T | 1 | a0015c0028t0067g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158+753G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808659 | ||||||
| chr2:214808700
|
CAAG | C | 200 | a0001c0002t0007g0056a0001c0003t0001g0041a0001c0003t0002g0027others(197): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.158+709_158+711del others(3): Show |
BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808700 | ||||||
| chr2:214808716
|
T | C | 232 | a0001c0002t0007g0056a0001c0002t0022g0233a0001c0002t0022g0235others(229): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.158+696A>G | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808716 | ||||||
| chr2:214808940
|
C | T | 190 | a0001c0002t0007g0056a0001c0003t0001g0041a0001c0003t0002g0027others(187): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.158+472G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214808940 | ||||||
| chr2:214809015
|
T | G | 234 | a0001c0002t0007g0056a0001c0002t0022g0233a0001c0002t0022g0235others(231): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.158+397A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214809015 | ||||||
| chr2:214809069
|
G | T | 19 | a0001c0002t0022g0233a0001c0002t0022g0235a0001c0003t0053g0234others(16): Show | 20 | HG01109.hp2 HG01255.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.158+343C>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214809069 | ||||||
| chr2:214809072
|
G | A | 1 | a0004c0007t0008g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.158+340C>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214809072 | ||||||
| chr2:214809073
|
C | T | 5 | a0003c0005t0041g0026a0005c0006t0020g0022a0005c0006t0020g0023others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+339G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214809073 | ||||||
| chr2:214809213
|
C | T | 237 | a0001c0002t0003g0334a0001c0002t0003g0335a0001c0002t0007g0056others(234): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.158+199G>A | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214809213 | ||||||
| chr2:214809224
|
C | A | 2 | a0007c0015t0002g0219a0007c0015t0002g0220 | 2 | HG01074.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.158+188G>T | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214809224 | ||||||
| chr2:214809366
|
T | G | 238 | a0001c0002t0003g0334a0001c0002t0003g0335a0001c0002t0007g0056others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.158+46A>C | BARD1 | ENSG00000138376.11 | transcript | ENST00000260947.9 | protein_coding | 1/10 | chr2 | 214809366 |