Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8927 |
|---|---|
| ensemblid | ENSG00000164061.5 |
| hgncid | 1117 |
| symbol | BSN |
| name | bassoon presynaptic cytomatrix protein |
| refseq_nuc | NM_003458.4 |
| refseq_prot | NP_003449.2 |
| ensembl_nuc | ENST00000296452.5 |
| ensembl_prot | ENSP00000296452.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 49554477 |
| end | 49671549 |
| strand | + |
| ver | v1.2 |
| region | chr3:49554477-49671549 |
| region5000 | chr3:49549477-49676549 |
| regionname0 | BSN_chr3_49554477_49671549 |
| regionname5000 | BSN_chr3_49549477_49676549 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 3926 | 69 | 23 | 17 | 15 | 3 | 10 | 13 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002 | 0/0 | 3926 | 46 | 13 | 14 | 6 | 7 | 6 | 5 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003 | 1/0 | 3926 | 31 | 21 | 5 | 0 | 3 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0004 | 0/0 | 3926 | 5 | 1 | 3 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0005 | 0/0 | 3926 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0006 | 0/0 | 3926 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0007 | 0/0 | 3926 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0008 | 0/0 | 3926 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0009 | 0/0 | 3926 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0010 | 0/0 | 3926 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0011 | 0/0 | 3926 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0012 | 0/0 | 3926 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0013 | 0/0 | 3926 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0014 | 0/0 | 3926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0015 | 0/0 | 3926 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0016 | 0/0 | 3926 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0017 | 0/0 | 3926 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0018 | 0/0 | 3926 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0019 | 0/0 | 3926 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0020 | 0/0 | 3926 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0021 | 0/0 | 3926 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0022 | 0/0 | 3926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0023 | 0/0 | 3926 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0024 | 0/0 | 3926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0025 | 0/0 | 3926 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 11781 | 66 | 23 | 16 | 13 | 3 | 10 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0002 | 0/0 | 11781 | 41 | 11 | 12 | 6 | 6 | 6 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0003 | 0/0 | 11781 | 15 | 14 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0004 | 1/0 | 11781 | 14 | 6 | 3 | 0 | 3 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0005 | 0/0 | 11781 | 4 | 0 | 0 | 4 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0006 | 0/0 | 11781 | 4 | 1 | 2 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0007 | 0/0 | 11781 | 3 | 3 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0008 | 0/0 | 11781 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0009 | 0/0 | 11781 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0010 | 0/0 | 11781 | 2 | 0 | 0 | 2 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0011 | 0/0 | 11781 | 2 | 0 | 0 | 1 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0012 | 0/0 | 11781 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0013 | 0/0 | 11781 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0014 | 0/0 | 11781 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0015 | 0/0 | 11781 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0016 | 0/0 | 11781 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0017 | 0/0 | 11781 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0018 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0019 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0020 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0021 | 0/0 | 11781 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0022 | 0/0 | 11781 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0023 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0024 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0025 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0026 | 0/0 | 11781 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0027 | 0/0 | 11781 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0028 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0029 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0030 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0031 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0032 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0033 | 0/0 | 11781 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0034 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0035 | 0/0 | 11781 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0036 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0037 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| c0038 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4189 | 46 | 14 | 11 | 7 | 8 | 6 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0002 | 0/0 | 4189 | 38 | 8 | 9 | 12 | 2 | 7 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0003 | 0/1 | 4189 | 25 | 15 | 5 | 1 | 0 | 3 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0004 | 0/0 | 4191 | 18 | 13 | 5 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0005 | 0/0 | 4189 | 6 | 0 | 5 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0006 | 0/0 | 4191 | 6 | 2 | 0 | 0 | 3 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0007 | 0/0 | 4189 | 6 | 6 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0008 | 0/0 | 4189 | 4 | 0 | 0 | 4 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0009 | 0/0 | 4189 | 4 | 0 | 4 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0010 | 0/0 | 4191 | 3 | 3 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0011 | 0/0 | 4185 | 3 | 0 | 1 | 0 | 1 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0012 | 0/0 | 4189 | 3 | 0 | 1 | 0 | 2 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0013 | 0/0 | 4189 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0014 | 0/0 | 4189 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0015 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0016 | 0/0 | 4191 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0017 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0018 | 0/0 | 4189 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0019 | 0/0 | 4191 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0020 | 0/0 | 4189 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0021 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0022 | 1/0 | 4191 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0023 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0024 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0025 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0026 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0027 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0028 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0029 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0030 | 0/0 | 4187 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0031 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0032 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0033 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| t0034 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 11781 | 66 | 23 | 16 | 13 | 3 | 10 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0016 | 0/0 | 11781 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0017 | 0/0 | 11781 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0027 | 0/0 | 11781 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002c0002 | 0/0 | 11781 | 41 | 11 | 12 | 6 | 6 | 6 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002c0008 | 0/0 | 11781 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002c0018 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002c0019 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002c0020 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003c0003 | 0/0 | 11781 | 15 | 14 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003c0004 | 1/0 | 11781 | 14 | 6 | 3 | 0 | 3 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003c0023 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003c0033 | 0/0 | 11781 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0004c0006 | 0/0 | 11781 | 4 | 1 | 2 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0004c0022 | 0/0 | 11781 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0005c0007 | 0/0 | 11781 | 3 | 3 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0005c0032 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0005c0034 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0006c0005 | 0/0 | 11781 | 4 | 0 | 0 | 4 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0007c0013 | 0/0 | 11781 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0008c0015 | 0/0 | 11781 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0009c0014 | 0/0 | 11781 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0010c0009 | 0/0 | 11781 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0011c0010 | 0/0 | 11781 | 2 | 0 | 0 | 2 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0012c0011 | 0/0 | 11781 | 2 | 0 | 0 | 1 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0013c0012 | 0/0 | 11781 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0014c0037 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0015c0035 | 0/0 | 11781 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0016c0021 | 0/0 | 11781 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0017c0038 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0018c0031 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0019c0026 | 0/0 | 11781 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0020c0030 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0021c0025 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0022c0024 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0023c0028 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0024c0029 | 0/0 | 11781 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0025c0036 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 15969 | 25 | 5 | 5 | 9 | 0 | 6 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0003 | 0/1 | 15969 | 21 | 14 | 4 | 0 | 0 | 2 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0007 | 0/0 | 15969 | 3 | 3 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0009 | 0/0 | 15969 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0011 | 0/0 | 15965 | 3 | 0 | 1 | 0 | 1 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0012 | 0/0 | 15969 | 3 | 0 | 1 | 0 | 2 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0018 | 0/0 | 15969 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0019 | 0/0 | 15971 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0020 | 0/0 | 15969 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0021 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0026 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0029 | 0/0 | 15971 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0030 | 0/0 | 15967 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0031 | 0/0 | 15959 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0001t0032 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0016t0003 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0017t0002 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0001c0027t0003 | 0/0 | 15969 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002c0002t0001 | 0/0 | 15969 | 35 | 11 | 9 | 4 | 6 | 5 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002c0002t0005 | 0/0 | 15969 | 4 | 0 | 3 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002c0002t0016 | 0/0 | 15971 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002c0002t0017 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002c0008t0001 | 0/0 | 15969 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002c0018t0001 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002c0019t0001 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0002c0020t0024 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003c0003t0004 | 0/0 | 15971 | 11 | 10 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003c0003t0010 | 0/0 | 15971 | 3 | 3 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003c0003t0014 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003c0004t0004 | 0/0 | 15971 | 6 | 3 | 3 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003c0004t0006 | 0/0 | 15971 | 6 | 2 | 0 | 0 | 3 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003c0004t0022 | 1/0 | 15971 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003c0004t0023 | 0/0 | 15971 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003c0023t0014 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0003c0033t0004 | 0/0 | 15971 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0004c0006t0002 | 0/0 | 15969 | 4 | 1 | 2 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0004c0022t0002 | 0/0 | 15969 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0005c0007t0007 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0005c0007t0033 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0005c0007t0034 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0005c0032t0007 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0005c0034t0015 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0006c0005t0008 | 0/0 | 15969 | 4 | 0 | 0 | 4 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0007c0013t0013 | 0/0 | 15969 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0008c0015t0002 | 0/0 | 15969 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0009c0014t0009 | 0/0 | 15969 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0010c0009t0001 | 0/0 | 15969 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0011c0010t0001 | 0/0 | 15969 | 2 | 0 | 0 | 2 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0012c0011t0001 | 0/0 | 15969 | 2 | 0 | 0 | 1 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0013c0012t0005 | 0/0 | 15969 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0014c0037t0025 | 0/0 | 15971 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0015c0035t0002 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0016c0021t0002 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0017c0038t0027 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0018c0031t0002 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0019c0026t0002 | 0/0 | 15969 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0020c0030t0002 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0021c0025t0028 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0022c0024t0007 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0023c0028t0003 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0024c0029t0003 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| a0025c0036t0001 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | copy fasta | chr3 | 49549477 | 49676549 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0009g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0009g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0011g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0011g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0011g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0012g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0012g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0012g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0018g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0019g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0020g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0021g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0026g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0029g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0030g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0031g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0001t0032g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0016t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0017t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0001c0027t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0016g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0002t0017g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0008t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0008t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0018t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0019t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0002c0020t0024g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0010g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0003t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0006g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0006g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0006g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0006g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0022g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0004t0023g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0023t0014g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0003c0033t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0004c0006t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0004c0006t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0004c0006t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0004c0006t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0004c0022t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0005c0007t0007g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0005c0007t0033g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0005c0007t0034g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0005c0032t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0005c0034t0015g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0006c0005t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0006c0005t0008g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0006c0005t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0006c0005t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0007c0013t0013g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0007c0013t0013g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0008c0015t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0008c0015t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0009c0014t0009g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0009c0014t0009g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0010c0009t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0010c0009t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0011c0010t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0011c0010t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0012c0011t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0012c0011t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0013c0012t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0013c0012t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0014c0037t0025g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0015c0035t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0016c0021t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0017c0038t0027g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0018c0031t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0019c0026t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0020c0030t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0021c0025t0028g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0022c0024t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0023c0028t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0024c0029t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| a0025c0036t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0087 | EUR | GBR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00099 | hp2 | a0020 | c0030 | t0002 | g0143 | EUR | GBR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00140 | hp1 | a0004 | c0006 | t0002 | g0037 | EUR | GBR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00140 | hp2 | a0025 | c0036 | t0001 | g0060 | EUR | GBR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00280 | hp1 | a0001 | c0001 | t0012 | g0136 | EUR | FIN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0059 | EUR | FIN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0082 | EUR | FIN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00323 | hp2 | a0001 | c0001 | t0011 | g0127 | EUR | FIN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00544 | hp1 | a0001 | c0001 | t0032 | g0144 | EAS | CHS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00544 | hp2 | a0012 | c0011 | t0001 | g0067 | EAS | CHS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00642 | hp1 | a0001 | c0001 | t0012 | g0057 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00733 | hp2 | a0004 | c0006 | t0002 | g0035 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG00735 | hp2 | a0001 | c0001 | t0018 | g0109 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0081 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01069 | hp2 | a0003 | c0033 | t0004 | g0025 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01070 | hp1 | a0003 | c0004 | t0004 | g0024 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01070 | hp2 | a0002 | c0008 | t0001 | g0173 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01071 | hp2 | a0002 | c0008 | t0001 | g0169 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01074 | hp1 | a0019 | c0026 | t0002 | g0100 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01074 | hp2 | a0003 | c0003 | t0004 | g0019 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01081 | hp1 | a0002 | c0002 | t0005 | g0074 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01081 | hp2 | a0009 | c0014 | t0009 | g0042 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0125 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01109 | hp1 | a0001 | c0001 | t0031 | g0142 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0168 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01167 | hp2 | a0001 | c0027 | t0003 | g0186 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01168 | hp2 | a0002 | c0002 | t0005 | g0062 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01192 | hp1 | a0009 | c0014 | t0009 | g0099 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01192 | hp2 | a0003 | c0004 | t0004 | g0026 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01257 | hp1 | a0013 | c0012 | t0005 | g0084 | AMR | CLM | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0119 | AMR | CLM | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01258 | hp1 | a0013 | c0012 | t0005 | g0085 | AMR | CLM | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01433 | hp1 | a0004 | c0022 | t0002 | g0034 | AMR | CLM | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01433 | hp2 | a0002 | c0002 | t0005 | g0075 | AMR | CLM | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0175 | EUR | IBS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01515 | hp2 | a0001 | c0001 | t0012 | g0116 | EUR | IBS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01516 | hp1 | a0003 | c0004 | t0006 | g0029 | EUR | IBS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01516 | hp2 | a0002 | c0019 | t0001 | g0056 | EUR | IBS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0174 | EUR | IBS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01517 | hp2 | a0003 | c0004 | t0006 | g0032 | EUR | IBS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01884 | hp1 | a0003 | c0003 | t0004 | g0022 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01884 | hp2 | a0014 | c0037 | t0025 | g0052 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01891 | hp1 | a0008 | c0015 | t0002 | g0108 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01928 | hp1 | a0001 | c0001 | t0020 | g0092 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01928 | hp2 | a0001 | c0001 | t0009 | g0149 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0152 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01981 | hp1 | a0003 | c0004 | t0004 | g0038 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0132 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02257 | hp1 | a0003 | c0004 | t0006 | g0033 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02300 | hp1 | a0004 | c0006 | t0002 | g0179 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02300 | hp2 | a0001 | c0001 | t0009 | g0094 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02451 | hp2 | a0005 | c0007 | t0034 | g0004 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02572 | hp2 | a0007 | c0013 | t0013 | g0051 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02602 | hp1 | a0021 | c0025 | t0028 | g0101 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02615 | hp2 | a0003 | c0004 | t0006 | g0117 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02622 | hp1 | a0003 | c0003 | t0010 | g0010 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02683 | hp1 | a0017 | c0038 | t0027 | g0003 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0077 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0043 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02723 | hp2 | a0002 | c0020 | t0024 | g0166 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02735 | hp1 | a0012 | c0011 | t0001 | g0066 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02735 | hp2 | a0001 | c0001 | t0011 | g0098 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0053 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02895 | hp1 | a0005 | c0034 | t0015 | g0001 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02895 | hp2 | a0003 | c0003 | t0010 | g0012 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02896 | hp1 | a0003 | c0003 | t0010 | g0011 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02922 | hp1 | a0007 | c0013 | t0013 | g0050 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02965 | hp1 | a0003 | c0003 | t0004 | g0018 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02970 | hp1 | a0022 | c0024 | t0007 | g0008 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0184 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02976 | hp1 | a0003 | c0003 | t0004 | g0016 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02976 | hp2 | a0010 | c0009 | t0001 | g0073 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03041 | hp1 | a0003 | c0003 | t0014 | g0160 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03098 | hp1 | a0003 | c0004 | t0004 | g0027 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03130 | hp2 | a0005 | c0007 | t0007 | g0002 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03139 | hp2 | a0003 | c0003 | t0004 | g0020 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03195 | hp2 | a0003 | c0003 | t0004 | g0023 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03225 | hp1 | a0003 | c0004 | t0004 | g0015 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03225 | hp2 | a0002 | c0018 | t0001 | g0009 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03453 | hp2 | a0003 | c0023 | t0014 | g0157 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03516 | hp1 | a0003 | c0003 | t0004 | g0017 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03516 | hp2 | a0008 | c0015 | t0002 | g0103 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0130 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03654 | hp2 | a0002 | c0002 | t0017 | g0058 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03710 | hp1 | a0023 | c0028 | t0003 | g0150 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0170 | SAS | BEB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03834 | hp2 | a0003 | c0004 | t0006 | g0030 | SAS | BEB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0055 | SAS | BEB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG04115 | hp1 | a0018 | c0031 | t0002 | g0091 | SAS | STU | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG04115 | hp2 | a0001 | c0001 | t0021 | g0145 | SAS | STU | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0096 | SAS | STU | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | STU | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | YRI | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | YRI | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18612 | hp1 | a0001 | c0001 | t0030 | g0121 | EAS | CHB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | CHB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18906 | hp1 | a0003 | c0003 | t0004 | g0046 | AFR | YRI | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | YRI | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18951 | hp1 | a0016 | c0021 | t0002 | g0111 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18951 | hp2 | a0006 | c0005 | t0008 | g0064 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18963 | hp1 | a0011 | c0010 | t0001 | g0165 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18979 | hp2 | a0001 | c0016 | t0003 | g0164 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18995 | hp1 | a0001 | c0001 | t0019 | g0093 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA18995 | hp2 | a0015 | c0035 | t0002 | g0134 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19000 | hp1 | a0006 | c0005 | t0008 | g0162 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19003 | hp1 | a0002 | c0002 | t0016 | g0040 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19003 | hp2 | a0001 | c0017 | t0002 | g0106 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19012 | hp1 | a0002 | c0002 | t0005 | g0039 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19030 | hp1 | a0003 | c0004 | t0023 | g0045 | AFR | LWK | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19030 | hp2 | a0003 | c0003 | t0004 | g0013 | AFR | LWK | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19043 | hp1 | a0003 | c0004 | t0004 | g0028 | AFR | LWK | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19043 | hp2 | a0024 | c0029 | t0003 | g0049 | AFR | LWK | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19065 | hp1 | a0011 | c0010 | t0001 | g0065 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19070 | hp1 | a0006 | c0005 | t0008 | g0068 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19079 | hp1 | a0001 | c0001 | t0026 | g0146 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA19079 | hp2 | a0006 | c0005 | t0008 | g0069 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA20129 | hp1 | a0010 | c0009 | t0001 | g0072 | AFR | ASW | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA20129 | hp2 | a0003 | c0003 | t0004 | g0014 | AFR | ASW | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA20752 | hp1 | a0003 | c0004 | t0006 | g0031 | EUR | TSI | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0061 | EUR | TSI | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0182 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02109 | hp2 | a0004 | c0006 | t0002 | g0036 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02486 | hp1 | a0005 | c0007 | t0033 | g0005 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03471 | hp1 | a0003 | c0003 | t0004 | g0021 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0076 | AFR | USA | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| HG06807 | hp2 | a0001 | c0001 | t0029 | g0158 | AFR | USA | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | USA | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| NA20300 | hp2 | a0005 | c0032 | t0007 | g0080 | AFR | USA | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0137 | REF | REF | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| homoSapiens_grch38 | hp1 | a0003 | c0004 | t0022 | g0044 | REF | REF | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49642892
|
A | C | 1 | a0014 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1258A>C | p.Met420Leu | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/12 | 1384/15971 | 1258/11781 | 420/3926 | chr3 | 49642892 | ||
| chr3:49651574
|
C | T | 1 | a0025 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.2018C>T | p.Ala673Val | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 2144/15971 | 2018/11781 | 673/3926 | chr3 | 49651574 | ||
| chr3:49651777
|
G | A | 8 | a0002a0006a0010others(5): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
missense_variant | MODERATE | c.2221G>A | p.Ala741Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 2347/15971 | 2221/11781 | 741/3926 | chr3 | 49651777 | ||
| chr3:49652209
|
C | T | 1 | a0013 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.2653C>T | p.Pro885Ser | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 2779/15971 | 2653/11781 | 885/3926 | chr3 | 49652209 | ||
| chr3:49652590
|
C | T | 1 | a0015 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.3034C>T | p.Arg1012Cys | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3160/15971 | 3034/11781 | 1012/3926 | chr3 | 49652590 | ||
| chr3:49652816
|
G | A | 1 | a0016 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.3260G>A | p.Arg1087Gln | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3386/15971 | 3260/11781 | 1087/3926 | chr3 | 49652816 | ||
| chr3:49653187
|
C | T | 3 | a0006a0011a0012 | 8 | HG00544.hp2 HG02735.hp1 NA18951.hp2 others(5): Show |
missense_variant | MODERATE | c.3631C>T | p.Pro1211Ser | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3757/15971 | 3631/11781 | 1211/3926 | chr3 | 49653187 | ||
| chr3:49653194
|
G | A | 1 | a0004 | 5 | HG00140.hp1 HG00733.hp2 HG01433.hp1 others(2): Show |
missense_variant | MODERATE | c.3638G>A | p.Gly1213Asp | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3764/15971 | 3638/11781 | 1213/3926 | chr3 | 49653194 | ||
| chr3:49653251
|
C | T | 2 | a0005a0017 | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
missense_variant | MODERATE | c.3695C>T | p.Thr1232Ile | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3821/15971 | 3695/11781 | 1232/3926 | chr3 | 49653251 | ||
| chr3:49653857
|
A | G | 1 | a0010 | 2 | HG02976.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.4301A>G | p.Asp1434Gly | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 4427/15971 | 4301/11781 | 1434/3926 | chr3 | 49653857 | ||
| chr3:49654049
|
C | T | 1 | a0007 | 2 | HG02572.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.4493C>T | p.Pro1498Leu | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 4619/15971 | 4493/11781 | 1498/3926 | chr3 | 49654049 | ||
| chr3:49654186
|
C | T | 1 | a0018 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.4630C>T | p.Arg1544Cys | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 4756/15971 | 4630/11781 | 1544/3926 | chr3 | 49654186 | ||
| chr3:49654663
|
A | G | 1 | a0024 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.5107A>G | p.Ile1703Val | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 5233/15971 | 5107/11781 | 1703/3926 | chr3 | 49654663 | ||
| chr3:49655422
|
C | T | 1 | a0023 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.5866C>T | p.Arg1956Trp | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 5992/15971 | 5866/11781 | 1956/3926 | chr3 | 49655422 | ||
| chr3:49655477
|
A | C | 1 | a0008 | 2 | HG01891.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.5921A>C | p.Gln1974Pro | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 6047/15971 | 5921/11781 | 1974/3926 | chr3 | 49655477 | ||
| chr3:49656067
|
G | A | 1 | a0022 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.6511G>A | p.Ala2171Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 6637/15971 | 6511/11781 | 2171/3926 | chr3 | 49656067 | ||
| chr3:49656970
|
C | T | 1 | a0009 | 2 | HG01081.hp2 HG01192.hp1 |
missense_variant | MODERATE | c.7414C>T | p.Arg2472Trp | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 7540/15971 | 7414/11781 | 2472/3926 | chr3 | 49656970 | ||
| chr3:49657006
|
C | A | 1 | a0021 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.7450C>A | p.Pro2484Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 7576/15971 | 7450/11781 | 2484/3926 | chr3 | 49657006 | ||
| chr3:49658069
|
C | T | 1 | a0014 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.8513C>T | p.Thr2838Met | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 8639/15971 | 8513/11781 | 2838/3926 | chr3 | 49658069 | ||
| chr3:49660642
|
G | A | 1 | a0019 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.8797G>A | p.Val2933Ile | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 6/12 | 8923/15971 | 8797/11781 | 2933/3926 | chr3 | 49660642 | ||
| chr3:49660682
|
G | A | 1 | a0020 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.8837G>A | p.Arg2946Gln | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 6/12 | 8963/15971 | 8837/11781 | 2946/3926 | chr3 | 49660682 | ||
| chr3:49663146
|
G | T | 1 | a0012 | 2 | HG00544.hp2 HG02735.hp1 |
missense_variant | MODERATE | c.10988G>T | p.Gly3663Val | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 7/12 | 11114/15971 | 10988/11781 | 3663/3926 | chr3 | 49663146 | ||
| chr3:49663442
|
C | A | 1 | a0017 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.11284C>A | p.Pro3762Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 7/12 | 11410/15971 | 11284/11781 | 3762/3926 | chr3 | 49663442 | ||
| chr3:49663647
|
G | A | 1 | a0012 | 2 | HG00544.hp2 HG02735.hp1 |
missense_variant | MODERATE | c.11489G>A | p.Gly3830Asp | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 7/12 | 11615/15971 | 11489/11781 | 3830/3926 | chr3 | 49663647 | ||
| chr3:49663865
|
G | A | 17 | a0001a0004a0005others(14): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
missense_variant | MODERATE | c.11587G>A | p.Ala3863Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 8/12 | 11713/15971 | 11587/11781 | 3863/3926 | chr3 | 49663865 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49554644
|
G | A | 1 | a0001c0016 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.42G>A | p.Gly14Gly | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/12 | 168/15971 | 42/11781 | 14/3926 | chr3 | 49554644 | ||
| chr3:49554713
|
T | C | 1 | a0001c0017 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.111T>C | p.Pro37Pro | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/12 | 237/15971 | 111/11781 | 37/3926 | chr3 | 49554713 | ||
| chr3:49554794
|
C | T | 1 | a0017c0038 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.192C>T | p.Gly64Gly | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/12 | 318/15971 | 192/11781 | 64/3926 | chr3 | 49554794 | ||
| chr3:49642624
|
C | T | 1 | a0017c0038 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.990C>T | p.Thr330Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/12 | 1116/15971 | 990/11781 | 330/3926 | chr3 | 49642624 | ||
| chr3:49652736
|
G | T | 1 | a0005c0034 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.3180G>T | p.Arg1060Arg | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3306/15971 | 3180/11781 | 1060/3926 | chr3 | 49652736 | ||
| chr3:49652766
|
G | A | 36 | a0001c0001a0001c0016a0001c0017others(33): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
synonymous_variant | LOW | c.3210G>A | p.Thr1070Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3336/15971 | 3210/11781 | 1070/3926 | chr3 | 49652766 | ||
| chr3:49652895
|
C | T | 1 | a0002c0020 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.3339C>T | p.Ala1113Ala | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3465/15971 | 3339/11781 | 1113/3926 | chr3 | 49652895 | ||
| chr3:49653063
|
C | T | 11 | a0002c0002a0002c0018a0002c0019others(8): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
synonymous_variant | LOW | c.3507C>T | p.Ser1169Ser | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3633/15971 | 3507/11781 | 1169/3926 | chr3 | 49653063 | ||
| chr3:49653351
|
G | A | 1 | a0007c0013 | 2 | HG02572.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.3795G>A | p.Gln1265Gln | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3921/15971 | 3795/11781 | 1265/3926 | chr3 | 49653351 | ||
| chr3:49654242
|
A | G | 1 | a0020c0030 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.4686A>G | p.Ala1562Ala | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 4812/15971 | 4686/11781 | 1562/3926 | chr3 | 49654242 | ||
| chr3:49655400
|
G | A | 1 | a0004c0022 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.5844G>A | p.Glu1948Glu | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 5970/15971 | 5844/11781 | 1948/3926 | chr3 | 49655400 | ||
| chr3:49655496
|
G | A | 1 | a0003c0023 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.5940G>A | p.Leu1980Leu | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 6066/15971 | 5940/11781 | 1980/3926 | chr3 | 49655496 | ||
| chr3:49655589
|
C | T | 1 | a0002c0019 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.6033C>T | p.Asp2011Asp | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 6159/15971 | 6033/11781 | 2011/3926 | chr3 | 49655589 | ||
| chr3:49656606
|
C | T | 1 | a0003c0033 | 1 | HG01069.hp2 | synonymous_variant | LOW | c.7050C>T | p.Ser2350Ser | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 7176/15971 | 7050/11781 | 2350/3926 | chr3 | 49656606 | ||
| chr3:49661262
|
T | C | 1 | a0002c0018 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.9417T>C | p.Arg3139Arg | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 6/12 | 9543/15971 | 9417/11781 | 3139/3926 | chr3 | 49661262 | ||
| chr3:49662090
|
C | T | 1 | a0005c0032 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.10245C>T | p.Asn3415Asn | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 6/12 | 10371/15971 | 10245/11781 | 3415/3926 | chr3 | 49662090 | ||
| chr3:49664526
|
A | G | 1 | a0001c0027 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.11712A>G | p.Ala3904Ala | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 9/12 | 11838/15971 | 11712/11781 | 3904/3926 | chr3 | 49664526 | ||
| chr3:49664550
|
G | A | 9 | a0002c0002a0002c0008a0002c0018others(6): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
synonymous_variant | LOW | c.11736G>A | p.Thr3912Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 9/12 | 11862/15971 | 11736/11781 | 3912/3926 | chr3 | 49664550 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49667609
|
C | G | 1 | a0005c0007t0034 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*124C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 2770 | chr3 | 49667609 | |||||
| chr3:49667832
|
C | T | 2 | a0003c0003t0014a0003c0023t0014 | 2 | HG03041.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*347C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 2993 | chr3 | 49667832 | |||||
| chr3:49668054
|
C | A | 1 | a0007c0013t0013 | 2 | HG02572.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*569C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 3215 | chr3 | 49668054 | |||||
| chr3:49668057
|
G | A | 1 | a0005c0034t0015 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*572G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 3218 | chr3 | 49668057 | |||||
| chr3:49668079
|
T | A | 12 | a0002c0002t0001a0002c0002t0005a0002c0002t0016others(9): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*594T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 3240 | chr3 | 49668079 | |||||
| chr3:49668285
|
G | A | 1 | a0001c0001t0018 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*800G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 3446 | chr3 | 49668285 | |||||
| chr3:49668317
|
C | T | 1 | a0002c0002t0017 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*832C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 3478 | chr3 | 49668317 | |||||
| chr3:49668552
|
G | C | 2 | a0001c0001t0019a0001c0001t0020 | 2 | HG01928.hp1 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1067G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 3713 | chr3 | 49668552 | |||||
| chr3:49668916
|
T | C | 1 | a0001c0001t0021 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1431T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4077 | chr3 | 49668916 | |||||
| chr3:49669241
|
G | A | 1 | a0003c0003t0010 | 3 | HG02622.hp1 HG02895.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1756G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4402 | chr3 | 49669241 | |||||
| chr3:49669266
|
A | G | 3 | a0002c0002t0005a0002c0002t0016a0013c0012t0005 | 7 | HG01081.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1781A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4427 | chr3 | 49669266 | |||||
| chr3:49669303
|
G | C | 1 | a0003c0004t0006 | 6 | HG01516.hp1 HG01517.hp2 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1818G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4464 | chr3 | 49669303 | |||||
| chr3:49669305
|
C | T | 38 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(35): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1820C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4466 | chr3 | 49669305 | |||||
| chr3:49669401
|
T | C | 1 | a0001c0001t0026 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1916T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4562 | chr3 | 49669401 | |||||
| chr3:49669799
|
C | T | 2 | a0003c0003t0014a0003c0023t0014 | 2 | HG03041.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2314C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4960 | chr3 | 49669799 | |||||
| chr3:49670132
|
C | T | 1 | a0005c0007t0033 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2647C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 5293 | chr3 | 49670132 | |||||
| chr3:49670215
|
C | T | 60 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(57): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*2730C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 5376 | chr3 | 49670215 | |||||
| chr3:49670470
|
C | T | 2 | a0003c0003t0014a0003c0023t0014 | 2 | HG03041.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2985C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 5631 | chr3 | 49670470 | |||||
| chr3:49670618
|
T | G | 2 | a0001c0001t0009a0009c0014t0009 | 4 | HG01081.hp2 HG01192.hp1 HG01928.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3133T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 5779 | chr3 | 49670618 | |||||
| chr3:49670923
|
C | T | 1 | a0014c0037t0025 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3438C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6084 | chr3 | 49670923 | |||||
| chr3:49671019
|
C | T | 1 | a0001c0001t0032 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3534C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6180 | chr3 | 49671019 | |||||
| chr3:49671069
|
G | T | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(27): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*3584G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6230 | chr3 | 49671069 | |||||
| chr3:49671110
|
T | C | 1 | a0021c0025t0028 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3625T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6271 | chr3 | 49671110 | |||||
| chr3:49671149
|
C | T | 1 | a0001c0001t0012 | 3 | HG00280.hp1 HG00642.hp1 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3664C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6310 | chr3 | 49671149 | |||||
| chr3:49671153
|
CGTGCGTG others(5): Show |
C | 1 | a0001c0001t0031 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3672_*3683delCGTG others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6318 | INFO_REALIGN_3_PRIME | chr3 | 49671153 | ||||
| chr3:49671155
|
TGC | T | 49 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(46): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*3672_*3673delCG | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6318 | INFO_REALIGN_3_PRIME | chr3 | 49671155 | ||||
| chr3:49671157
|
C | T | 10 | a0001c0001t0019a0001c0001t0030a0002c0002t0016others(7): Show | 32 | HG01069.hp2 HG01070.hp1 HG01074.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3672C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6318 | chr3 | 49671157 | |||||
| chr3:49671336
|
T | C | 18 | a0001c0001t0002a0001c0001t0009a0001c0001t0012others(15): Show | 53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3851T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6497 | chr3 | 49671336 | |||||
| chr3:49671370
|
TCAAA | T | 2 | a0001c0001t0011a0001c0001t0030 | 4 | HG00323.hp2 HG01106.hp2 HG02735.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3893_*3896delACAA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6539 | INFO_REALIGN_3_PRIME | chr3 | 49671370 | ||||
| chr3:49671465
|
C | T | 1 | a0017c0038t0027 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3980C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6626 | chr3 | 49671465 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49554951
|
C | T | 1 | a0001c0027t0003g0186 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.224+125C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49554951 | ||||||
| chr3:49555427
|
T | A | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+601T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49555427 | ||||||
| chr3:49555534
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0002c0018t0001g0009others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+708G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49555534 | ||||||
| chr3:49555976
|
A | G | 6 | a0002c0002t0001g0180a0002c0002t0001g0181a0002c0002t0001g0182others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.224+1150A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49555976 | ||||||
| chr3:49555977
|
G | T | 6 | a0002c0002t0001g0180a0002c0002t0001g0181a0002c0002t0001g0182others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.224+1151G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49555977 | ||||||
| chr3:49556165
|
G | A | 14 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0016others(11): Show | 14 | HG01074.hp2 HG01884.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.224+1339G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49556165 | ||||||
| chr3:49556322
|
A | G | 1 | a0004c0006t0002g0179 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.224+1496A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49556322 | ||||||
| chr3:49556627
|
T | C | 16 | a0003c0004t0004g0024a0003c0004t0004g0026a0003c0004t0004g0027others(13): Show | 16 | HG00140.hp1 HG00733.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.224+1801T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49556627 | ||||||
| chr3:49556918
|
T | C | 2 | a0002c0002t0005g0039a0002c0002t0016g0040 | 2 | NA19003.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.224+2092T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49556918 | ||||||
| chr3:49556927
|
G | T | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02004.hp2 NA19000.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.224+2101G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49556927 | ||||||
| chr3:49557227
|
A | G | 1 | a0005c0007t0033g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.224+2401A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49557227 | ||||||
| chr3:49557307
|
C | T | 10 | a0003c0003t0004g0014a0003c0003t0004g0016a0003c0003t0004g0017others(7): Show | 10 | HG01074.hp2 HG01884.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.224+2481C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49557307 | ||||||
| chr3:49557558
|
T | TGGA | 9 | a0002c0002t0001g0167a0002c0002t0001g0168a0002c0002t0001g0170others(6): Show | 9 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.224+2733_224+2735d others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49557558 | |||||
| chr3:49557575
|
G | GT | 14 | a0001c0001t0002g0161a0001c0001t0003g0153a0001c0001t0003g0154others(11): Show | 14 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.224+2769dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49557575 | |||||
| chr3:49557575
|
GT | G | 7 | a0001c0001t0003g0041a0005c0007t0007g0002a0005c0007t0033g0005others(4): Show | 7 | HG01081.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.224+2769delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49557575 | |||||
| chr3:49557992
|
C | T | 7 | a0002c0002t0001g0152a0002c0002t0001g0180a0002c0002t0001g0181others(4): Show | 7 | HG01891.hp2 HG01934.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.224+3166C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49557992 | ||||||
| chr3:49558353
|
C | T | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.224+3527C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49558353 | ||||||
| chr3:49559029
|
C | T | 144 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.224+4203C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559029 | ||||||
| chr3:49559160
|
C | G | 68 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.224+4334C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559160 | ||||||
| chr3:49559227
|
G | A | 1 | a0018c0031t0002g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.224+4401G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559227 | ||||||
| chr3:49559370
|
A | C | 1 | a0001c0001t0002g0151 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.224+4544A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559370 | ||||||
| chr3:49559580
|
C | T | 62 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.224+4754C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559580 | ||||||
| chr3:49559622
|
C | T | 13 | a0001c0016t0003g0164a0002c0002t0001g0088a0002c0002t0001g0089others(10): Show | 13 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.224+4796C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559622 | ||||||
| chr3:49559646
|
T | A | 1 | a0001c0001t0020g0092 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.224+4820T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559646 | ||||||
| chr3:49559696
|
T | G | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224+4870T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559696 | ||||||
| chr3:49559797
|
C | G | 60 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.224+4971C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559797 | ||||||
| chr3:49559880
|
G | T | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5054G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559880 | ||||||
| chr3:49559881
|
A | C | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5055A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559881 | ||||||
| chr3:49559882
|
G | T | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5056G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559882 | ||||||
| chr3:49559886
|
A | T | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5060A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559886 | ||||||
| chr3:49559888
|
T | A | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5062T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559888 | ||||||
| chr3:49559889
|
G | A | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5063G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559889 | ||||||
| chr3:49559892
|
G | A | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5066G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559892 | ||||||
| chr3:49559894
|
C | G | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5068C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559894 | ||||||
| chr3:49559895
|
T | C | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5069T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559895 | ||||||
| chr3:49559906
|
A | T | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5080A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559906 | ||||||
| chr3:49559931
|
G | T | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5105G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559931 | ||||||
| chr3:49559944
|
G | A | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5118G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559944 | ||||||
| chr3:49559945
|
G | T | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5119G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559945 | ||||||
| chr3:49559948
|
A | G | 1 | a0002c0002t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5122A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559948 | ||||||
| chr3:49560075
|
T | C | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224+5249T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49560075 | ||||||
| chr3:49560304
|
T | C | 62 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.224+5478T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49560304 | ||||||
| chr3:49560631
|
T | C | 144 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.224+5805T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49560631 | ||||||
| chr3:49561550
|
T | A | 1 | a0002c0002t0005g0039 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.224+6724T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49561550 | ||||||
| chr3:49561706
|
A | C | 1 | a0003c0003t0014g0160 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.224+6880A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49561706 | ||||||
| chr3:49561968
|
C | T | 2 | a0001c0001t0003g0159a0001c0001t0029g0158 | 2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.224+7142C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49561968 | ||||||
| chr3:49562187
|
C | T | 2 | a0002c0002t0001g0174a0002c0002t0001g0175 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.224+7361C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49562187 | ||||||
| chr3:49562345
|
A | G | 1 | a0023c0028t0003g0150 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.224+7519A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49562345 | ||||||
| chr3:49562440
|
TAAATTAG others(45): Show |
T | 1 | a0018c0031t0002g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.224+7616_224+7667d others(54): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49562440 | |||||
| chr3:49562816
|
G | A | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+7990G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49562816 | ||||||
| chr3:49562886
|
G | A | 152 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.224+8060G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49562886 | ||||||
| chr3:49562993
|
C | T | 82 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.224+8167C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49562993 | ||||||
| chr3:49563396
|
A | G | 1 | a0002c0002t0001g0087 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.224+8570A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49563396 | ||||||
| chr3:49563822
|
T | C | 152 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.224+8996T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49563822 | ||||||
| chr3:49564014
|
C | T | 1 | a0003c0003t0004g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.224+9188C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49564014 | ||||||
| chr3:49564066
|
C | T | 2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.224+9240C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49564066 | ||||||
| chr3:49564556
|
C | T | 1 | a0001c0001t0009g0149 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.224+9730C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49564556 | ||||||
| chr3:49564799
|
C | A | 1 | a0001c0001t0007g0043 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.224+9973C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49564799 | ||||||
| chr3:49564995
|
TA | T | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+10181delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49564995 | |||||
| chr3:49565144
|
C | CT | 58 | a0001c0001t0002g0161a0001c0001t0012g0057a0002c0002t0001g0055others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.224+10337dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49565144 | |||||
| chr3:49565148
|
T | C | 1 | a0001c0001t0019g0093 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.224+10322T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565148 | ||||||
| chr3:49565304
|
G | C | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0002c0018t0001g0009 | 3 | HG02257.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.224+10478G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565304 | ||||||
| chr3:49565313
|
AT | A | 141 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.224+10509delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49565313 | |||||
| chr3:49565359
|
C | T | 1 | a0003c0003t0004g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.224+10533C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565359 | ||||||
| chr3:49565567
|
G | A | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+10741G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565567 | ||||||
| chr3:49565736
|
A | G | 1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.224+10910A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565736 | ||||||
| chr3:49565800
|
C | T | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224+10974C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565800 | ||||||
| chr3:49565853
|
G | A | 1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.224+11027G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565853 | ||||||
| chr3:49565856
|
C | T | 60 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.224+11030C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565856 | ||||||
| chr3:49565995
|
G | A | 2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.224+11169G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565995 | ||||||
| chr3:49566491
|
A | C | 1 | a0003c0004t0004g0038 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.224+11665A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49566491 | ||||||
| chr3:49566600
|
C | T | 1 | a0003c0023t0014g0157 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.224+11774C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49566600 | ||||||
| chr3:49566788
|
GA | G | 86 | a0001c0001t0002g0102a0001c0001t0002g0104a0001c0001t0002g0105others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.224+11984delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49566788 | |||||
| chr3:49566865
|
G | GT | 68 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.224+12049dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49566865 | |||||
| chr3:49567301
|
GCT | G | 3 | a0002c0002t0001g0081a0002c0002t0001g0082a0002c0002t0001g0083 | 3 | HG00323.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.224+12478_224+1247 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49567301 | |||||
| chr3:49567366
|
C | T | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+12540C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49567366 | ||||||
| chr3:49567471
|
G | A | 144 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.224+12645G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49567471 | ||||||
| chr3:49568116
|
C | T | 1 | a0002c0002t0001g0086 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.224+13290C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49568116 | ||||||
| chr3:49568755
|
A | C | 47 | a0001c0001t0002g0161a0001c0016t0003g0164a0002c0002t0001g0053others(44): Show | 47 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.224+13929A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49568755 | ||||||
| chr3:49568900
|
A | G | 185 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.224+14074A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49568900 | ||||||
| chr3:49568952
|
G | A | 13 | a0001c0001t0012g0057a0002c0002t0001g0054a0002c0002t0001g0055others(10): Show | 13 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.224+14126G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49568952 | ||||||
| chr3:49568996
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.224+14170C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49568996 | ||||||
| chr3:49569542
|
C | T | 1 | a0005c0032t0007g0080 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.224+14716C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49569542 | ||||||
| chr3:49569595
|
G | A | 1 | a0020c0030t0002g0143 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.224+14769G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49569595 | ||||||
| chr3:49570519
|
C | T | 1 | a0003c0003t0004g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.224+15693C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49570519 | ||||||
| chr3:49570691
|
G | C | 4 | a0001c0001t0009g0094a0001c0001t0009g0149a0009c0014t0009g0042others(1): Show | 4 | HG01081.hp2 HG01192.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+15865G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49570691 | ||||||
| chr3:49571479
|
G | A | 1 | a0001c0001t0020g0092 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.224+16653G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49571479 | ||||||
| chr3:49571693
|
C | T | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0002c0018t0001g0009others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+16867C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49571693 | ||||||
| chr3:49571799
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.224+16973C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49571799 | ||||||
| chr3:49571870
|
C | T | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+17044C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49571870 | ||||||
| chr3:49572006
|
G | A | 1 | a0003c0003t0004g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.224+17180G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572006 | ||||||
| chr3:49572044
|
C | G | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.224+17218C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572044 | ||||||
| chr3:49572141
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.224+17315A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572141 | ||||||
| chr3:49572242
|
G | C | 1 | a0019c0026t0002g0100 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.224+17416G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572242 | ||||||
| chr3:49572361
|
G | T | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.224+17535G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572361 | ||||||
| chr3:49572423
|
C | T | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+17597C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572423 | ||||||
| chr3:49572434
|
G | A | 7 | a0002c0002t0001g0152a0002c0002t0001g0180a0002c0002t0001g0181others(4): Show | 7 | HG01891.hp2 HG01934.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.224+17608G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572434 | ||||||
| chr3:49572556
|
C | T | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224+17730C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572556 | ||||||
| chr3:49572694
|
C | T | 1 | a0003c0003t0004g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.224+17868C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572694 | ||||||
| chr3:49572790
|
C | T | 61 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.224+17964C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572790 | ||||||
| chr3:49573188
|
G | A | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+18362G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573188 | ||||||
| chr3:49573281
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.224+18455G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573281 | ||||||
| chr3:49573524
|
C | T | 73 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.224+18698C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573524 | ||||||
| chr3:49573656
|
G | GT | 3 | a0001c0016t0003g0164a0002c0002t0001g0053a0002c0020t0024g0166 | 3 | HG02723.hp2 HG02738.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.224+18830_224+1883 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573656 | ||||||
| chr3:49573657
|
G | GT | 5 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+18848dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49573657 | |||||
| chr3:49573657
|
G | T | 67 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.224+18831G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573657 | ||||||
| chr3:49573932
|
C | T | 1 | a0001c0001t0003g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.224+19106C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573932 | ||||||
| chr3:49573986
|
G | A | 1 | a0001c0001t0019g0093 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.224+19160G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573986 | ||||||
| chr3:49574024
|
A | G | 62 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.224+19198A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49574024 | ||||||
| chr3:49574061
|
C | T | 3 | a0002c0002t0001g0081a0002c0002t0001g0082a0002c0002t0001g0083 | 3 | HG00323.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.224+19235C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49574061 | ||||||
| chr3:49574132
|
A | ATT | 88 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.224+19321_224+1932 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49574132 | |||||
| chr3:49574132
|
A | ATTT | 58 | a0001c0001t0002g0135a0001c0001t0002g0139a0001c0001t0002g0140others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.224+19320_224+1932 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49574132 | |||||
| chr3:49574132
|
A | ATTTT | 9 | a0002c0002t0001g0090a0002c0002t0001g0163a0002c0002t0001g0180others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.224+19319_224+1932 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49574132 | |||||
| chr3:49574227
|
CA | C | 62 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.224+19404delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49574227 | |||||
| chr3:49574233
|
T | G | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.224+19407T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49574233 | ||||||
| chr3:49574325
|
A | G | 1 | a0002c0002t0001g0152 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.224+19499A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49574325 | ||||||
| chr3:49574630
|
CT | C | 137 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.224+19827delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49574630 | |||||
| chr3:49574630
|
CTT | C | 10 | a0001c0001t0032g0144a0002c0002t0001g0063a0002c0002t0001g0081others(7): Show | 10 | HG00544.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.224+19826_224+1982 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49574630 | |||||
| chr3:49574755
|
C | T | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+19929C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49574755 | ||||||
| chr3:49574834
|
C | T | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224+20008C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49574834 | ||||||
| chr3:49575035
|
G | T | 1 | a0001c0001t0003g0132 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.224+20209G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575035 | ||||||
| chr3:49575420
|
A | G | 4 | a0002c0002t0001g0053a0002c0002t0001g0077a0002c0002t0001g0078others(1): Show | 4 | HG02055.hp2 HG02602.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+20594A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575420 | ||||||
| chr3:49575424
|
GTATA | G | 2 | a0002c0002t0001g0053a0002c0002t0001g0079 | 2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.224+20604_224+2060 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49575424 | |||||
| chr3:49575492
|
A | G | 2 | a0001c0001t0002g0131a0001c0001t0002g0139 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.224+20666A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575492 | ||||||
| chr3:49575567
|
C | T | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+20741C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575567 | ||||||
| chr3:49575601
|
A | G | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.224+20775A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575601 | ||||||
| chr3:49575644
|
A | ATG | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+20832_224+2083 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49575644 | |||||
| chr3:49575658
|
GTA | G | 103 | a0001c0001t0002g0124a0001c0001t0002g0148a0001c0001t0002g0161others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.224+20851_224+2085 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49575658 | |||||
| chr3:49575658
|
GTATA | G | 48 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(45): Show | 48 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.224+20849_224+2085 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49575658 | |||||
| chr3:49575662
|
A | G | 3 | a0001c0001t0003g0159a0001c0001t0029g0158a0014c0037t0025g0052 | 3 | HG01884.hp2 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.224+20836A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575662 | ||||||
| chr3:49575745
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.224+20919G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575745 | ||||||
| chr3:49576129
|
G | A | 1 | a0001c0001t0003g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.224+21303G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49576129 | ||||||
| chr3:49577110
|
TG | T | 2 | a0001c0001t0012g0116a0001c0001t0012g0136 | 2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.224+22285delG | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577110 | ||||||
| chr3:49577538
|
CT | C | 76 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.224+22715delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49577538 | |||||
| chr3:49577541
|
T | C | 11 | a0001c0001t0007g0006a0001c0001t0007g0007a0002c0018t0001g0009others(8): Show | 11 | HG02257.hp2 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.224+22715T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577541 | ||||||
| chr3:49577543
|
T | C | 76 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.224+22717T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577543 | ||||||
| chr3:49577769
|
A | G | 1 | a0002c0002t0001g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.224+22943A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577769 | ||||||
| chr3:49577832
|
G | A | 1 | a0002c0002t0001g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.224+23006G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577832 | ||||||
| chr3:49577884
|
G | A | 1 | a0001c0001t0003g0130 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.224+23058G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577884 | ||||||
| chr3:49577975
|
C | T | 1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.224+23149C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577975 | ||||||
| chr3:49578191
|
G | T | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.224+23365G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578191 | ||||||
| chr3:49578410
|
G | GT | 44 | a0001c0001t0002g0161a0001c0016t0003g0164a0002c0002t0001g0063others(41): Show | 44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.224+23597dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49578410 | |||||
| chr3:49578410
|
G | GTT | 15 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(12): Show | 15 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(12): Show |
intron_variant | MODIFIER | c.224+23596_224+2359 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49578410 | |||||
| chr3:49578410
|
GT | G | 72 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.224+23597delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49578410 | |||||
| chr3:49578620
|
G | GA | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.224+23794_224+2379 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578620 | ||||||
| chr3:49578621
|
T | C | 76 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.224+23795T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578621 | ||||||
| chr3:49578630
|
T | C | 1 | a0003c0004t0006g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.224+23804T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578630 | ||||||
| chr3:49578642
|
G | A | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG01257.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.224+23816G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578642 | ||||||
| chr3:49578696
|
G | A | 1 | a0002c0002t0001g0055 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.224+23870G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578696 | ||||||
| chr3:49578894
|
G | A | 1 | a0011c0010t0001g0165 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.224+24068G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578894 | ||||||
| chr3:49579154
|
AT | A | 7 | a0002c0002t0001g0063a0002c0002t0001g0175a0002c0002t0005g0039others(4): Show | 7 | HG01070.hp2 HG01081.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.224+24344delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49579154 | |||||
| chr3:49579564
|
A | G | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.224+24738A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49579564 | ||||||
| chr3:49579584
|
C | CT | 11 | a0002c0002t0001g0053a0002c0002t0001g0077a0002c0002t0001g0078others(8): Show | 11 | HG01081.hp1 HG01168.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.224+24768dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49579584 | |||||
| chr3:49579738
|
T | C | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224+24912T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49579738 | ||||||
| chr3:49579769
|
AT | A | 87 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.224+24950delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49579769 | |||||
| chr3:49579796
|
ATTGGAAA others(23): Show |
A | 149 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.224+24972_224+2500 others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49579796 | |||||
| chr3:49580162
|
A | G | 2 | a0001c0001t0002g0097a0023c0028t0003g0150 | 2 | HG02738.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.224+25336A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49580162 | ||||||
| chr3:49580494
|
C | T | 1 | a0003c0004t0004g0038 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.224+25668C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49580494 | ||||||
| chr3:49580698
|
A | G | 1 | a0002c0002t0005g0075 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.224+25872A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49580698 | ||||||
| chr3:49580831
|
G | A | 10 | a0003c0003t0004g0014a0003c0003t0004g0016a0003c0003t0004g0017others(7): Show | 10 | HG01074.hp2 HG01884.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.224+26005G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49580831 | ||||||
| chr3:49580951
|
T | C | 1 | a0005c0032t0007g0080 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.224+26125T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49580951 | ||||||
| chr3:49580978
|
C | CT | 61 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.224+26166dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49580978 | |||||
| chr3:49581074
|
C | T | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+26248C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581074 | ||||||
| chr3:49581417
|
C | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26591C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581417 | ||||||
| chr3:49581419
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26593T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581419 | ||||||
| chr3:49581424
|
C | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26598C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581424 | ||||||
| chr3:49581428
|
T | C | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26602T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581428 | ||||||
| chr3:49581429
|
A | C | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26603A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581429 | ||||||
| chr3:49581430
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26604T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581430 | ||||||
| chr3:49581434
|
A | C | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26608A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581434 | ||||||
| chr3:49581437
|
A | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26611A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581437 | ||||||
| chr3:49581438
|
T | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26612T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581438 | ||||||
| chr3:49581439
|
A | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26613A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581439 | ||||||
| chr3:49581441
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26615T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581441 | ||||||
| chr3:49581442
|
G | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26616G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581442 | ||||||
| chr3:49581443
|
T | C | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26617T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581443 | ||||||
| chr3:49581446
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26620T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581446 | ||||||
| chr3:49581450
|
T | C | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26624T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581450 | ||||||
| chr3:49581451
|
G | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26625G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581451 | ||||||
| chr3:49581452
|
T | C | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26626T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581452 | ||||||
| chr3:49581453
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26627T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581453 | ||||||
| chr3:49581454
|
C | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26628C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581454 | ||||||
| chr3:49581455
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26629T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581455 | ||||||
| chr3:49581457
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26631T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581457 | ||||||
| chr3:49581458
|
T | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26632T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581458 | ||||||
| chr3:49581459
|
T | C | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26633T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581459 | ||||||
| chr3:49581460
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26634T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581460 | ||||||
| chr3:49581462
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26636T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581462 | ||||||
| chr3:49581463
|
T | C | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26637T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581463 | ||||||
| chr3:49581464
|
A | C | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26638A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581464 | ||||||
| chr3:49581465
|
T | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26639T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581465 | ||||||
| chr3:49581466
|
T | C | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26640T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581466 | ||||||
| chr3:49581469
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26643T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581469 | ||||||
| chr3:49581472
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26646T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581472 | ||||||
| chr3:49581473
|
T | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26647T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581473 | ||||||
| chr3:49581475
|
T | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26649T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581475 | ||||||
| chr3:49581477
|
A | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26651A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581477 | ||||||
| chr3:49581478
|
A | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26652A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581478 | ||||||
| chr3:49581479
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26653T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581479 | ||||||
| chr3:49581484
|
T | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26658T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581484 | ||||||
| chr3:49581485
|
A | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26659A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581485 | ||||||
| chr3:49581486
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26660T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581486 | ||||||
| chr3:49581487
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26661T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581487 | ||||||
| chr3:49581492
|
C | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26666C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581492 | ||||||
| chr3:49581493
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26667T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581493 | ||||||
| chr3:49581496
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26670T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581496 | ||||||
| chr3:49581497
|
T | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26671T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581497 | ||||||
| chr3:49581500
|
T | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26674T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581500 | ||||||
| chr3:49581502
|
T | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26676T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581502 | ||||||
| chr3:49581510
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26684T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581510 | ||||||
| chr3:49581511
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26685T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581511 | ||||||
| chr3:49581517
|
T | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26691T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581517 | ||||||
| chr3:49581518
|
A | G | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26692A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581518 | ||||||
| chr3:49581519
|
G | C | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26693G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581519 | ||||||
| chr3:49581520
|
G | T | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26694G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581520 | ||||||
| chr3:49581601
|
G | A | 1 | a0001c0001t0011g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.224+26775G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581601 | ||||||
| chr3:49581752
|
A | T | 1 | a0002c0002t0016g0040 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.224+26926A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581752 | ||||||
| chr3:49582060
|
C | T | 149 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.224+27234C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49582060 | ||||||
| chr3:49582072
|
T | A | 1 | a0001c0001t0003g0137 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.224+27246T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49582072 | ||||||
| chr3:49582218
|
T | C | 61 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.224+27392T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49582218 | ||||||
| chr3:49582241
|
C | T | 1 | a0002c0002t0005g0039 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.224+27415C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49582241 | ||||||
| chr3:49582952
|
C | CATTT | 42 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.224+28157_224+2816 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49582952 | |||||
| chr3:49582952
|
C | CATTTATT others(1): Show |
90 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0104others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.224+28153_224+2816 others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49582952 | |||||
| chr3:49582952
|
C | CATTTATT others(5): Show |
18 | a0001c0001t0002g0102a0001c0001t0002g0114a0001c0001t0002g0135others(15): Show | 18 | HG00323.hp2 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.224+28149_224+2816 others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49582952 | |||||
| chr3:49582952
|
C | CATTTATT others(9): Show |
3 | a0001c0001t0003g0129a0001c0001t0003g0155a0001c0001t0003g0156 | 3 | HG02559.hp1 HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.224+28145_224+2816 others(20): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49582952 | |||||
| chr3:49582952
|
CATTT | C | 4 | a0005c0007t0007g0002a0005c0007t0034g0004a0005c0034t0015g0001others(1): Show | 4 | HG02451.hp2 HG02683.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+28157_224+2816 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49582952 | |||||
| chr3:49583293
|
G | A | 185 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.224+28467G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49583293 | ||||||
| chr3:49583337
|
A | G | 82 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.224+28511A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49583337 | ||||||
| chr3:49583615
|
AAATAAAA others(12): Show |
A | 1 | a0003c0003t0004g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.224+28792_224+2881 others(23): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49583615 | |||||
| chr3:49583753
|
G | A | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+28927G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49583753 | ||||||
| chr3:49583864
|
G | GATTT | 4 | a0005c0007t0033g0005a0005c0007t0034g0004a0005c0034t0015g0001others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+29061_224+2906 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49583864 | |||||
| chr3:49583934
|
C | T | 17 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(14): Show | 17 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.224+29108C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49583934 | ||||||
| chr3:49583979
|
T | C | 1 | a0003c0004t0004g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.224+29153T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49583979 | ||||||
| chr3:49584087
|
G | A | 3 | a0003c0004t0004g0024a0003c0004t0004g0026a0003c0033t0004g0025 | 3 | HG01069.hp2 HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.224+29261G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584087 | ||||||
| chr3:49584121
|
G | A | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+29295G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584121 | ||||||
| chr3:49584285
|
A | AT | 166 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.224+29469dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49584285 | |||||
| chr3:49584285
|
A | ATT | 5 | a0001c0001t0002g0131a0001c0001t0002g0139a0002c0002t0001g0087others(2): Show | 5 | HG00099.hp1 HG00140.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.224+29468_224+2946 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49584285 | |||||
| chr3:49584384
|
T | G | 2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.224+29558T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584384 | ||||||
| chr3:49584561
|
C | T | 149 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.224+29735C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584561 | ||||||
| chr3:49584691
|
C | T | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+29865C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584691 | ||||||
| chr3:49584698
|
T | C | 1 | a0001c0001t0026g0146 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.224+29872T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584698 | ||||||
| chr3:49584716
|
G | A | 3 | a0002c0002t0001g0081a0002c0002t0001g0082a0002c0002t0001g0083 | 3 | HG00323.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.224+29890G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584716 | ||||||
| chr3:49584992
|
A | G | 1 | a0001c0001t0011g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.224+30166A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584992 | ||||||
| chr3:49585116
|
T | G | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.224+30290T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49585116 | ||||||
| chr3:49585199
|
G | GT | 156 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.224+30383dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49585199 | |||||
| chr3:49585237
|
T | C | 1 | a0005c0007t0007g0002 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.224+30411T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49585237 | ||||||
| chr3:49585439
|
G | A | 8 | a0001c0001t0002g0161a0006c0005t0008g0064a0006c0005t0008g0068others(5): Show | 8 | HG00544.hp2 HG02735.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.224+30613G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49585439 | ||||||
| chr3:49585565
|
C | T | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+30739C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49585565 | ||||||
| chr3:49585700
|
CTAAT | C | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG01257.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.224+30876_224+3087 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49585700 | |||||
| chr3:49585880
|
G | A | 1 | a0008c0015t0002g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.224+31054G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49585880 | ||||||
| chr3:49586013
|
A | G | 7 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.224+31187A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586013 | ||||||
| chr3:49586076
|
C | G | 1 | a0001c0001t0003g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.224+31250C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586076 | ||||||
| chr3:49586130
|
T | C | 1 | a0022c0024t0007g0008 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.224+31304T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586130 | ||||||
| chr3:49586251
|
G | C | 4 | a0001c0001t0009g0094a0001c0001t0009g0149a0009c0014t0009g0042others(1): Show | 4 | HG01081.hp2 HG01192.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+31425G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586251 | ||||||
| chr3:49586326
|
C | CTCTA | 64 | a0001c0001t0002g0095a0001c0001t0002g0105a0001c0001t0002g0107others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.224+31535_224+3153 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49586326 | |||||
| chr3:49586326
|
C | CTCTATCT others(1): Show |
57 | a0001c0001t0002g0097a0001c0001t0002g0102a0001c0001t0002g0110others(54): Show | 57 | HG00140.hp1 HG01081.hp2 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.224+31531_224+3153 others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49586326 | |||||
| chr3:49586326
|
C | CTCTATCT others(5): Show |
8 | a0001c0001t0002g0113a0001c0001t0002g0140a0001c0001t0003g0159others(5): Show | 8 | HG02735.hp2 HG02976.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+31527_224+3153 others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49586326 | |||||
| chr3:49586326
|
C | CTCTATCT others(9): Show |
4 | a0002c0002t0001g0089a0002c0002t0001g0184a0002c0002t0001g0185others(1): Show | 4 | HG02970.hp2 HG03710.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+31523_224+3153 others(20): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49586326 | |||||
| chr3:49586326
|
CTCTA | C | 4 | a0001c0001t0009g0149a0001c0001t0031g0142a0002c0020t0024g0166others(1): Show | 4 | HG01109.hp1 HG01928.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+31535_224+3153 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49586326 | |||||
| chr3:49586583
|
C | T | 2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.224+31757C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586583 | ||||||
| chr3:49586632
|
T | C | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.224+31806T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586632 | ||||||
| chr3:49586662
|
T | G | 172 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.224+31836T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586662 | ||||||
| chr3:49586944
|
A | C | 62 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.224+32118A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586944 | ||||||
| chr3:49586982
|
G | A | 1 | a0017c0038t0027g0003 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.224+32156G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586982 | ||||||
| chr3:49587219
|
G | A | 14 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0016others(11): Show | 14 | HG01074.hp2 HG01884.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.224+32393G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49587219 | ||||||
| chr3:49587376
|
C | T | 1 | a0022c0024t0007g0008 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.224+32550C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49587376 | ||||||
| chr3:49587660
|
G | C | 7 | a0003c0003t0004g0014a0003c0003t0004g0016a0003c0003t0004g0017others(4): Show | 7 | HG01074.hp2 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.224+32834G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49587660 | ||||||
| chr3:49587887
|
T | TTTTCTTT others(17): Show |
1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+33064_224+3306 others(28): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | |||||
| chr3:49587887
|
T | TTTTTC | 21 | a0001c0001t0007g0043a0001c0001t0018g0109a0001c0016t0003g0164others(18): Show | 21 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.224+33101_224+3310 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | |||||
| chr3:49587887
|
T | TTTTTCTT others(3): Show |
33 | a0001c0001t0002g0113a0001c0001t0002g0151a0001c0001t0002g0177others(30): Show | 33 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.224+33096_224+3310 others(14): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | |||||
| chr3:49587887
|
T | TTTTTCTT others(8): Show |
34 | a0001c0001t0002g0095a0001c0001t0002g0104a0001c0001t0002g0107others(31): Show | 34 | HG00323.hp2 HG01074.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.224+33091_224+3310 others(19): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | |||||
| chr3:49587887
|
T | TTTTTCTT others(13): Show |
31 | a0001c0001t0002g0097a0001c0001t0002g0105a0001c0001t0002g0115others(28): Show | 31 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.224+33086_224+3310 others(24): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | |||||
| chr3:49587887
|
T | TTTTTCTT others(18): Show |
27 | a0001c0001t0002g0110a0001c0001t0002g0131a0001c0001t0002g0133others(24): Show | 27 | HG00544.hp1 HG00642.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.224+33081_224+3310 others(29): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | |||||
| chr3:49587887
|
T | TTTTTCTT others(23): Show |
11 | a0001c0001t0003g0041a0001c0001t0003g0122a0001c0001t0003g0126others(8): Show | 11 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.224+33076_224+3310 others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | |||||
| chr3:49587887
|
T | TTTTTCTT others(28): Show |
1 | a0002c0019t0001g0056 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.224+33071_224+3310 others(39): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | |||||
| chr3:49587887
|
TTTTTC | T | 11 | a0002c0002t0001g0152a0002c0002t0001g0180a0002c0002t0001g0181others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.224+33101_224+3310 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | |||||
| chr3:49587887
|
TTTTTCTT others(3): Show |
T | 6 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(3): Show | 6 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.224+33096_224+3310 others(14): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | |||||
| chr3:49587887
|
TTTTTCTT others(13): Show |
T | 2 | a0001c0001t0003g0159a0001c0001t0029g0158 | 2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.224+33086_224+3310 others(24): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | |||||
| chr3:49587928
|
T | TTTTCTTT others(22): Show |
1 | a0001c0001t0019g0093 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.224+33105_224+3310 others(33): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587928 | |||||
| chr3:49588218
|
G | A | 1 | a0002c0002t0017g0058 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.224+33392G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49588218 | ||||||
| chr3:49588500
|
A | C | 3 | a0002c0002t0001g0081a0002c0002t0001g0082a0002c0002t0001g0083 | 3 | HG00323.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.224+33674A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49588500 | ||||||
| chr3:49588703
|
G | T | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+33877G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49588703 | ||||||
| chr3:49588749
|
T | G | 76 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.224+33923T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49588749 | ||||||
| chr3:49588873
|
G | A | 172 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.224+34047G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49588873 | ||||||
| chr3:49588919
|
G | GT | 7 | a0001c0001t0002g0133a0001c0001t0030g0121a0003c0004t0004g0015others(4): Show | 7 | HG00544.hp2 HG00642.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.224+34106dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49588919 | |||||
| chr3:49589040
|
G | A | 1 | a0001c0001t0020g0092 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.224+34214G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49589040 | ||||||
| chr3:49589082
|
A | ATTTTTT | 87 | a0001c0001t0002g0095a0001c0001t0002g0102a0001c0001t0002g0104others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.224+34265_224+3427 others(10): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49589082 | |||||
| chr3:49589082
|
A | ATTTTTTT | 58 | a0001c0001t0002g0097a0001c0001t0002g0131a0001c0001t0002g0151others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.224+34264_224+3427 others(11): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49589082 | |||||
| chr3:49589082
|
A | ATTTTTTT others(1): Show |
10 | a0002c0002t0001g0053a0002c0002t0001g0061a0002c0002t0001g0078others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.224+34263_224+3427 others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49589082 | |||||
| chr3:49589167
|
C | T | 13 | a0001c0016t0003g0164a0002c0002t0001g0088a0002c0002t0001g0089others(10): Show | 13 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.224+34341C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49589167 | ||||||
| chr3:49589211
|
C | T | 4 | a0001c0001t0002g0161a0011c0010t0001g0065a0012c0011t0001g0066others(1): Show | 4 | HG00544.hp2 HG02735.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+34385C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49589211 | ||||||
| chr3:49589233
|
C | T | 13 | a0001c0016t0003g0164a0002c0002t0001g0088a0002c0002t0001g0089others(10): Show | 13 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.224+34407C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49589233 | ||||||
| chr3:49589479
|
C | T | 1 | a0005c0007t0033g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.224+34653C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49589479 | ||||||
| chr3:49589513
|
C | CT | 183 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.224+34698dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49589513 | |||||
| chr3:49589646
|
A | G | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0024c0029t0003g0049 | 3 | HG02258.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.224+34820A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49589646 | ||||||
| chr3:49589844
|
G | GT | 69 | a0001c0001t0002g0161a0001c0001t0003g0153a0001c0001t0003g0154others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.224+35030dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49589844 | |||||
| chr3:49590027
|
G | A | 2 | a0002c0002t0001g0081a0002c0002t0001g0083 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.225-34948G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590027 | ||||||
| chr3:49590106
|
G | C | 1 | a0017c0038t0027g0003 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.225-34869G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590106 | ||||||
| chr3:49590135
|
C | T | 1 | a0001c0001t0002g0151 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225-34840C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590135 | ||||||
| chr3:49590327
|
AAAAC | A | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-34644_225-3464 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49590327 | |||||
| chr3:49590420
|
G | C | 2 | a0001c0001t0002g0176a0001c0001t0002g0178 | 2 | HG02004.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.225-34555G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590420 | ||||||
| chr3:49590564
|
C | A | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-34411C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590564 | ||||||
| chr3:49590714
|
C | T | 1 | a0001c0001t0003g0130 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.225-34261C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590714 | ||||||
| chr3:49590722
|
CATA | C | 11 | a0003c0004t0004g0024a0003c0004t0004g0026a0003c0004t0004g0027others(8): Show | 11 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.225-34247_225-3424 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49590722 | |||||
| chr3:49590767
|
A | T | 1 | a0002c0002t0001g0076 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.225-34208A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590767 | ||||||
| chr3:49591373
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.225-33602C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49591373 | ||||||
| chr3:49591588
|
ATTTTTG | A | 3 | a0002c0002t0001g0081a0002c0002t0001g0082a0002c0002t0001g0083 | 3 | HG00323.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.225-33369_225-3336 others(10): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49591588 | |||||
| chr3:49591605
|
T | G | 1 | a0001c0001t0002g0161 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.225-33370T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49591605 | ||||||
| chr3:49591606
|
G | T | 1 | a0001c0001t0002g0161 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.225-33369G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49591606 | ||||||
| chr3:49591958
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0002c0018t0001g0009others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-33017G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49591958 | ||||||
| chr3:49592122
|
A | T | 1 | a0001c0001t0007g0006 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.225-32853A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592122 | ||||||
| chr3:49592202
|
C | T | 4 | a0001c0001t0002g0161a0011c0010t0001g0065a0012c0011t0001g0066others(1): Show | 4 | HG00544.hp2 HG02735.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-32773C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592202 | ||||||
| chr3:49592256
|
C | G | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0002c0018t0001g0009 | 3 | HG02257.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.225-32719C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592256 | ||||||
| chr3:49592340
|
C | A | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.225-32635C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592340 | ||||||
| chr3:49592476
|
G | A | 1 | a0001c0016t0003g0164 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.225-32499G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592476 | ||||||
| chr3:49592510
|
T | C | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0043others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-32465T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592510 | ||||||
| chr3:49592645
|
G | T | 1 | a0003c0003t0004g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225-32330G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592645 | ||||||
| chr3:49593733
|
T | C | 1 | a0001c0001t0002g0161 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.225-31242T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593733 | ||||||
| chr3:49593734
|
C | T | 1 | a0001c0001t0002g0161 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.225-31241C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593734 | ||||||
| chr3:49593788
|
G | T | 59 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.225-31187G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593788 | ||||||
| chr3:49593805
|
G | GT | 7 | a0001c0001t0002g0102a0001c0001t0002g0135a0001c0001t0002g0147others(4): Show | 7 | HG01884.hp2 HG01934.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-31155dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49593805 | |||||
| chr3:49593812
|
T | G | 1 | a0003c0003t0004g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.225-31163T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593812 | ||||||
| chr3:49593893
|
C | T | 73 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.225-31082C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593893 | ||||||
| chr3:49593903
|
C | T | 1 | a0022c0024t0007g0008 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.225-31072C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593903 | ||||||
| chr3:49593960
|
G | A | 17 | a0001c0001t0002g0095a0001c0001t0002g0105a0001c0001t0002g0107others(14): Show | 17 | HG00544.hp1 HG00735.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.225-31015G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593960 | ||||||
| chr3:49594152
|
G | A | 13 | a0001c0016t0003g0164a0002c0002t0001g0088a0002c0002t0001g0089others(10): Show | 13 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.225-30823G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594152 | ||||||
| chr3:49594227
|
G | A | 2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-30748G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594227 | ||||||
| chr3:49594236
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.225-30739G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594236 | ||||||
| chr3:49594257
|
A | G | 1 | a0003c0003t0004g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.225-30718A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594257 | ||||||
| chr3:49594521
|
C | T | 1 | a0002c0002t0001g0090 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.225-30454C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594521 | ||||||
| chr3:49594876
|
G | A | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.225-30099G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594876 | ||||||
| chr3:49594883
|
T | A | 1 | a0003c0003t0014g0160 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225-30092T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594883 | ||||||
| chr3:49594890
|
A | AT | 148 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.225-30070dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49594890 | |||||
| chr3:49595089
|
C | A | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-29886C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49595089 | ||||||
| chr3:49595192
|
A | AT | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.225-29766dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49595192 | |||||
| chr3:49595194
|
T | TC | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-29781_225-2978 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49595194 | ||||||
| chr3:49595195
|
T | C | 145 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.225-29780T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49595195 | ||||||
| chr3:49596239
|
C | T | 1 | a0001c0001t0032g0144 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.225-28736C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49596239 | ||||||
| chr3:49596670
|
A | G | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-28305A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49596670 | ||||||
| chr3:49596679
|
C | G | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0024c0029t0003g0049 | 3 | HG02258.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.225-28296C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49596679 | ||||||
| chr3:49597161
|
T | C | 7 | a0002c0002t0005g0039a0002c0002t0005g0062a0002c0002t0005g0074others(4): Show | 7 | HG01081.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-27814T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597161 | ||||||
| chr3:49597263
|
G | A | 61 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.225-27712G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597263 | ||||||
| chr3:49597273
|
C | T | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-27702C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597273 | ||||||
| chr3:49597402
|
C | T | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0024c0029t0003g0049 | 3 | HG02258.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.225-27573C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597402 | ||||||
| chr3:49597435
|
A | G | 1 | a0001c0001t0003g0048 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.225-27540A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597435 | ||||||
| chr3:49597601
|
G | C | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225-27374G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597601 | ||||||
| chr3:49597921
|
G | A | 60 | a0001c0001t0002g0161a0001c0001t0012g0057a0001c0016t0003g0164others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.225-27054G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597921 | ||||||
| chr3:49597923
|
G | A | 1 | a0003c0003t0004g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225-27052G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597923 | ||||||
| chr3:49597923
|
G | C | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-27052G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597923 | ||||||
| chr3:49598114
|
A | T | 2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-26861A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49598114 | ||||||
| chr3:49598512
|
C | T | 1 | a0001c0001t0002g0113 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.225-26463C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49598512 | ||||||
| chr3:49598801
|
G | C | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225-26174G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49598801 | ||||||
| chr3:49599468
|
G | A | 3 | a0002c0002t0001g0170a0002c0002t0001g0174a0002c0002t0001g0175 | 3 | HG01515.hp1 HG01517.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.225-25507G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49599468 | ||||||
| chr3:49599544
|
G | C | 1 | a0001c0001t0002g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.225-25431G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49599544 | ||||||
| chr3:49599616
|
C | G | 4 | a0001c0001t0011g0098a0001c0001t0011g0125a0001c0001t0011g0127others(1): Show | 4 | HG00323.hp2 HG01106.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-25359C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49599616 | ||||||
| chr3:49599666
|
A | C | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.225-25309A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49599666 | ||||||
| chr3:49599951
|
G | A | 8 | a0001c0001t0002g0161a0006c0005t0008g0064a0006c0005t0008g0068others(5): Show | 8 | HG00544.hp2 HG02735.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.225-25024G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49599951 | ||||||
| chr3:49600067
|
G | C | 2 | a0001c0001t0002g0161a0003c0003t0004g0046 | 2 | NA18906.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.225-24908G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49600067 | ||||||
| chr3:49600068
|
C | G | 1 | a0001c0001t0002g0161 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.225-24907C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49600068 | ||||||
| chr3:49600609
|
C | T | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0002c0018t0001g0009 | 3 | HG02257.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.225-24366C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49600609 | ||||||
| chr3:49600651
|
AAAATT | A | 64 | a0001c0001t0002g0161a0001c0001t0007g0006a0001c0001t0007g0007others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.225-24322_225-2431 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49600651 | |||||
| chr3:49600667
|
G | T | 1 | a0003c0003t0004g0022 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.225-24308G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49600667 | ||||||
| chr3:49601380
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.225-23595G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49601380 | ||||||
| chr3:49601689
|
T | G | 2 | a0001c0001t0007g0006a0001c0001t0007g0007 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.225-23286T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49601689 | ||||||
| chr3:49601927
|
A | G | 1 | a0002c0002t0001g0152 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.225-23048A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49601927 | ||||||
| chr3:49602020
|
A | T | 2 | a0002c0002t0001g0063a0002c0002t0001g0070 | 2 | HG01167.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.225-22955A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602020 | ||||||
| chr3:49602102
|
T | C | 2 | a0002c0002t0001g0088a0002c0002t0001g0090 | 2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-22873T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602102 | ||||||
| chr3:49602173
|
G | C | 2 | a0001c0001t0012g0116a0001c0001t0012g0136 | 2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.225-22802G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602173 | ||||||
| chr3:49602370
|
G | T | 155 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.225-22605G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602370 | ||||||
| chr3:49602377
|
G | T | 1 | a0003c0003t0004g0014 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.225-22598G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602377 | ||||||
| chr3:49602442
|
T | A | 1 | a0001c0001t0007g0043 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.225-22533T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602442 | ||||||
| chr3:49602445
|
A | AT | 6 | a0001c0001t0020g0092a0001c0001t0032g0144a0001c0027t0003g0186others(3): Show | 6 | HG00544.hp1 HG01167.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-22511dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49602445 | |||||
| chr3:49602445
|
A | T | 1 | a0001c0001t0007g0043 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.225-22530A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602445 | ||||||
| chr3:49602445
|
AT | A | 11 | a0001c0001t0003g0128a0002c0002t0001g0063a0002c0002t0001g0090others(8): Show | 11 | HG00639.hp1 HG01109.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.225-22511delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49602445 | |||||
| chr3:49602532
|
G | A | 1 | a0017c0038t0027g0003 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.225-22443G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602532 | ||||||
| chr3:49602780
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.225-22195C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602780 | ||||||
| chr3:49602941
|
G | A | 3 | a0001c0001t0002g0102a0001c0001t0002g0114a0001c0001t0002g0135 | 3 | HG02055.hp1 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.225-22034G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602941 | ||||||
| chr3:49602994
|
C | T | 3 | a0001c0001t0002g0115a0001c0001t0002g0133a0001c0001t0002g0141 | 3 | HG00642.hp2 HG01168.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.225-21981C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602994 | ||||||
| chr3:49603114
|
GGGCCCCT others(22): Show |
G | 6 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(3): Show | 6 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-21849_225-2182 others(33): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49603114 | |||||
| chr3:49603160
|
C | T | 2 | a0001c0001t0002g0147a0001c0001t0021g0145 | 2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.225-21815C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49603160 | ||||||
| chr3:49603616
|
G | A | 7 | a0002c0002t0005g0039a0002c0002t0005g0062a0002c0002t0005g0074others(4): Show | 7 | HG01081.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-21359G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49603616 | ||||||
| chr3:49604594
|
C | T | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.225-20381C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604594 | ||||||
| chr3:49604643
|
G | A | 2 | a0001c0001t0012g0116a0001c0001t0012g0136 | 2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.225-20332G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604643 | ||||||
| chr3:49604703
|
C | G | 1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-20272C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604703 | ||||||
| chr3:49604704
|
A | C | 1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-20271A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604704 | ||||||
| chr3:49604705
|
G | A | 1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-20270G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604705 | ||||||
| chr3:49604944
|
T | C | 1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-20031T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604944 | ||||||
| chr3:49604997
|
C | T | 61 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.225-19978C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604997 | ||||||
| chr3:49605264
|
T | A | 1 | a0002c0002t0001g0076 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.225-19711T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605264 | ||||||
| chr3:49605303
|
A | C | 1 | a0001c0001t0011g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-19672A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605303 | ||||||
| chr3:49605307
|
A | T | 1 | a0002c0002t0001g0182 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-19668A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605307 | ||||||
| chr3:49605308
|
T | A | 1 | a0002c0002t0001g0182 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-19667T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605308 | ||||||
| chr3:49605313
|
TTA | T | 14 | a0001c0001t0003g0047a0001c0001t0003g0048a0002c0002t0001g0170others(11): Show | 14 | HG01515.hp1 HG01517.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.225-19650_225-1964 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605313 | |||||
| chr3:49605327
|
T | A | 1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-19648T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605327 | ||||||
| chr3:49605405
|
T | A | 1 | a0003c0003t0004g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225-19570T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605405 | ||||||
| chr3:49605436
|
TATTATAT others(113): Show |
T | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19536_225-1941 others(4): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605436 | |||||
| chr3:49605439
|
T | TATATATA others(23): Show |
3 | a0003c0003t0010g0010a0003c0003t0010g0011a0003c0003t0010g0012 | 3 | HG02622.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.225-19483_225-1945 others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605439 | |||||
| chr3:49605439
|
TATATATA others(23): Show |
T | 1 | a0003c0003t0004g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225-19483_225-1945 others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605439 | |||||
| chr3:49605447
|
T | A | 63 | a0001c0001t0012g0057a0001c0001t0029g0158a0001c0017t0002g0106others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.225-19528T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605447 | ||||||
| chr3:49605454
|
A | T | 2 | a0001c0001t0029g0158a0001c0017t0002g0106 | 2 | HG06807.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.225-19521A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605454 | ||||||
| chr3:49605461
|
TTA | T | 2 | a0003c0003t0014g0160a0003c0023t0014g0157 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-19507_225-1950 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605461 | |||||
| chr3:49605469
|
A | T | 58 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.225-19506A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605469 | ||||||
| chr3:49605476
|
A | ATTATATA others(87): Show |
1 | a0001c0001t0003g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.225-19492_225-1949 others(98): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605476 | |||||
| chr3:49605477
|
T | A | 4 | a0011c0010t0001g0065a0011c0010t0001g0165a0012c0011t0001g0066others(1): Show | 4 | HG00544.hp2 HG02735.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-19498T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605477 | ||||||
| chr3:49605477
|
T | TTATATAA others(39): Show |
8 | a0003c0003t0004g0014a0003c0003t0004g0016a0003c0003t0004g0017others(5): Show | 8 | HG01074.hp2 HG01884.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.225-19454_225-1945 others(50): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605477 | |||||
| chr3:49605477
|
T | TTATATAT others(39): Show |
1 | a0003c0003t0004g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.225-19492_225-1949 others(50): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605477 | |||||
| chr3:49605477
|
T | TTATATAT others(64): Show |
1 | a0001c0001t0002g0139 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.225-19492_225-1949 others(75): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605477 | |||||
| chr3:49605479
|
A | ATATAATA others(31): Show |
1 | a0003c0004t0004g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.225-19484_225-1948 others(42): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605479 | |||||
| chr3:49605484
|
A | T | 84 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.225-19491A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605484 | ||||||
| chr3:49605491
|
T | A | 1 | a0001c0017t0002g0106 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.225-19484T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605491 | ||||||
| chr3:49605491
|
T | TTATATAT others(4): Show |
1 | a0003c0003t0014g0160 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225-19477_225-1947 others(15): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605491 | |||||
| chr3:49605492
|
T | A | 80 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.225-19483T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605492 | ||||||
| chr3:49605493
|
ATATATAA others(7): Show |
A | 1 | a0003c0023t0014g0157 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.225-19467_225-1945 others(18): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605493 | |||||
| chr3:49605499
|
A | T | 3 | a0011c0010t0001g0065a0011c0010t0001g0165a0012c0011t0001g0066 | 3 | HG02735.hp1 NA18963.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.225-19476A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605499 | ||||||
| chr3:49605500
|
A | T | 79 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.225-19475A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605500 | ||||||
| chr3:49605507
|
T | A | 3 | a0001c0017t0002g0106a0002c0002t0001g0071a0012c0011t0001g0067 | 3 | HG00544.hp2 HG02615.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.225-19468T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605507 | ||||||
| chr3:49605513
|
A | ATATTTTA others(24): Show |
2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-19462_225-1946 others(35): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605513 | ||||||
| chr3:49605513
|
A | T | 1 | a0003c0023t0014g0157 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.225-19462A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605513 | ||||||
| chr3:49605513
|
AAT | A | 130 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.225-19452_225-1945 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605513 | |||||
| chr3:49605513
|
AATATAT | A | 4 | a0006c0005t0008g0064a0006c0005t0008g0068a0006c0005t0008g0069others(1): Show | 4 | NA18951.hp2 NA19000.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-19456_225-1945 others(10): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605513 | |||||
| chr3:49605514
|
A | T | 10 | a0001c0001t0002g0139a0001c0001t0007g0006a0001c0001t0007g0007others(7): Show | 10 | HG00544.hp2 HG01074.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.225-19461A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605514 | ||||||
| chr3:49605515
|
T | TA | 2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-19459dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605515 | |||||
| chr3:49605515
|
T | TATATA | 6 | a0001c0001t0002g0139a0001c0001t0007g0006a0001c0001t0007g0007others(3): Show | 6 | HG01074.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-19459_225-1945 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605515 | |||||
| chr3:49605516
|
A | ATATAT | 2 | a0002c0002t0001g0071a0012c0011t0001g0067 | 2 | HG00544.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.225-19458_225-1945 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605516 | |||||
| chr3:49605516
|
A | ATATATAA others(90): Show |
1 | a0001c0001t0003g0096 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.225-19453_225-1945 others(101): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605516 | |||||
| chr3:49605516
|
A | T | 1 | a0001c0001t0003g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.225-19459A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605516 | ||||||
| chr3:49605518
|
A | AATATATA others(12): Show |
1 | a0001c0001t0002g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.225-19457_225-1945 others(23): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605518 | ||||||
| chr3:49605524
|
A | AT | 2 | a0001c0001t0002g0151a0002c0020t0024g0166 | 2 | HG02723.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.225-19451_225-1945 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605524 | ||||||
| chr3:49605524
|
A | T | 5 | a0007c0013t0013g0050a0007c0013t0013g0051a0011c0010t0001g0065others(2): Show | 5 | HG02572.hp2 HG02735.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19451A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605524 | ||||||
| chr3:49605525
|
A | T | 2 | a0002c0002t0001g0071a0012c0011t0001g0067 | 2 | HG00544.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.225-19450A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605525 | ||||||
| chr3:49605531
|
A | T | 2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-19444A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605531 | ||||||
| chr3:49605532
|
A | T | 3 | a0001c0001t0002g0140a0001c0001t0003g0096a0001c0017t0002g0106 | 3 | HG03942.hp1 HG04228.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.225-19443A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605532 | ||||||
| chr3:49605539
|
TTA | T | 64 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0153others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.225-19428_225-1942 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605539 | |||||
| chr3:49605540
|
T | TATATATA others(26): Show |
1 | a0012c0011t0001g0067 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.225-19428_225-1942 others(37): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605540 | |||||
| chr3:49605544
|
T | TA | 3 | a0011c0010t0001g0065a0011c0010t0001g0165a0012c0011t0001g0066 | 3 | HG02735.hp1 NA18963.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.225-19430dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605544 | |||||
| chr3:49605545
|
A | AT | 2 | a0001c0001t0012g0116a0001c0001t0012g0136 | 2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.225-19429dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605545 | |||||
| chr3:49605547
|
AT | A | 14 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0016others(11): Show | 14 | HG01074.hp2 HG01884.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.225-19424delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605547 | |||||
| chr3:49605549
|
T | A | 6 | a0001c0001t0012g0116a0001c0001t0012g0136a0002c0002t0001g0071others(3): Show | 6 | HG00280.hp1 HG01515.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-19426T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605549 | ||||||
| chr3:49605550
|
T | A | 7 | a0001c0001t0002g0140a0001c0017t0002g0106a0011c0010t0001g0065others(4): Show | 7 | HG00544.hp2 HG02683.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-19425T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605550 | ||||||
| chr3:49605550
|
T | TA | 4 | a0001c0001t0003g0096a0001c0001t0003g0120a0007c0013t0013g0050others(1): Show | 4 | HG02572.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-19425_225-1942 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605550 | ||||||
| chr3:49605551
|
T | A | 2 | a0001c0001t0012g0116a0001c0001t0012g0136 | 2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.225-19424T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605551 | ||||||
| chr3:49605556
|
A | ATTT | 2 | a0001c0001t0002g0140a0001c0017t0002g0106 | 2 | HG03942.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.225-19419_225-1941 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605556 | ||||||
| chr3:49605556
|
A | T | 1 | a0012c0011t0001g0067 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.225-19419A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605556 | ||||||
| chr3:49605557
|
A | T | 1 | a0012c0011t0001g0067 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.225-19418A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605557 | ||||||
| chr3:49605558
|
T | C | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19417T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605558 | ||||||
| chr3:49605564
|
T | A | 3 | a0001c0001t0002g0140a0001c0017t0002g0106a0012c0011t0001g0067 | 3 | HG00544.hp2 HG03942.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.225-19411T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605564 | ||||||
| chr3:49605564
|
T | TAATATAT others(127): Show |
4 | a0001c0001t0003g0041a0001c0001t0003g0122a0001c0001t0003g0128others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-19411_225-1941 others(138): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605564 | ||||||
| chr3:49605564
|
T | TAATATAT others(25): Show |
1 | a0002c0002t0001g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.225-19411_225-1941 others(36): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605564 | ||||||
| chr3:49605565
|
T | A | 2 | a0001c0001t0003g0138a0001c0001t0031g0142 | 2 | HG01109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.225-19410T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605565 | ||||||
| chr3:49605569
|
TA | T | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19405delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605569 | ||||||
| chr3:49605571
|
T | G | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19404T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605571 | ||||||
| chr3:49605571
|
T | TA | 2 | a0001c0001t0002g0113a0001c0001t0002g0151 | 2 | NA18973.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.225-19404_225-1940 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605571 | ||||||
| chr3:49605571
|
T | TTA | 6 | a0003c0003t0004g0016a0003c0003t0004g0017a0003c0003t0004g0018others(3): Show | 6 | HG01074.hp2 HG02965.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-19396_225-1939 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605571 | |||||
| chr3:49605572
|
T | A | 2 | a0001c0001t0003g0138a0001c0001t0031g0142 | 2 | HG01109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.225-19403T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605572 | ||||||
| chr3:49605572
|
T | TTTATATA | 3 | a0011c0010t0001g0065a0011c0010t0001g0165a0012c0011t0001g0066 | 3 | HG02735.hp1 NA18963.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.225-19403_225-1940 others(11): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605572 | ||||||
| chr3:49605573
|
ATATATAT | A | 54 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(51): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.225-19393_225-1938 others(11): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605573 | |||||
| chr3:49605579
|
A | T | 6 | a0001c0001t0003g0041a0001c0001t0003g0122a0001c0001t0003g0128others(3): Show | 6 | HG00544.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-19396A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605579 | ||||||
| chr3:49605580
|
T | A | 13 | a0001c0001t0002g0140a0001c0001t0003g0041a0001c0001t0003g0122others(10): Show | 13 | HG00544.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.225-19395T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605580 | ||||||
| chr3:49605580
|
T | TTA | 38 | a0001c0001t0002g0102a0001c0001t0002g0105a0001c0001t0002g0107others(35): Show | 38 | HG00544.hp1 HG00639.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.225-19389_225-1938 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | |||||
| chr3:49605580
|
T | TTATATAT others(94): Show |
27 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0104others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.225-19388_225-1938 others(105): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | |||||
| chr3:49605580
|
T | TTATATAT others(127): Show |
2 | a0001c0001t0002g0110a0001c0001t0002g0133 | 2 | HG00642.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.225-19388_225-1938 others(138): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | |||||
| chr3:49605580
|
T | TTATATAT others(61): Show |
1 | a0022c0024t0007g0008 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.225-19388_225-1938 others(72): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | |||||
| chr3:49605580
|
T | TTATATAT others(94): Show |
7 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(4): Show | 7 | HG00323.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-19388_225-1938 others(105): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | |||||
| chr3:49605580
|
T | TTATATAT others(127): Show |
2 | a0001c0001t0007g0006a0001c0001t0007g0007 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.225-19388_225-1938 others(138): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | |||||
| chr3:49605580
|
T | TTATATAT others(159): Show |
2 | a0001c0001t0003g0047a0024c0029t0003g0049 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.225-19388_225-1938 others(170): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | |||||
| chr3:49605580
|
T | TTATATAT others(160): Show |
1 | a0001c0001t0003g0048 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.225-19388_225-1938 others(171): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | |||||
| chr3:49605580
|
T | TTATATAT others(92): Show |
1 | a0001c0001t0011g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-19388_225-1938 others(103): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | |||||
| chr3:49605580
|
T | TTATATAT others(2): Show |
3 | a0011c0010t0001g0065a0011c0010t0001g0165a0012c0011t0001g0066 | 3 | HG02735.hp1 NA18963.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.225-19387_225-1938 others(13): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | |||||
| chr3:49605580
|
T | TTATATAT others(68): Show |
1 | a0001c0001t0011g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.225-19387_225-1938 others(79): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | |||||
| chr3:49605580
|
T | TTTATATA others(19): Show |
3 | a0001c0001t0003g0096a0007c0013t0013g0050a0007c0013t0013g0051 | 3 | HG02572.hp2 HG02922.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.225-19394_225-1939 others(30): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | |||||
| chr3:49605580
|
T | TTTATATA others(52): Show |
1 | a0001c0001t0003g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.225-19394_225-1939 others(63): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | |||||
| chr3:49605585
|
T | C | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19390T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605585 | ||||||
| chr3:49605588
|
T | A | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19387T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605588 | ||||||
| chr3:49605589
|
T | A | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-19386T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605589 | ||||||
| chr3:49605591
|
T | C | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19384T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605591 | ||||||
| chr3:49605597
|
A | T | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19378A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605597 | ||||||
| chr3:49605602
|
TA | T | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19372delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605602 | ||||||
| chr3:49605603
|
A | G | 1 | a0002c0002t0001g0167 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.225-19372A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605603 | ||||||
| chr3:49605604
|
T | A | 4 | a0001c0001t0003g0138a0001c0001t0031g0142a0002c0002t0001g0088others(1): Show | 4 | HG01109.hp1 HG03139.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-19371T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605604 | ||||||
| chr3:49605604
|
T | G | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19371T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605604 | ||||||
| chr3:49605604
|
T | TTATATAT others(52): Show |
1 | a0017c0038t0027g0003 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.225-19356_225-1935 others(63): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605604 | |||||
| chr3:49605611
|
T | TAATATAT others(127): Show |
1 | a0004c0006t0002g0036 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.225-19364_225-1936 others(138): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605611 | ||||||
| chr3:49605612
|
T | A | 21 | a0001c0001t0002g0102a0001c0001t0002g0105a0001c0001t0002g0107others(18): Show | 21 | HG00544.hp1 HG01081.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.225-19363T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605612 | ||||||
| chr3:49605617
|
A | ATATTTAT others(95): Show |
3 | a0001c0001t0002g0140a0001c0001t0020g0092a0001c0017t0002g0106 | 3 | HG01928.hp1 HG03942.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.225-19356_225-1935 others(106): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | |||||
| chr3:49605617
|
A | ATATTTAT others(124): Show |
1 | a0001c0001t0032g0144 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.225-19356_225-1935 others(135): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | |||||
| chr3:49605617
|
A | ATATTTAT others(86): Show |
1 | a0001c0001t0026g0146 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.225-19356_225-1935 others(97): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | |||||
| chr3:49605617
|
A | ATATTTAT others(128): Show |
1 | a0001c0001t0003g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.225-19356_225-1935 others(139): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | |||||
| chr3:49605617
|
A | ATATTTAT others(128): Show |
27 | a0001c0001t0002g0102a0001c0001t0002g0105a0001c0001t0002g0107others(24): Show | 27 | HG01081.hp2 HG01167.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.225-19356_225-1935 others(139): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | |||||
| chr3:49605617
|
A | ATATTTAT others(194): Show |
1 | a0001c0001t0003g0138 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.225-19356_225-1935 others(205): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | |||||
| chr3:49605617
|
A | ATATTTAT others(159): Show |
1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-19356_225-1935 others(170): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | |||||
| chr3:49605620
|
A | C | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19355A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605620 | ||||||
| chr3:49605620
|
A | T | 36 | a0001c0001t0002g0102a0001c0001t0002g0105a0001c0001t0002g0107others(33): Show | 36 | HG00544.hp1 HG00639.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.225-19355A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605620 | ||||||
| chr3:49605626
|
AT | A | 4 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-19348delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605626 | ||||||
| chr3:49605633
|
TTAC | T | 4 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-19341_225-1933 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605633 | ||||||
| chr3:49605634
|
T | A | 4 | a0001c0001t0002g0140a0001c0001t0003g0126a0003c0004t0004g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-19341T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605634 | ||||||
| chr3:49605636
|
C | A | 38 | a0001c0001t0002g0102a0001c0001t0002g0105a0001c0001t0002g0107others(35): Show | 38 | HG00544.hp1 HG00639.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.225-19339C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605636 | ||||||
| chr3:49605636
|
C | CATATATG others(29): Show |
5 | a0001c0001t0002g0133a0004c0006t0002g0035a0004c0006t0002g0037others(2): Show | 5 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.225-19306_225-1930 others(40): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605636 | |||||
| chr3:49605636
|
C | CATATATG others(29): Show |
1 | a0001c0001t0003g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.225-19304_225-1930 others(40): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605636 | |||||
| chr3:49605637
|
A | G | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19338A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605637 | ||||||
| chr3:49605642
|
TG | T | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19332delG | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605642 | ||||||
| chr3:49605643
|
G | T | 9 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0153others(6): Show | 9 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.225-19332G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605643 | ||||||
| chr3:49605645
|
A | T | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19330A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605645 | ||||||
| chr3:49605652
|
ATTAT | A | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19322_225-1931 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605652 | ||||||
| chr3:49605658
|
TATA | T | 5 | a0003c0004t0006g0029a0003c0004t0006g0030a0003c0004t0006g0031others(2): Show | 5 | HG01516.hp1 HG01517.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19313_225-1931 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605658 | |||||
| chr3:49605660
|
T | A | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19315T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605660 | ||||||
| chr3:49605661
|
A | T | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19314A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605661 | ||||||
| chr3:49605663
|
T | C | 5 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19312T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605663 | ||||||
| chr3:49605670
|
T | A | 42 | a0001c0001t0002g0102a0001c0001t0002g0105a0001c0001t0002g0107others(39): Show | 42 | HG00140.hp1 HG00544.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.225-19305T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605670 | ||||||
| chr3:49605670
|
T | TAAATATA others(29): Show |
28 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0104others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.225-19304_225-1930 others(40): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605670 | |||||
| chr3:49605672
|
C | A | 149 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.225-19303C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605672 | ||||||
| chr3:49605672
|
C | CATATATG others(29): Show |
2 | a0001c0001t0002g0131a0001c0001t0011g0098 | 2 | HG02735.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.225-19296_225-1926 others(40): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605672 | |||||
| chr3:49605672
|
C | CATATATG others(65): Show |
2 | a0001c0001t0011g0125a0001c0001t0011g0127 | 2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.225-19270_225-1926 others(76): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605672 | |||||
| chr3:49605691
|
A | ATATATAA others(29): Show |
2 | a0003c0003t0014g0160a0003c0023t0014g0157 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-19270_225-1926 others(40): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605691 | |||||
| chr3:49605729
|
T | G | 1 | a0010c0009t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-19246T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605729 | ||||||
| chr3:49605740
|
AATAT | A | 59 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.225-19229_225-1922 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605740 | |||||
| chr3:49605767
|
A | T | 1 | a0001c0001t0002g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.225-19208A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605767 | ||||||
| chr3:49605785
|
AATATATA others(11): Show |
A | 1 | a0001c0001t0020g0092 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.225-19173_225-1915 others(22): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605785 | |||||
| chr3:49605869
|
T | A | 1 | a0002c0002t0001g0182 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-19106T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605869 | ||||||
| chr3:49605872
|
T | TTATATAT others(23): Show |
57 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(54): Show | 57 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.225-19078_225-1907 others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605872 | |||||
| chr3:49605872
|
T | TTATATAT others(24): Show |
1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-19078_225-1907 others(35): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605872 | |||||
| chr3:49605884
|
A | ATAAATAT others(25): Show |
1 | a0010c0009t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-19078_225-1907 others(36): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605884 | |||||
| chr3:49605898
|
G | A | 155 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.225-19077G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605898 | ||||||
| chr3:49605906
|
A | ATATAGAT others(22): Show |
1 | a0002c0002t0001g0182 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-19069_225-1906 others(33): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605906 | ||||||
| chr3:49605909
|
T | A | 1 | a0002c0002t0001g0182 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-19066T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605909 | ||||||
| chr3:49605912
|
A | T | 1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-19063A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605912 | ||||||
| chr3:49605913
|
T | C | 1 | a0001c0001t0020g0092 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.225-19062T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605913 | ||||||
| chr3:49605923
|
T | G | 1 | a0010c0009t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-19052T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605923 | ||||||
| chr3:49605925
|
T | TA | 100 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0043others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.225-19046dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605925 | |||||
| chr3:49605929
|
ATCT | A | 82 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.225-19045_225-1904 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605929 | ||||||
| chr3:49605932
|
T | A | 1 | a0001c0001t0011g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-19043T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605932 | ||||||
| chr3:49605935
|
T | C | 83 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.225-19040T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605935 | ||||||
| chr3:49605938
|
T | A | 1 | a0002c0002t0001g0182 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-19037T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605938 | ||||||
| chr3:49605939
|
A | G | 2 | a0002c0002t0001g0081a0002c0002t0001g0083 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.225-19036A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605939 | ||||||
| chr3:49606018
|
ATATATT | A | 2 | a0003c0003t0014g0160a0003c0023t0014g0157 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-18951_225-1894 others(10): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606018 | |||||
| chr3:49606019
|
T | A | 1 | a0002c0002t0001g0182 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-18956T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606019 | ||||||
| chr3:49606032
|
A | C | 1 | a0003c0004t0006g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.225-18943A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606032 | ||||||
| chr3:49606040
|
T | A | 1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-18935T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606040 | ||||||
| chr3:49606041
|
T | A | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-18934T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606041 | ||||||
| chr3:49606060
|
A | AATAATAA others(12): Show |
1 | a0001c0001t0011g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18912_225-1891 others(23): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606060 | |||||
| chr3:49606071
|
TA | T | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-18899delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606071 | |||||
| chr3:49606074
|
A | T | 1 | a0001c0001t0011g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18901A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606074 | ||||||
| chr3:49606082
|
A | T | 1 | a0001c0001t0011g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18893A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606082 | ||||||
| chr3:49606083
|
AT | A | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-18886delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606083 | |||||
| chr3:49606085
|
T | A | 1 | a0001c0001t0011g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18890T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606085 | ||||||
| chr3:49606087
|
T | A | 1 | a0001c0001t0011g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18888T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606087 | ||||||
| chr3:49606096
|
A | T | 1 | a0001c0001t0011g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18879A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606096 | ||||||
| chr3:49606097
|
A | T | 1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-18878A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606097 | ||||||
| chr3:49606098
|
C | T | 1 | a0001c0001t0011g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18877C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606098 | ||||||
| chr3:49606098
|
CATATA | C | 59 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.225-18871_225-1886 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606098 | |||||
| chr3:49606108
|
A | T | 1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-18867A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606108 | ||||||
| chr3:49606111
|
A | T | 1 | a0001c0001t0003g0132 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.225-18864A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606111 | ||||||
| chr3:49606118
|
C | A | 1 | a0001c0001t0011g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18857C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606118 | ||||||
| chr3:49606118
|
C | CGTATAAT others(26): Show |
1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-18852_225-1885 others(37): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606118 | |||||
| chr3:49606118
|
C | CGTATATA others(25): Show |
30 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0115others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.225-18841_225-1884 others(36): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606118 | |||||
| chr3:49606118
|
C | CGTATATA others(57): Show |
1 | a0001c0001t0007g0043 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.225-18841_225-1884 others(68): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606118 | |||||
| chr3:49606118
|
C | CGTATATA others(57): Show |
2 | a0001c0001t0007g0006a0001c0001t0007g0007 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.225-18841_225-1884 others(68): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606118 | |||||
| chr3:49606118
|
C | T | 3 | a0003c0003t0004g0013a0008c0015t0002g0103a0008c0015t0002g0108 | 3 | HG01891.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.225-18857C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606118 | ||||||
| chr3:49606119
|
G | C | 1 | a0001c0001t0011g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18856G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606119 | ||||||
| chr3:49606120
|
T | A | 1 | a0010c0009t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-18855T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606120 | ||||||
| chr3:49606121
|
A | T | 1 | a0010c0009t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-18854A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606121 | ||||||
| chr3:49606126
|
T | TTA | 14 | a0003c0003t0004g0014a0003c0003t0004g0016a0003c0003t0004g0017others(11): Show | 14 | HG01074.hp2 HG01884.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.225-18842_225-1884 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606126 | |||||
| chr3:49606133
|
T | A | 1 | a0010c0009t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-18842T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606133 | ||||||
| chr3:49606133
|
T | TAA | 117 | a0001c0001t0002g0102a0001c0001t0002g0104a0001c0001t0002g0105others(114): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.225-18841_225-1884 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606133 | |||||
| chr3:49606134
|
A | AAATATAT others(27): Show |
2 | a0001c0001t0003g0137a0001c0027t0003g0186 | 2 | HG01167.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.225-18841_225-1884 others(38): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606134 | ||||||
| chr3:49606135
|
C | T | 120 | a0001c0001t0002g0102a0001c0001t0002g0104a0001c0001t0002g0105others(117): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.225-18840C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606135 | ||||||
| chr3:49606148
|
T | C | 3 | a0003c0004t0004g0024a0003c0004t0004g0026a0003c0033t0004g0025 | 3 | HG01069.hp2 HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.225-18827T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606148 | ||||||
| chr3:49606150
|
T | C | 1 | a0003c0003t0004g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.225-18825T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606150 | ||||||
| chr3:49606163
|
T | G | 4 | a0006c0005t0008g0064a0006c0005t0008g0068a0006c0005t0008g0069others(1): Show | 4 | NA18951.hp2 NA19000.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-18812T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606163 | ||||||
| chr3:49606167
|
T | A | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-18808T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606167 | ||||||
| chr3:49606172
|
T | A | 1 | a0001c0001t0003g0122 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.225-18803T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606172 | ||||||
| chr3:49606179
|
GTA | G | 95 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0113others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.225-18788_225-1878 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606179 | |||||
| chr3:49606181
|
A | ATATATTA others(21): Show |
33 | a0001c0001t0002g0104a0001c0001t0002g0107a0001c0001t0002g0112others(30): Show | 33 | HG00544.hp1 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.225-18789_225-1878 others(32): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606181 | |||||
| chr3:49606181
|
A | ATATATTA others(136): Show |
1 | a0003c0003t0004g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225-18789_225-1878 others(147): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606181 | |||||
| chr3:49606181
|
A | ATATATTA others(51): Show |
6 | a0001c0001t0002g0102a0001c0001t0002g0105a0001c0001t0002g0110others(3): Show | 6 | HG02055.hp1 HG02258.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-18789_225-1878 others(62): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606181 | |||||
| chr3:49606181
|
A | ATATATTA others(81): Show |
3 | a0001c0001t0003g0119a0001c0001t0003g0123a0019c0026t0002g0100 | 3 | HG01074.hp1 HG01257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.225-18789_225-1878 others(92): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606181 | |||||
| chr3:49606187
|
A | T | 41 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(38): Show | 41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18788A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606187 | ||||||
| chr3:49606187
|
ATT | A | 2 | a0009c0014t0009g0042a0009c0014t0009g0099 | 2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.225-18787_225-1878 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606187 | ||||||
| chr3:49606188
|
T | A | 41 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(38): Show | 41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18787T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606188 | ||||||
| chr3:49606191
|
T | A | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-18784T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606191 | ||||||
| chr3:49606193
|
T | A | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-18782T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606193 | ||||||
| chr3:49606193
|
T | TA | 39 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(36): Show | 39 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.225-18781dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606193 | |||||
| chr3:49606195
|
T | A | 39 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(36): Show | 39 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.225-18780T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606195 | ||||||
| chr3:49606196
|
AC | A | 2 | a0002c0002t0001g0088a0002c0002t0001g0090 | 2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18778delC | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606196 | ||||||
| chr3:49606197
|
C | T | 41 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(38): Show | 41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18778C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606197 | ||||||
| chr3:49606199
|
T | A | 2 | a0002c0002t0001g0088a0002c0002t0001g0090 | 2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18776T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606199 | ||||||
| chr3:49606202
|
AT | A | 2 | a0002c0002t0001g0088a0002c0002t0001g0090 | 2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18771delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606202 | |||||
| chr3:49606203
|
T | A | 2 | a0010c0009t0001g0072a0014c0037t0025g0052 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.225-18772T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606203 | ||||||
| chr3:49606203
|
T | TTATATAT others(18): Show |
2 | a0001c0001t0002g0147a0001c0001t0030g0121 | 2 | HG02683.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.225-18766_225-1874 others(29): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606203 | |||||
| chr3:49606204
|
T | A | 39 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(36): Show | 39 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.225-18771T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606204 | ||||||
| chr3:49606209
|
AT | A | 2 | a0002c0002t0001g0088a0002c0002t0001g0090 | 2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18765delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606209 | ||||||
| chr3:49606211
|
G | A | 42 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(39): Show | 42 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.225-18764G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606211 | ||||||
| chr3:49606211
|
G | GTA | 3 | a0003c0004t0006g0029a0003c0004t0006g0032a0003c0004t0006g0033 | 3 | HG01516.hp1 HG01517.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.225-18758_225-1875 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606211 | |||||
| chr3:49606211
|
G | T | 1 | a0010c0009t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-18764G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606211 | ||||||
| chr3:49606212
|
T | A | 1 | a0010c0009t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-18763T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606212 | ||||||
| chr3:49606213
|
A | T | 39 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(36): Show | 39 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.225-18762A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606213 | ||||||
| chr3:49606214
|
T | A | 40 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(37): Show | 40 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.225-18761T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606214 | ||||||
| chr3:49606216
|
T | A | 39 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(36): Show | 39 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.225-18759T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606216 | ||||||
| chr3:49606218
|
T | A | 39 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(36): Show | 39 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.225-18757T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606218 | ||||||
| chr3:49606219
|
T | A | 3 | a0003c0003t0004g0046a0009c0014t0009g0042a0009c0014t0009g0099 | 3 | HG01081.hp2 HG01192.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.225-18756T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606219 | ||||||
| chr3:49606221
|
T | A | 3 | a0002c0002t0001g0088a0002c0002t0001g0090a0002c0020t0024g0166 | 3 | HG02723.hp2 NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18754T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606221 | ||||||
| chr3:49606223
|
T | A | 3 | a0002c0002t0001g0088a0002c0002t0001g0090a0002c0020t0024g0166 | 3 | HG02723.hp2 NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18752T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606223 | ||||||
| chr3:49606223
|
T | TATAAA | 22 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.225-18749_225-1874 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606223 | |||||
| chr3:49606224
|
A | AT | 32 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(29): Show | 32 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.225-18750dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606224 | |||||
| chr3:49606224
|
A | ATATTAAA others(76): Show |
1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225-18749_225-1874 others(87): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606224 | |||||
| chr3:49606225
|
T | TA | 7 | a0002c0002t0001g0152a0002c0002t0001g0180a0002c0002t0001g0181others(4): Show | 7 | HG01891.hp2 HG01934.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-18749dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606225 | |||||
| chr3:49606225
|
TAC | T | 2 | a0002c0002t0001g0088a0002c0002t0001g0090 | 2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18748_225-1874 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606225 | |||||
| chr3:49606227
|
C | T | 64 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.225-18748C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606227 | ||||||
| chr3:49606233
|
T | A | 23 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(20): Show | 23 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.225-18742T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606233 | ||||||
| chr3:49606235
|
ATATATG | A | 2 | a0002c0002t0001g0088a0002c0002t0001g0090 | 2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18734_225-1872 others(10): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606235 | |||||
| chr3:49606236
|
T | A | 41 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(38): Show | 41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18739T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606236 | ||||||
| chr3:49606238
|
T | A | 41 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(38): Show | 41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18737T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606238 | ||||||
| chr3:49606240
|
T | TTAAAA | 22 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.225-18735_225-1873 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606240 | ||||||
| chr3:49606240
|
TGTATATA others(5): Show |
T | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-18734_225-1872 others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606240 | ||||||
| chr3:49606241
|
G | A | 63 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.225-18734G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606241 | ||||||
| chr3:49606248
|
T | A | 41 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(38): Show | 41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18727T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606248 | ||||||
| chr3:49606248
|
T | TATTATAT others(302): Show |
1 | a0003c0004t0004g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.225-18727_225-1872 others(313): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606248 | ||||||
| chr3:49606248
|
T | TATTATAT others(302): Show |
1 | a0003c0004t0004g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.225-18727_225-1872 others(313): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606248 | ||||||
| chr3:49606248
|
T | TATTATAT others(272): Show |
1 | a0003c0004t0004g0038 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.225-18727_225-1872 others(283): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606248 | ||||||
| chr3:49606250
|
ATATAT | A | 2 | a0002c0002t0001g0088a0002c0002t0001g0090 | 2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18724_225-1872 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606250 | ||||||
| chr3:49606254
|
A | AT | 3 | a0003c0004t0004g0027a0003c0004t0004g0028a0003c0004t0004g0038 | 3 | HG01981.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.225-18720dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(247): Show |
1 | a0003c0003t0004g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(258): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(215): Show |
1 | a0003c0004t0004g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(226): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(217): Show |
2 | a0003c0003t0004g0020a0003c0003t0004g0023 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.225-18719_225-1871 others(228): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(242): Show |
1 | a0003c0003t0004g0014 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(253): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(249): Show |
3 | a0003c0003t0010g0010a0003c0003t0010g0011a0003c0003t0010g0012 | 3 | HG02622.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.225-18719_225-1871 others(260): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(333): Show |
1 | a0003c0004t0004g0026 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(344): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(303): Show |
1 | a0003c0033t0004g0025 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(314): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(88): Show |
1 | a0001c0001t0002g0113 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(99): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(87): Show |
1 | a0001c0001t0002g0115 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(98): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(247): Show |
2 | a0003c0003t0004g0018a0003c0003t0004g0019 | 2 | HG01074.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.225-18719_225-1871 others(258): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(307): Show |
1 | a0003c0003t0004g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(318): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(335): Show |
1 | a0003c0004t0023g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(346): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(331): Show |
3 | a0003c0004t0006g0029a0003c0004t0006g0032a0003c0004t0006g0033 | 3 | HG01516.hp1 HG01517.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.225-18719_225-1871 others(342): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606254
|
A | ATACATAT others(277): Show |
1 | a0003c0003t0004g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(288): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | |||||
| chr3:49606255
|
T | TACATATA others(260): Show |
1 | a0003c0004t0004g0024 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(271): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | |||||
| chr3:49606255
|
T | TACATATA others(269): Show |
1 | a0003c0003t0004g0022 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(280): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | |||||
| chr3:49606255
|
T | TACATATA others(268): Show |
1 | a0003c0003t0014g0160 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(279): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | |||||
| chr3:49606255
|
T | TACATATA others(231): Show |
1 | a0003c0023t0014g0157 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(242): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | |||||
| chr3:49606255
|
T | TACATATA others(323): Show |
1 | a0003c0004t0006g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(334): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | |||||
| chr3:49606255
|
T | TACATATA others(293): Show |
1 | a0003c0004t0006g0031 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(304): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | |||||
| chr3:49606255
|
T | TATTA | 22 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.225-18719_225-1871 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | |||||
| chr3:49606255
|
T | TTA | 41 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(38): Show | 41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18720_225-1871 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606255 | ||||||
| chr3:49606258
|
A | T | 2 | a0003c0004t0004g0024a0003c0023t0014g0157 | 2 | HG01070.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-18717A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606258 | ||||||
| chr3:49606267
|
A | ATATATTA others(53): Show |
1 | a0001c0001t0011g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18708_225-1870 others(64): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606267 | ||||||
| chr3:49606267
|
A | T | 45 | a0001c0001t0002g0113a0001c0001t0002g0115a0002c0002t0001g0063others(42): Show | 45 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.225-18708A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606267 | ||||||
| chr3:49606280
|
A | AT | 46 | a0001c0001t0002g0113a0001c0001t0002g0115a0001c0001t0011g0125others(43): Show | 46 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.225-18695_225-1869 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606280 | ||||||
| chr3:49606280
|
A | ATATATAT others(58): Show |
5 | a0001c0001t0002g0131a0001c0001t0002g0133a0001c0001t0002g0141others(2): Show | 5 | HG00642.hp2 HG01168.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-18695_225-1869 others(69): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606280 | ||||||
| chr3:49606289
|
T | A | 76 | a0001c0001t0002g0113a0001c0001t0002g0115a0001c0001t0002g0131others(73): Show | 76 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.225-18686T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606289 | ||||||
| chr3:49606289
|
T | TATATATA others(60): Show |
1 | a0022c0024t0007g0008 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.225-18672_225-1867 others(71): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606289 | |||||
| chr3:49606289
|
T | TATATATA others(60): Show |
6 | a0001c0001t0003g0047a0001c0001t0003g0048a0002c0002t0001g0059others(3): Show | 6 | HG00280.hp2 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-18643_225-1864 others(71): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606289 | |||||
| chr3:49606289
|
T | TATATATA others(59): Show |
65 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.225-18651_225-1865 others(70): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606289 | |||||
| chr3:49606289
|
T | TATATATA others(125): Show |
2 | a0003c0003t0004g0016a0003c0003t0004g0046 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.225-18665_225-1866 others(136): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606289 | |||||
| chr3:49606289
|
T | TATATATA others(16): Show |
22 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.225-18673_225-1867 others(27): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606289 | |||||
| chr3:49606311
|
A | AATATATA others(60): Show |
2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-18643_225-1864 others(71): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606311 | |||||
| chr3:49606322
|
A | AAATATAT others(57): Show |
1 | a0001c0001t0031g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-18651_225-1865 others(68): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606322 | |||||
| chr3:49606326
|
T | A | 2 | a0001c0001t0031g0142a0022c0024t0007g0008 | 2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.225-18649T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606326 | ||||||
| chr3:49606326
|
T | TATATATT others(60): Show |
9 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(6): Show | 9 | HG02257.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.225-18643_225-1864 others(71): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606326 | |||||
| chr3:49606415
|
T | G | 1 | a0002c0002t0001g0182 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-18560T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606415 | ||||||
| chr3:49606498
|
G | T | 2 | a0013c0012t0005g0084a0013c0012t0005g0085 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.225-18477G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606498 | ||||||
| chr3:49606550
|
A | G | 1 | a0003c0003t0004g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225-18425A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606550 | ||||||
| chr3:49606579
|
C | T | 59 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.225-18396C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606579 | ||||||
| chr3:49606592
|
C | T | 1 | a0002c0002t0001g0090 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.225-18383C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606592 | ||||||
| chr3:49606635
|
A | T | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.225-18340A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606635 | ||||||
| chr3:49606743
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0043others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-18232G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606743 | ||||||
| chr3:49606760
|
T | C | 61 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.225-18215T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606760 | ||||||
| chr3:49607254
|
G | A | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-17721G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49607254 | ||||||
| chr3:49607383
|
G | A | 2 | a0001c0001t0002g0097a0023c0028t0003g0150 | 2 | HG02738.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.225-17592G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49607383 | ||||||
| chr3:49607469
|
T | C | 1 | a0012c0011t0001g0067 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.225-17506T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49607469 | ||||||
| chr3:49607776
|
C | T | 155 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.225-17199C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49607776 | ||||||
| chr3:49607828
|
G | A | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225-17147G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49607828 | ||||||
| chr3:49608025
|
A | G | 158 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.225-16950A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608025 | ||||||
| chr3:49608069
|
C | T | 6 | a0001c0001t0003g0041a0001c0001t0003g0122a0001c0001t0003g0128others(3): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-16906C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608069 | ||||||
| chr3:49608278
|
A | T | 2 | a0003c0003t0014g0160a0003c0023t0014g0157 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-16697A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608278 | ||||||
| chr3:49608359
|
C | T | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-16616C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608359 | ||||||
| chr3:49608387
|
G | T | 1 | a0001c0001t0003g0048 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.225-16588G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608387 | ||||||
| chr3:49608567
|
C | T | 5 | a0002c0002t0005g0062a0002c0002t0005g0074a0002c0002t0005g0075others(2): Show | 5 | HG01081.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-16408C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608567 | ||||||
| chr3:49608717
|
A | G | 2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-16258A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608717 | ||||||
| chr3:49608766
|
T | C | 1 | a0001c0017t0002g0106 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.225-16209T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608766 | ||||||
| chr3:49608773
|
A | T | 4 | a0001c0001t0011g0098a0001c0001t0011g0125a0001c0001t0011g0127others(1): Show | 4 | HG00323.hp2 HG01106.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-16202A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608773 | ||||||
| chr3:49608829
|
G | GA | 4 | a0001c0001t0021g0145a0006c0005t0008g0162a0010c0009t0001g0072others(1): Show | 4 | HG04115.hp2 NA18951.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-16146_225-1614 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608829 | ||||||
| chr3:49608830
|
G | A | 173 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.225-16145G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608830 | ||||||
| chr3:49608883
|
G | C | 1 | a0019c0026t0002g0100 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.225-16092G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608883 | ||||||
| chr3:49609089
|
C | CT | 14 | a0001c0001t0012g0057a0002c0002t0001g0078a0002c0002t0001g0079others(11): Show | 14 | HG00099.hp1 HG00544.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.225-15863dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49609089 | |||||
| chr3:49609089
|
CT | C | 73 | a0001c0001t0002g0095a0001c0001t0002g0102a0001c0001t0002g0104others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.225-15863delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49609089 | |||||
| chr3:49609236
|
G | A | 156 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.225-15739G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49609236 | ||||||
| chr3:49609268
|
A | AT | 6 | a0001c0001t0002g0178a0002c0002t0001g0053a0002c0002t0016g0040others(3): Show | 6 | HG01433.hp1 HG02738.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-15692dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49609268 | |||||
| chr3:49609340
|
C | T | 1 | a0002c0002t0001g0076 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.225-15635C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49609340 | ||||||
| chr3:49609548
|
T | C | 158 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.225-15427T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49609548 | ||||||
| chr3:49609971
|
T | A | 156 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.225-15004T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49609971 | ||||||
| chr3:49610354
|
G | A | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225-14621G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49610354 | ||||||
| chr3:49610388
|
G | T | 83 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.225-14587G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49610388 | ||||||
| chr3:49610451
|
G | A | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-14524G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49610451 | ||||||
| chr3:49610557
|
C | T | 1 | a0002c0002t0001g0061 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.225-14418C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49610557 | ||||||
| chr3:49610559
|
G | A | 1 | a0002c0002t0001g0055 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.225-14416G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49610559 | ||||||
| chr3:49610584
|
C | CA | 44 | a0001c0001t0007g0007a0001c0001t0012g0057a0002c0002t0001g0053others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.225-14369dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49610584 | |||||
| chr3:49610584
|
C | CAA | 23 | a0001c0001t0007g0006a0001c0001t0007g0043a0001c0001t0011g0127others(20): Show | 23 | HG00323.hp2 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.225-14370_225-1436 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49610584 | |||||
| chr3:49610584
|
C | CAAA | 68 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0104others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.225-14371_225-1436 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49610584 | |||||
| chr3:49610584
|
C | CAAAA | 14 | a0001c0001t0002g0102a0001c0001t0002g0135a0001c0001t0002g0151others(11): Show | 14 | HG01106.hp2 HG01109.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.225-14372_225-1436 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49610584 | |||||
| chr3:49611054
|
A | G | 1 | a0003c0003t0004g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.225-13921A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49611054 | ||||||
| chr3:49611279
|
A | C | 1 | a0001c0001t0002g0178 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.225-13696A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49611279 | ||||||
| chr3:49611334
|
C | T | 4 | a0005c0007t0007g0002a0005c0007t0034g0004a0005c0032t0007g0080others(1): Show | 4 | HG02451.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-13641C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49611334 | ||||||
| chr3:49611475
|
G | C | 1 | a0002c0002t0001g0088 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.225-13500G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49611475 | ||||||
| chr3:49611638
|
C | T | 82 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.225-13337C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49611638 | ||||||
| chr3:49612001
|
C | A | 13 | a0003c0003t0004g0014a0003c0003t0004g0016a0003c0003t0004g0017others(10): Show | 13 | HG01074.hp2 HG01884.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.225-12974C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612001 | ||||||
| chr3:49612139
|
A | AT | 68 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.225-12822dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49612139 | |||||
| chr3:49612139
|
A | ATT | 79 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(76): Show | 79 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.225-12823_225-1282 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49612139 | |||||
| chr3:49612139
|
A | ATTT | 7 | a0001c0001t0002g0112a0001c0001t0002g0151a0001c0001t0002g0177others(4): Show | 7 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.225-12824_225-1282 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49612139 | |||||
| chr3:49612159
|
A | G | 1 | a0001c0001t0003g0138 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.225-12816A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612159 | ||||||
| chr3:49612293
|
G | C | 2 | a0003c0003t0014g0160a0003c0023t0014g0157 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-12682G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612293 | ||||||
| chr3:49612388
|
G | A | 1 | a0001c0001t0003g0132 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.225-12587G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612388 | ||||||
| chr3:49612440
|
A | G | 6 | a0003c0004t0006g0029a0003c0004t0006g0030a0003c0004t0006g0031others(3): Show | 6 | HG01516.hp1 HG01517.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-12535A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612440 | ||||||
| chr3:49612454
|
C | T | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG01257.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.225-12521C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612454 | ||||||
| chr3:49612556
|
C | G | 61 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.225-12419C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612556 | ||||||
| chr3:49612962
|
G | A | 61 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.225-12013G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612962 | ||||||
| chr3:49613275
|
T | TTA | 91 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.225-11685_225-1168 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613275 | |||||
| chr3:49613292
|
C | T | 1 | a0001c0001t0011g0127 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.225-11683C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613292 | ||||||
| chr3:49613300
|
G | C | 1 | a0001c0001t0011g0127 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.225-11675G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613300 | ||||||
| chr3:49613303
|
C | A | 1 | a0001c0001t0011g0127 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.225-11672C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613303 | ||||||
| chr3:49613303
|
C | CAAGAGAG others(15): Show |
1 | a0004c0006t0002g0036 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.225-11672_225-1167 others(26): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613303 | ||||||
| chr3:49613303
|
C | CAAGAGAG others(19): Show |
1 | a0004c0022t0002g0034 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.225-11672_225-1167 others(30): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613303 | ||||||
| chr3:49613303
|
C | CGA | 7 | a0001c0001t0029g0158a0002c0002t0001g0077a0002c0002t0001g0078others(4): Show | 7 | HG02055.hp2 HG02698.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-11627_225-1162 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGA | 5 | a0002c0002t0001g0053a0003c0004t0004g0028a0003c0004t0023g0045others(2): Show | 5 | HG01069.hp2 HG02738.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-11629_225-1162 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGAGA | 12 | a0001c0001t0002g0097a0001c0001t0002g0124a0001c0001t0011g0125others(9): Show | 12 | HG00280.hp2 HG00642.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.225-11631_225-1162 others(10): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGAGAG others(1): Show |
14 | a0001c0001t0002g0147a0001c0001t0003g0123a0001c0001t0007g0006others(11): Show | 14 | HG00323.hp1 HG01070.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.225-11633_225-1162 others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGAGAG others(3): Show |
17 | a0001c0001t0002g0151a0001c0001t0002g0178a0001c0001t0003g0120others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.225-11635_225-1162 others(14): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGAGAG others(5): Show |
17 | a0001c0001t0002g0131a0001c0001t0003g0041a0001c0001t0003g0119others(14): Show | 17 | HG00544.hp2 HG01257.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.225-11637_225-1162 others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGAGAG others(7): Show |
22 | a0001c0001t0002g0113a0001c0001t0002g0139a0001c0001t0002g0140others(19): Show | 22 | HG00099.hp2 HG00733.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.225-11639_225-1162 others(18): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGAGAG others(9): Show |
18 | a0001c0001t0002g0095a0001c0001t0002g0115a0001c0001t0002g0141others(15): Show | 18 | HG01167.hp2 HG01168.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.225-11641_225-1162 others(20): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGAGAG others(11): Show |
11 | a0001c0001t0002g0112a0001c0001t0003g0122a0001c0001t0018g0109others(8): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.225-11643_225-1162 others(22): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGAGAG others(13): Show |
10 | a0001c0001t0002g0105a0001c0001t0002g0133a0001c0001t0002g0177others(7): Show | 10 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.225-11645_225-1162 others(24): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGAGAG others(15): Show |
12 | a0001c0001t0002g0107a0001c0001t0009g0094a0001c0001t0009g0149others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.225-11647_225-1162 others(26): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGAGAG others(17): Show |
5 | a0001c0001t0002g0148a0001c0001t0003g0096a0002c0002t0001g0087others(2): Show | 5 | HG00099.hp1 HG00140.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-11649_225-1162 others(28): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGAGAG others(19): Show |
4 | a0001c0001t0002g0104a0001c0001t0002g0110a0001c0001t0012g0116others(1): Show | 4 | HG01515.hp2 HG02698.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-11651_225-1162 others(30): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGAGAG others(21): Show |
1 | a0004c0006t0002g0035 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.225-11653_225-1162 others(32): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGAGAG others(23): Show |
1 | a0001c0001t0003g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.225-11655_225-1162 others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGCGAG others(19): Show |
2 | a0001c0001t0002g0102a0001c0001t0002g0135 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.225-11669_225-1166 others(30): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
C | CGAGCGAG others(21): Show |
1 | a0001c0001t0002g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.225-11669_225-1166 others(32): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
CGA | C | 5 | a0002c0002t0005g0062a0002c0002t0005g0074a0002c0002t0005g0075others(2): Show | 5 | HG01081.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-11627_225-1162 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613303
|
CGAGAGAG others(1): Show |
C | 2 | a0002c0020t0024g0166a0014c0037t0025g0052 | 2 | HG01884.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.225-11633_225-1162 others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | |||||
| chr3:49613305
|
A | C | 1 | a0001c0001t0011g0127 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.225-11670A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613305 | ||||||
| chr3:49613307
|
A | AGAGAGAG others(6): Show |
1 | a0001c0001t0032g0144 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.225-11667_225-1165 others(17): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613307 | |||||
| chr3:49613349
|
A | AGAGAGAG others(4): Show |
1 | a0001c0001t0003g0156 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.225-11626_225-1162 others(15): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613349 | ||||||
| chr3:49613349
|
A | AGAGAGAG others(16): Show |
1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.225-11626_225-1162 others(27): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613349 | ||||||
| chr3:49613351
|
G | A | 1 | a0015c0035t0002g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.225-11624G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613351 | ||||||
| chr3:49613499
|
A | T | 4 | a0001c0001t0002g0124a0001c0001t0002g0148a0011c0010t0001g0165others(1): Show | 4 | HG02970.hp1 HG03710.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-11476A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613499 | ||||||
| chr3:49613502
|
A | T | 145 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.225-11473A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613502 | ||||||
| chr3:49613505
|
T | A | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-11470T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613505 | ||||||
| chr3:49613666
|
C | CT | 89 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.225-11296dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613666 | |||||
| chr3:49613777
|
G | A | 61 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.225-11198G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613777 | ||||||
| chr3:49614024
|
G | A | 1 | a0001c0001t0002g0178 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.225-10951G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614024 | ||||||
| chr3:49614051
|
C | CT | 68 | a0001c0001t0002g0097a0001c0001t0002g0114a0001c0001t0002g0131others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.225-10900dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49614051 | |||||
| chr3:49614051
|
C | CTT | 9 | a0001c0001t0009g0149a0002c0002t0001g0053a0002c0002t0001g0055others(6): Show | 9 | HG00639.hp1 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.225-10901_225-1090 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49614051 | |||||
| chr3:49614051
|
C | CTTT | 5 | a0002c0002t0001g0170a0002c0002t0001g0174a0002c0002t0001g0175others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-10902_225-1090 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49614051 | |||||
| chr3:49614051
|
C | CTTTT | 6 | a0002c0002t0001g0088a0002c0002t0001g0089a0002c0002t0001g0090others(3): Show | 6 | HG00733.hp1 HG00735.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-10903_225-1090 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49614051 | |||||
| chr3:49614101
|
C | T | 12 | a0002c0002t0001g0088a0002c0002t0001g0089a0002c0002t0001g0090others(9): Show | 12 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.225-10874C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614101 | ||||||
| chr3:49614113
|
G | T | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-10862G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614113 | ||||||
| chr3:49614128
|
C | T | 2 | a0003c0003t0014g0160a0003c0023t0014g0157 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-10847C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614128 | ||||||
| chr3:49614170
|
C | T | 7 | a0001c0001t0002g0104a0004c0006t0002g0035a0004c0006t0002g0036others(4): Show | 7 | HG00140.hp1 HG00733.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-10805C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614170 | ||||||
| chr3:49614208
|
C | T | 1 | a0004c0022t0002g0034 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.225-10767C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614208 | ||||||
| chr3:49614522
|
C | T | 1 | a0003c0004t0004g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.225-10453C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614522 | ||||||
| chr3:49614537
|
C | G | 9 | a0002c0002t0001g0167a0002c0002t0001g0168a0002c0002t0001g0170others(6): Show | 9 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.225-10438C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614537 | ||||||
| chr3:49614715
|
T | C | 155 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.225-10260T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614715 | ||||||
| chr3:49614723
|
C | T | 88 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.225-10252C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614723 | ||||||
| chr3:49614840
|
A | G | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0024c0029t0003g0049 | 3 | HG02258.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.225-10135A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614840 | ||||||
| chr3:49614902
|
G | T | 1 | a0002c0002t0001g0086 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.225-10073G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614902 | ||||||
| chr3:49615164
|
C | G | 5 | a0004c0006t0002g0035a0004c0006t0002g0036a0004c0006t0002g0037others(2): Show | 5 | HG00140.hp1 HG00733.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-9811C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49615164 | ||||||
| chr3:49615945
|
A | G | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.225-9030A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49615945 | ||||||
| chr3:49616024
|
C | T | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.225-8951C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49616024 | ||||||
| chr3:49616508
|
C | A | 2 | a0008c0015t0002g0103a0008c0015t0002g0108 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.225-8467C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49616508 | ||||||
| chr3:49617184
|
G | A | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-7791G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49617184 | ||||||
| chr3:49617210
|
A | G | 1 | a0001c0001t0030g0121 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.225-7765A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49617210 | ||||||
| chr3:49617277
|
AATACATT others(10): Show |
A | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-7694_225-7678d others(19): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617277 | |||||
| chr3:49617277
|
AATACATT others(14): Show |
A | 55 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(52): Show | 55 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.225-7694_225-7674d others(23): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617277 | |||||
| chr3:49617277
|
AATACATT others(16): Show |
A | 4 | a0002c0002t0001g0081a0002c0002t0001g0082a0002c0002t0001g0083others(1): Show | 4 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-7694_225-7672d others(25): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617277 | |||||
| chr3:49617283
|
T | TTA | 3 | a0003c0004t0004g0038a0003c0004t0023g0045a0003c0033t0004g0025 | 3 | HG01069.hp2 HG01981.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.225-7657_225-7656d others(4): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | |||||
| chr3:49617283
|
T | TTATA | 2 | a0003c0003t0004g0013a0003c0003t0004g0046 | 2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.225-7659_225-7656d others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | |||||
| chr3:49617283
|
T | TTATATAT others(3): Show |
2 | a0003c0004t0004g0028a0003c0004t0006g0032 | 2 | HG01517.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.225-7665_225-7656d others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | |||||
| chr3:49617283
|
T | TTATATAT others(5): Show |
3 | a0003c0004t0004g0024a0003c0004t0006g0029a0003c0004t0006g0033 | 3 | HG01070.hp1 HG01516.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.225-7667_225-7656d others(14): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | |||||
| chr3:49617283
|
T | TTATATAT others(7): Show |
3 | a0003c0004t0006g0030a0003c0004t0006g0117a0003c0023t0014g0157 | 3 | HG02615.hp2 HG03453.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.225-7669_225-7656d others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | |||||
| chr3:49617283
|
T | TTATATAT others(25): Show |
1 | a0003c0004t0006g0031 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.225-7687_225-7656d others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | |||||
| chr3:49617283
|
TTA | T | 4 | a0003c0003t0004g0022a0005c0007t0007g0002a0005c0032t0007g0080others(1): Show | 4 | HG01884.hp1 HG02683.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-7657_225-7656d others(4): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | |||||
| chr3:49617283
|
TTATA | T | 9 | a0003c0003t0004g0014a0003c0003t0004g0016a0003c0003t0004g0017others(6): Show | 9 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.225-7659_225-7656d others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | |||||
| chr3:49617283
|
TTATATA | T | 4 | a0003c0003t0004g0021a0003c0003t0010g0010a0003c0003t0010g0011others(1): Show | 4 | HG02622.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-7661_225-7656d others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | |||||
| chr3:49617283
|
TTATATAT others(5): Show |
T | 1 | a0003c0003t0004g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.225-7667_225-7656d others(14): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | |||||
| chr3:49617283
|
TTATATAT others(7): Show |
T | 4 | a0001c0001t0002g0131a0007c0013t0013g0050a0007c0013t0013g0051others(1): Show | 4 | HG02572.hp2 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-7669_225-7656d others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | |||||
| chr3:49617283
|
TTATATAT others(9): Show |
T | 84 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.225-7671_225-7656d others(18): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | |||||
| chr3:49617430
|
C | A | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG01257.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.225-7545C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49617430 | ||||||
| chr3:49618278
|
C | T | 2 | a0002c0002t0005g0039a0002c0002t0016g0040 | 2 | NA19003.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.225-6697C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49618278 | ||||||
| chr3:49618494
|
T | A | 12 | a0003c0004t0004g0024a0003c0004t0004g0026a0003c0004t0004g0027others(9): Show | 12 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.225-6481T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49618494 | ||||||
| chr3:49618570
|
A | G | 7 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0071others(4): Show | 7 | HG01167.hp1 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-6405A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49618570 | ||||||
| chr3:49618610
|
A | G | 2 | a0001c0001t0002g0107a0015c0035t0002g0134 | 2 | NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.225-6365A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49618610 | ||||||
| chr3:49619094
|
T | A | 1 | a0002c0002t0017g0058 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.225-5881T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49619094 | ||||||
| chr3:49619097
|
CTGAA | C | 171 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.225-5864_225-5861d others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49619097 | |||||
| chr3:49619132
|
G | A | 1 | a0021c0025t0028g0101 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.225-5843G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49619132 | ||||||
| chr3:49619356
|
G | T | 82 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.225-5619G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49619356 | ||||||
| chr3:49619729
|
C | A | 1 | a0018c0031t0002g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.225-5246C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49619729 | ||||||
| chr3:49619776
|
G | C | 2 | a0001c0001t0003g0126a0001c0001t0003g0132 | 2 | HG00639.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.225-5199G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49619776 | ||||||
| chr3:49619983
|
CT | C | 155 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.225-4991delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49619983 | ||||||
| chr3:49620008
|
A | G | 155 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.225-4967A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620008 | ||||||
| chr3:49620038
|
A | T | 1 | a0001c0001t0003g0122 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.225-4937A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620038 | ||||||
| chr3:49620192
|
C | T | 1 | a0003c0003t0004g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225-4783C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620192 | ||||||
| chr3:49620288
|
G | A | 1 | a0018c0031t0002g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.225-4687G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620288 | ||||||
| chr3:49620419
|
C | T | 73 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.225-4556C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620419 | ||||||
| chr3:49620651
|
A | G | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.225-4324A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620651 | ||||||
| chr3:49620722
|
C | T | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0043others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-4253C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620722 | ||||||
| chr3:49620805
|
C | T | 1 | a0002c0002t0001g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.225-4170C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620805 | ||||||
| chr3:49620943
|
A | G | 1 | a0001c0001t0002g0177 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.225-4032A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620943 | ||||||
| chr3:49621104
|
A | C | 1 | a0003c0003t0004g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225-3871A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49621104 | ||||||
| chr3:49621745
|
T | C | 2 | a0002c0002t0001g0088a0002c0002t0001g0090 | 2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-3230T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49621745 | ||||||
| chr3:49622324
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.225-2651G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49622324 | ||||||
| chr3:49622375
|
A | G | 1 | a0003c0003t0004g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225-2600A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49622375 | ||||||
| chr3:49622562
|
C | G | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225-2413C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49622562 | ||||||
| chr3:49622584
|
C | T | 1 | a0002c0002t0016g0040 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.225-2391C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49622584 | ||||||
| chr3:49623079
|
T | A | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-1896T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49623079 | ||||||
| chr3:49623209
|
G | A | 2 | a0002c0008t0001g0169a0002c0008t0001g0173 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.225-1766G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49623209 | ||||||
| chr3:49623636
|
C | T | 2 | a0003c0003t0014g0160a0003c0023t0014g0157 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-1339C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49623636 | ||||||
| chr3:49624028
|
T | G | 1 | a0003c0003t0004g0014 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.225-947T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49624028 | ||||||
| chr3:49624201
|
C | T | 10 | a0003c0004t0004g0024a0003c0004t0004g0026a0003c0004t0004g0038others(7): Show | 10 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.225-774C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49624201 | ||||||
| chr3:49624299
|
C | CATTTTTT others(6): Show |
1 | a0001c0001t0002g0110 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.225-676_225-675ins others(13): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49624299 | ||||||
| chr3:49624300
|
C | CTTTTTTT others(4): Show |
1 | a0007c0013t0013g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.225-668_225-658dup others(11): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49624300 | |||||
| chr3:49624300
|
C | CTTTTTTT others(5): Show |
23 | a0001c0001t0012g0057a0002c0002t0001g0055a0002c0002t0001g0061others(20): Show | 23 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.225-669_225-658dup others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49624300 | |||||
| chr3:49624300
|
C | CTTTTTTT others(6): Show |
72 | a0001c0001t0002g0102a0001c0001t0002g0104a0001c0001t0002g0107others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.225-670_225-658dup others(13): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49624300 | |||||
| chr3:49624300
|
C | CTTTTTTT others(7): Show |
45 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0105others(42): Show | 45 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.225-671_225-658dup others(14): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49624300 | |||||
| chr3:49624300
|
C | CTTTTTTT others(8): Show |
9 | a0001c0001t0002g0115a0001c0001t0002g0148a0001c0001t0003g0096others(6): Show | 9 | HG00735.hp1 HG01109.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.225-672_225-658dup others(15): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49624300 | |||||
| chr3:49624300
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0029g0158 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.225-673_225-658dup others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49624300 | |||||
| chr3:49624300
|
C | T | 1 | a0001c0001t0002g0110 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.225-675C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49624300 | ||||||
| chr3:49625856
|
G | A | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.633+473G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49625856 | ||||||
| chr3:49626261
|
G | A | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0043 | 3 | HG02257.hp2 HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.633+878G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49626261 | ||||||
| chr3:49626357
|
G | C | 1 | a0001c0001t0002g0095 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.633+974G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49626357 | ||||||
| chr3:49626456
|
T | C | 2 | a0001c0001t0002g0131a0001c0001t0002g0139 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.633+1073T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49626456 | ||||||
| chr3:49626555
|
T | G | 1 | a0001c0001t0002g0104 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.633+1172T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49626555 | ||||||
| chr3:49627013
|
T | G | 1 | a0002c0002t0005g0062 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.633+1630T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627013 | ||||||
| chr3:49627020
|
T | C | 1 | a0001c0001t0019g0093 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.633+1637T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627020 | ||||||
| chr3:49627047
|
G | A | 1 | a0002c0002t0001g0152 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.633+1664G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627047 | ||||||
| chr3:49627334
|
A | G | 60 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.633+1951A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627334 | ||||||
| chr3:49627409
|
T | A | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0024c0029t0003g0049 | 3 | HG02258.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.633+2026T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627409 | ||||||
| chr3:49627843
|
T | C | 2 | a0003c0003t0014g0160a0003c0023t0014g0157 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.633+2460T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627843 | ||||||
| chr3:49627957
|
G | A | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.633+2574G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627957 | ||||||
| chr3:49628179
|
A | G | 1 | a0001c0001t0003g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.633+2796A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49628179 | ||||||
| chr3:49628541
|
G | T | 2 | a0001c0001t0002g0147a0001c0001t0021g0145 | 2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.633+3158G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49628541 | ||||||
| chr3:49628543
|
T | G | 60 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.633+3160T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49628543 | ||||||
| chr3:49629109
|
G | A | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.633+3726G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49629109 | ||||||
| chr3:49629531
|
C | A | 59 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.633+4148C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49629531 | ||||||
| chr3:49629741
|
C | A | 1 | a0001c0001t0002g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.633+4358C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49629741 | ||||||
| chr3:49629753
|
C | T | 3 | a0003c0003t0010g0010a0003c0003t0010g0011a0003c0003t0010g0012 | 3 | HG02622.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.633+4370C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49629753 | ||||||
| chr3:49629909
|
G | A | 1 | a0001c0001t0002g0105 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.633+4526G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49629909 | ||||||
| chr3:49629980
|
A | T | 1 | a0001c0001t0002g0112 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.633+4597A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49629980 | ||||||
| chr3:49630258
|
T | C | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.633+4875T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49630258 | ||||||
| chr3:49630443
|
A | G | 1 | a0001c0001t0002g0151 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.633+5060A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49630443 | ||||||
| chr3:49631170
|
C | T | 1 | a0011c0010t0001g0165 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.633+5787C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631170 | ||||||
| chr3:49631316
|
G | A | 2 | a0001c0001t0002g0131a0001c0001t0002g0139 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.633+5933G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631316 | ||||||
| chr3:49631346
|
A | G | 1 | a0001c0001t0003g0130 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.633+5963A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631346 | ||||||
| chr3:49631377
|
G | A | 1 | a0001c0001t0002g0095 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.633+5994G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631377 | ||||||
| chr3:49631500
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.633+6117A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631500 | ||||||
| chr3:49631541
|
G | GAGTA | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0024c0029t0003g0049 | 3 | HG02258.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.633+6161_633+6164d others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49631541 | |||||
| chr3:49631557
|
C | CA | 13 | a0001c0001t0002g0104a0001c0001t0003g0047a0001c0001t0003g0048others(10): Show | 13 | HG01074.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.633+6192dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49631557 | |||||
| chr3:49631557
|
CA | C | 10 | a0002c0002t0001g0077a0002c0002t0001g0152a0002c0002t0001g0180others(7): Show | 10 | HG01081.hp2 HG01257.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.633+6192delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49631557 | |||||
| chr3:49631633
|
T | C | 2 | a0001c0001t0002g0147a0001c0001t0021g0145 | 2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.633+6250T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631633 | ||||||
| chr3:49631657
|
G | T | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.633+6274G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631657 | ||||||
| chr3:49632515
|
G | A | 12 | a0001c0001t0002g0095a0001c0001t0002g0148a0001c0001t0003g0118others(9): Show | 12 | HG00639.hp2 HG01167.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.633+7132G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49632515 | ||||||
| chr3:49632696
|
C | T | 4 | a0001c0001t0009g0094a0001c0001t0009g0149a0009c0014t0009g0042others(1): Show | 4 | HG01081.hp2 HG01192.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.633+7313C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49632696 | ||||||
| chr3:49633217
|
G | A | 82 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.633+7834G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49633217 | ||||||
| chr3:49633301
|
C | CA | 8 | a0001c0001t0002g0151a0002c0002t0001g0152a0002c0002t0001g0180others(5): Show | 8 | HG01891.hp2 HG01934.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.633+7932dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49633301 | |||||
| chr3:49633604
|
G | A | 13 | a0001c0001t0012g0057a0002c0002t0001g0054a0002c0002t0001g0055others(10): Show | 13 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.633+8221G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49633604 | ||||||
| chr3:49633753
|
C | T | 94 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.633+8370C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49633753 | ||||||
| chr3:49633791
|
T | C | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.633+8408T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49633791 | ||||||
| chr3:49634002
|
C | T | 1 | a0022c0024t0007g0008 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.634-8266C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49634002 | ||||||
| chr3:49634221
|
A | C | 82 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.634-8047A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49634221 | ||||||
| chr3:49634413
|
T | A | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.634-7855T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49634413 | ||||||
| chr3:49635633
|
T | C | 3 | a0003c0003t0010g0010a0003c0003t0010g0011a0003c0003t0010g0012 | 3 | HG02622.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.634-6635T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49635633 | ||||||
| chr3:49635833
|
C | T | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.634-6435C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49635833 | ||||||
| chr3:49635852
|
G | C | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.634-6416G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49635852 | ||||||
| chr3:49635937
|
G | C | 1 | a0001c0001t0002g0113 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.634-6331G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49635937 | ||||||
| chr3:49636229
|
A | G | 10 | a0003c0004t0004g0024a0003c0004t0004g0026a0003c0004t0004g0038others(7): Show | 10 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.634-6039A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49636229 | ||||||
| chr3:49636422
|
G | C | 1 | a0001c0001t0011g0127 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.634-5846G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49636422 | ||||||
| chr3:49636714
|
C | G | 61 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.634-5554C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49636714 | ||||||
| chr3:49636817
|
A | G | 2 | a0001c0001t0003g0159a0001c0001t0029g0158 | 2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.634-5451A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49636817 | ||||||
| chr3:49636910
|
C | T | 171 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.634-5358C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49636910 | ||||||
| chr3:49637002
|
A | G | 1 | a0001c0001t0002g0113 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.634-5266A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49637002 | ||||||
| chr3:49637025
|
A | G | 61 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.634-5243A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49637025 | ||||||
| chr3:49637425
|
G | A | 1 | a0022c0024t0007g0008 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.634-4843G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49637425 | ||||||
| chr3:49637642
|
G | A | 3 | a0001c0001t0002g0097a0001c0001t0002g0124a0023c0028t0003g0150 | 3 | HG02738.hp2 HG03710.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.634-4626G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49637642 | ||||||
| chr3:49637709
|
T | A | 88 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.634-4559T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49637709 | ||||||
| chr3:49637901
|
C | G | 60 | a0001c0001t0012g0057a0002c0002t0001g0053a0002c0002t0001g0054others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.634-4367C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49637901 | ||||||
| chr3:49638038
|
A | G | 1 | a0024c0029t0003g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.634-4230A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638038 | ||||||
| chr3:49638075
|
G | A | 1 | a0003c0003t0004g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.634-4193G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638075 | ||||||
| chr3:49638124
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.634-4144G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638124 | ||||||
| chr3:49638189
|
C | G | 1 | a0001c0001t0002g0133 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.634-4079C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638189 | ||||||
| chr3:49638296
|
A | G | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.634-3972A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638296 | ||||||
| chr3:49638404
|
G | A | 1 | a0001c0001t0020g0092 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.634-3864G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638404 | ||||||
| chr3:49638442
|
G | C | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.634-3826G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638442 | ||||||
| chr3:49638531
|
ATGCTGGG others(8): Show |
A | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.634-3734_634-3720d others(17): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49638531 | |||||
| chr3:49638665
|
G | A | 1 | a0007c0013t0013g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.634-3603G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638665 | ||||||
| chr3:49639199
|
C | CT | 61 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0043others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.634-3052dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49639199 | |||||
| chr3:49639464
|
C | T | 1 | a0020c0030t0002g0143 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.634-2804C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49639464 | ||||||
| chr3:49639487
|
G | C | 1 | a0001c0001t0012g0057 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.634-2781G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49639487 | ||||||
| chr3:49639633
|
G | T | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0043others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.634-2635G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49639633 | ||||||
| chr3:49639646
|
A | G | 3 | a0003c0004t0004g0015a0003c0004t0004g0027a0003c0004t0004g0028 | 3 | HG03098.hp1 HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.634-2622A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49639646 | ||||||
| chr3:49639675
|
GAGGC | G | 2 | a0003c0003t0014g0160a0003c0023t0014g0157 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.634-2589_634-2586d others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49639675 | |||||
| chr3:49639859
|
C | G | 95 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.634-2409C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49639859 | ||||||
| chr3:49640044
|
C | CAT | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.634-2224_634-2223i others(4): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49640044 | ||||||
| chr3:49640062
|
G | A | 1 | a0003c0003t0004g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.634-2206G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49640062 | ||||||
| chr3:49640164
|
A | G | 1 | a0001c0027t0003g0186 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.634-2104A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49640164 | ||||||
| chr3:49640644
|
G | A | 83 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.634-1624G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49640644 | ||||||
| chr3:49640780
|
G | A | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.634-1488G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49640780 | ||||||
| chr3:49640874
|
A | T | 58 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0055others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.634-1394A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49640874 | ||||||
| chr3:49641218
|
A | G | 60 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0055others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.634-1050A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49641218 | ||||||
| chr3:49641280
|
A | G | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.634-988A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49641280 | ||||||
| chr3:49641639
|
G | A | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.634-629G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49641639 | ||||||
| chr3:49641979
|
G | A | 2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.634-289G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49641979 | ||||||
| chr3:49643540
|
G | A | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1518+388G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49643540 | ||||||
| chr3:49643875
|
C | T | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0043others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1518+723C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49643875 | ||||||
| chr3:49643910
|
G | A | 1 | a0001c0001t0032g0144 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1518+758G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49643910 | ||||||
| chr3:49644187
|
G | T | 6 | a0001c0001t0003g0041a0001c0001t0003g0122a0001c0001t0003g0128others(3): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1518+1035G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49644187 | ||||||
| chr3:49644271
|
A | G | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1518+1119A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49644271 | ||||||
| chr3:49644294
|
C | T | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1518+1142C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49644294 | ||||||
| chr3:49644545
|
C | T | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0043 | 3 | HG02257.hp2 HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1518+1393C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49644545 | ||||||
| chr3:49644781
|
C | G | 1 | a0003c0003t0004g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1518+1629C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49644781 | ||||||
| chr3:49644878
|
G | A | 60 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0055others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1518+1726G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49644878 | ||||||
| chr3:49645531
|
T | A | 2 | a0003c0003t0014g0160a0003c0023t0014g0157 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1518+2379T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49645531 | ||||||
| chr3:49645540
|
C | T | 1 | a0018c0031t0002g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1518+2388C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49645540 | ||||||
| chr3:49646093
|
G | A | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1518+2941G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49646093 | ||||||
| chr3:49646175
|
T | A | 12 | a0003c0003t0004g0014a0003c0003t0004g0016a0003c0003t0004g0017others(9): Show | 12 | HG01074.hp2 HG01884.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1518+3023T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49646175 | ||||||
| chr3:49646542
|
T | C | 1 | a0002c0002t0005g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1518+3390T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49646542 | ||||||
| chr3:49646786
|
T | A | 4 | a0001c0001t0003g0159a0001c0001t0029g0158a0003c0003t0014g0160others(1): Show | 4 | HG03041.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1518+3634T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49646786 | ||||||
| chr3:49647314
|
T | C | 1 | a0003c0003t0014g0160 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1519-3298T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49647314 | ||||||
| chr3:49647484
|
C | G | 60 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0055others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1519-3128C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49647484 | ||||||
| chr3:49647640
|
G | A | 74 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.1519-2972G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49647640 | ||||||
| chr3:49648073
|
A | G | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1519-2539A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49648073 | ||||||
| chr3:49648159
|
A | G | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1519-2453A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49648159 | ||||||
| chr3:49648188
|
A | G | 1 | a0001c0001t0011g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1519-2424A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49648188 | ||||||
| chr3:49648783
|
CA | C | 3 | a0003c0003t0004g0017a0003c0003t0004g0019a0003c0003t0004g0023 | 3 | HG01074.hp2 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1519-1828delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49648783 | ||||||
| chr3:49648880
|
A | T | 2 | a0001c0001t0012g0116a0001c0001t0012g0136 | 2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1519-1732A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49648880 | ||||||
| chr3:49649215
|
T | G | 1 | a0001c0001t0011g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1519-1397T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49649215 | ||||||
| chr3:49649249
|
T | C | 60 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0055others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1519-1363T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49649249 | ||||||
| chr3:49649610
|
T | C | 157 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1519-1002T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49649610 | ||||||
| chr3:49649615
|
G | C | 2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1519-997G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49649615 | ||||||
| chr3:49649681
|
T | C | 1 | a0002c0020t0024g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1519-931T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49649681 | ||||||
| chr3:49650053
|
C | T | 6 | a0003c0004t0006g0029a0003c0004t0006g0030a0003c0004t0006g0031others(3): Show | 6 | HG01516.hp1 HG01517.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1519-559C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49650053 | ||||||
| chr3:49650272
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1519-340G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49650272 | ||||||
| chr3:49650346
|
T | G | 155 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1519-266T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49650346 | ||||||
| chr3:49650348
|
G | A | 1 | a0014c0037t0025g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1519-264G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49650348 | ||||||
| chr3:49650425
|
T | C | 2 | a0003c0003t0014g0160a0003c0023t0014g0157 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1519-187T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49650425 | ||||||
| chr3:49650466
|
G | T | 1 | a0002c0002t0001g0167 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1519-146G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49650466 | ||||||
| chr3:49651240
|
G | A | 3 | a0001c0001t0002g0115a0001c0001t0002g0133a0001c0001t0002g0141 | 3 | HG00642.hp2 HG01168.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1986+161G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 4/11 | chr3 | 49651240 | ||||||
| chr3:49651394
|
G | A | 2 | a0001c0001t0002g0107a0015c0035t0002g0134 | 2 | NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1987-149G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 4/11 | chr3 | 49651394 | ||||||
| chr3:49651497
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0043others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1987-46G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 4/11 | chr3 | 49651497 | ||||||
| chr3:49658237
|
C | T | 1 | a0001c0001t0009g0149 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.8640+41C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49658237 | ||||||
| chr3:49658239
|
G | A | 3 | a0002c0002t0005g0062a0002c0002t0005g0074a0002c0002t0005g0075 | 3 | HG01081.hp1 HG01168.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.8640+43G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49658239 | ||||||
| chr3:49658364
|
C | G | 1 | a0003c0003t0004g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8640+168C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49658364 | ||||||
| chr3:49658657
|
A | C | 1 | a0003c0003t0004g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8640+461A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49658657 | ||||||
| chr3:49658742
|
C | T | 1 | a0001c0001t0012g0116 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.8640+546C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49658742 | ||||||
| chr3:49658762
|
T | C | 1 | a0002c0002t0001g0078 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.8640+566T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49658762 | ||||||
| chr3:49659200
|
C | G | 99 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.8640+1004C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49659200 | ||||||
| chr3:49659225
|
G | T | 1 | a0018c0031t0002g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.8640+1029G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49659225 | ||||||
| chr3:49659364
|
A | G | 54 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0055others(51): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.8641-1122A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49659364 | ||||||
| chr3:49659572
|
A | G | 1 | a0003c0004t0004g0024 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.8641-914A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49659572 | ||||||
| chr3:49659810
|
G | A | 6 | a0002c0002t0001g0180a0002c0002t0001g0181a0002c0002t0001g0182others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.8641-676G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49659810 | ||||||
| chr3:49659857
|
G | T | 6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.8641-629G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49659857 | ||||||
| chr3:49660026
|
G | A | 62 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0055others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.8641-460G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49660026 | ||||||
| chr3:49660289
|
C | G | 2 | a0003c0003t0014g0160a0003c0023t0014g0157 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.8641-197C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49660289 | ||||||
| chr3:49662646
|
C | T | 1 | a0002c0002t0001g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.10717+84C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 6/11 | chr3 | 49662646 | ||||||
| chr3:49663715
|
A | G | 1 | a0002c0002t0017g0058 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.11508+49A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 7/11 | chr3 | 49663715 | ||||||
| chr3:49664224
|
T | C | 1 | a0002c0002t0001g0076 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.11609-199T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 8/11 | chr3 | 49664224 | ||||||
| chr3:49664680
|
T | C | 6 | a0001c0001t0003g0041a0001c0001t0003g0122a0001c0001t0003g0128others(3): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.11741-119T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 9/11 | chr3 | 49664680 | ||||||
| chr3:49664897
|
C | T | 2 | a0003c0003t0014g0160a0003c0023t0014g0157 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.*14+44C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 10/11 | chr3 | 49664897 | ||||||
| chr3:49665051
|
T | C | 58 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0055others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.*15-178T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 10/11 | chr3 | 49665051 | ||||||
| chr3:49666643
|
G | A | 2 | a0007c0013t0013g0050a0007c0013t0013g0051 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.*105-947G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49666643 | ||||||
| chr3:49666644
|
A | G | 101 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.*105-946A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49666644 | ||||||
| chr3:49666649
|
G | A | 1 | a0001c0001t0009g0094 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.*105-941G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49666649 | ||||||
| chr3:49666684
|
G | A | 1 | a0003c0003t0004g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.*105-906G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49666684 | ||||||
| chr3:49666784
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.*105-806G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49666784 | ||||||
| chr3:49666899
|
G | GGGCTTCC others(3): Show |
6 | a0005c0007t0007g0002a0005c0007t0033g0005a0005c0007t0034g0004others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.*105-683_*105-674d others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 49666899 | |||||
| chr3:49667208
|
C | T | 1 | a0002c0002t0001g0172 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.*105-382C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49667208 | ||||||
| chr3:49667296
|
T | A | 99 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.*105-294T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49667296 | ||||||
| chr3:49667308
|
CA | C | 93 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.*105-264delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 49667308 | |||||
| chr3:49667554
|
T | C | 87 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0102others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.*105-36T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49667554 |