Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6597 |
|---|---|
| ensemblid | ENSG00000127616.22 |
| hgncid | 11100 |
| symbol | SMARCA4 |
| name | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 |
| refseq_nuc | NM_003072.5 |
| refseq_prot | NP_003063.2 |
| ensembl_nuc | ENST00000344626.10 |
| ensembl_prot | ENSP00000343896.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 10961030 |
| end | 11062273 |
| strand | + |
| ver | v1.2 |
| region | chr19:10961030-11062273 |
| region5000 | chr19:10956030-11067273 |
| regionname0 | SMARCA4_chr19_10961030_11062273 |
| regionname5000 | SMARCA4_chr19_10956030_11067273 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1647 | 282 | 69 | 47 | 117 | 9 | 38 | 87 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0002 | 0/0 | 1647 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0003 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0004 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4944 | 145 | 25 | 27 | 73 | 4 | 14 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0002 | 0/0 | 4944 | 39 | 5 | 7 | 25 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0003 | 0/0 | 4944 | 31 | 2 | 7 | 9 | 4 | 9 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0004 | 0/0 | 4944 | 18 | 14 | 0 | 3 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0005 | 0/0 | 4944 | 5 | 5 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0006 | 0/0 | 4944 | 4 | 4 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0007 | 0/0 | 4944 | 4 | 0 | 1 | 2 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0008 | 0/0 | 4944 | 3 | 3 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0009 | 0/0 | 4944 | 3 | 3 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0010 | 0/0 | 4944 | 3 | 0 | 3 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0011 | 0/0 | 4944 | 3 | 0 | 0 | 0 | 0 | 3 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0012 | 0/0 | 4944 | 2 | 0 | 0 | 0 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0013 | 0/0 | 4944 | 2 | 0 | 1 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0014 | 0/0 | 4944 | 2 | 0 | 1 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0015 | 0/0 | 4944 | 2 | 0 | 0 | 0 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0016 | 0/0 | 4944 | 2 | 2 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0017 | 0/0 | 4944 | 2 | 1 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0018 | 0/0 | 4944 | 2 | 0 | 0 | 2 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0019 | 0/0 | 4944 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0020 | 0/0 | 4944 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0021 | 0/0 | 4944 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0022 | 0/0 | 4944 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0023 | 0/0 | 4944 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0024 | 0/0 | 4944 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0025 | 0/0 | 4944 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0026 | 0/0 | 4944 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0027 | 0/0 | 4944 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0028 | 0/0 | 4944 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0029 | 0/0 | 4944 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0030 | 0/0 | 4944 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0031 | 0/0 | 4944 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| c0032 | 0/0 | 4944 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 634 | 283 | 69 | 47 | 117 | 10 | 38 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| t0002 | 0/0 | 634 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| t0003 | 0/0 | 634 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| t0004 | 0/0 | 634 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0117 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4944 | 145 | 25 | 27 | 73 | 4 | 14 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0002 | 0/0 | 4944 | 39 | 5 | 7 | 25 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0003 | 0/0 | 4944 | 31 | 2 | 7 | 9 | 4 | 9 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0004 | 0/0 | 4944 | 18 | 14 | 0 | 3 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0005 | 0/0 | 4944 | 5 | 5 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0006 | 0/0 | 4944 | 4 | 4 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0007 | 0/0 | 4944 | 4 | 0 | 1 | 2 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0008 | 0/0 | 4944 | 3 | 3 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0009 | 0/0 | 4944 | 3 | 3 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0010 | 0/0 | 4944 | 3 | 0 | 3 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0011 | 0/0 | 4944 | 3 | 0 | 0 | 0 | 0 | 3 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0012 | 0/0 | 4944 | 2 | 0 | 0 | 0 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0014 | 0/0 | 4944 | 2 | 0 | 1 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0015 | 0/0 | 4944 | 2 | 0 | 0 | 0 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0016 | 0/0 | 4944 | 2 | 2 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0017 | 0/0 | 4944 | 2 | 1 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0018 | 0/0 | 4944 | 2 | 0 | 0 | 2 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0019 | 0/0 | 4944 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0020 | 0/0 | 4944 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0021 | 0/0 | 4944 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0022 | 0/0 | 4944 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0024 | 0/0 | 4944 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0025 | 0/0 | 4944 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0026 | 0/0 | 4944 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0027 | 0/0 | 4944 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0028 | 0/0 | 4944 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0030 | 0/0 | 4944 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0031 | 0/0 | 4944 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0032 | 0/0 | 4944 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0002c0013 | 0/0 | 4944 | 2 | 0 | 1 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0003c0029 | 0/0 | 4944 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0004c0023 | 0/0 | 4944 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5577 | 143 | 25 | 26 | 72 | 4 | 14 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0001t0002 | 0/0 | 5577 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0001t0004 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0002t0001 | 0/0 | 5577 | 39 | 5 | 7 | 25 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0003t0001 | 0/0 | 5577 | 31 | 2 | 7 | 9 | 4 | 9 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0004t0001 | 0/0 | 5577 | 17 | 13 | 0 | 3 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0004t0003 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0005t0001 | 0/0 | 5577 | 5 | 5 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0006t0001 | 0/0 | 5577 | 4 | 4 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0007t0001 | 0/0 | 5577 | 4 | 0 | 1 | 2 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0008t0001 | 0/0 | 5577 | 3 | 3 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0009t0001 | 0/0 | 5577 | 3 | 3 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0010t0001 | 0/0 | 5577 | 3 | 0 | 3 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0011t0001 | 0/0 | 5577 | 3 | 0 | 0 | 0 | 0 | 3 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0012t0001 | 0/0 | 5577 | 2 | 0 | 0 | 0 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0014t0001 | 0/0 | 5577 | 2 | 0 | 1 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0015t0001 | 0/0 | 5577 | 2 | 0 | 0 | 0 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0016t0001 | 0/0 | 5577 | 2 | 2 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0017t0001 | 0/0 | 5577 | 2 | 1 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0018t0001 | 0/0 | 5577 | 2 | 0 | 0 | 2 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0019t0001 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0020t0001 | 0/0 | 5577 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0021t0001 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0022t0001 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0024t0001 | 0/0 | 5577 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0025t0001 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0026t0001 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0027t0001 | 0/0 | 5577 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0028t0001 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0030t0001 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0031t0001 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0001c0032t0001 | 0/0 | 5577 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0002c0013t0001 | 0/0 | 5577 | 2 | 0 | 1 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0003c0029t0001 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| a0004c0023t0001 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | copy fasta | chr19 | 10956030 | 11067273 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0117 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0004t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0005t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0005t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0005t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0005t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0006t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0006t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0006t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0006t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0007t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0007t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0007t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0007t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0008t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0008t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0008t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0009t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0009t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0009t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0010t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0010t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0010t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0011t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0011t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0011t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0012t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0012t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0014t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0014t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0015t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0015t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0016t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0016t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0017t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0017t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0018t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0018t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0019t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0020t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0021t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0022t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0024t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0025t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0026t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0027t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0028t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0030t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0031t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0001c0032t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0002c0013t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0002c0013t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0003c0029t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| a0004c0023t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0219 | EUR | GBR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00639 | hp2 | a0001 | c0014 | t0001 | g0235 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01069 | hp1 | a0001 | c0010 | t0001 | g0009 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01071 | hp2 | a0001 | c0010 | t0001 | g0010 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0218 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01109 | hp1 | a0001 | c0017 | t0001 | g0031 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0260 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0259 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0224 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01255 | hp1 | a0002 | c0013 | t0001 | g0019 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0245 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0206 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01358 | hp1 | a0001 | c0010 | t0001 | g0011 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | IBS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01515 | hp2 | a0001 | c0014 | t0001 | g0233 | EUR | IBS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0209 | EUR | IBS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01516 | hp2 | a0002 | c0013 | t0001 | g0016 | EUR | IBS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0243 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0257 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0216 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01981 | hp1 | a0001 | c0007 | t0001 | g0018 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0181 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0262 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02071 | hp2 | a0001 | c0007 | t0001 | g0020 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0214 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02083 | hp1 | a0001 | c0030 | t0001 | g0212 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02083 | hp2 | a0001 | c0004 | t0001 | g0079 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0131 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02135 | hp2 | a0001 | c0007 | t0001 | g0022 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02145 | hp1 | a0001 | c0004 | t0001 | g0160 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0203 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0025 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0139 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02280 | hp2 | a0001 | c0008 | t0001 | g0269 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0191 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02630 | hp1 | a0001 | c0009 | t0001 | g0003 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02647 | hp1 | a0001 | c0004 | t0001 | g0140 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0148 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02698 | hp1 | a0001 | c0011 | t0001 | g0276 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02698 | hp2 | a0001 | c0015 | t0001 | g0023 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0178 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02735 | hp2 | a0001 | c0007 | t0001 | g0017 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02738 | hp2 | a0001 | c0011 | t0001 | g0278 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02809 | hp1 | a0001 | c0006 | t0001 | g0267 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02809 | hp2 | a0004 | c0023 | t0001 | g0004 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0163 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02896 | hp2 | a0001 | c0006 | t0001 | g0272 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0128 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02897 | hp2 | a0001 | c0006 | t0001 | g0271 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02922 | hp2 | a0001 | c0028 | t0001 | g0007 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02965 | hp1 | a0001 | c0016 | t0001 | g0228 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02970 | hp1 | a0001 | c0016 | t0001 | g0230 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03041 | hp1 | a0001 | c0009 | t0001 | g0001 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03041 | hp2 | a0001 | c0008 | t0001 | g0266 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03098 | hp1 | a0001 | c0005 | t0001 | g0244 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0083 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03130 | hp1 | a0001 | c0021 | t0001 | g0175 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03139 | hp1 | a0001 | c0017 | t0001 | g0183 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0121 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0256 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03239 | hp1 | a0001 | c0004 | t0001 | g0005 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0237 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0082 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0273 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03491 | hp1 | a0001 | c0012 | t0001 | g0013 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03492 | hp1 | a0001 | c0012 | t0001 | g0015 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0154 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0211 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03669 | hp2 | a0001 | c0027 | t0001 | g0014 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0238 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03704 | hp1 | a0001 | c0032 | t0001 | g0231 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03704 | hp2 | a0001 | c0020 | t0001 | g0234 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03831 | hp1 | a0001 | c0015 | t0001 | g0021 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0210 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03942 | hp1 | a0001 | c0011 | t0001 | g0277 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0250 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0241 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0204 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG04204 | hp2 | a0001 | c0024 | t0001 | g0012 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18522 | hp1 | a0001 | c0004 | t0003 | g0180 | AFR | YRI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18522 | hp2 | a0001 | c0031 | t0001 | g0008 | AFR | YRI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18906 | hp2 | a0001 | c0008 | t0001 | g0270 | AFR | YRI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18940 | hp1 | a0001 | c0018 | t0001 | g0039 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0215 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18979 | hp1 | a0001 | c0019 | t0001 | g0192 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18983 | hp1 | a0003 | c0029 | t0001 | g0052 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18985 | hp1 | a0001 | c0003 | t0001 | g0253 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA18997 | hp2 | a0001 | c0018 | t0001 | g0157 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19000 | hp1 | a0001 | c0004 | t0001 | g0185 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0223 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | LWK | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | LWK | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19043 | hp2 | a0001 | c0004 | t0001 | g0167 | AFR | LWK | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19058 | hp2 | a0001 | c0022 | t0001 | g0201 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0072 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19079 | hp2 | a0001 | c0003 | t0001 | g0252 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19084 | hp2 | a0001 | c0003 | t0001 | g0258 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0138 | AFR | YRI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA20129 | hp1 | a0001 | c0026 | t0001 | g0281 | AFR | ASW | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA20129 | hp2 | a0001 | c0025 | t0001 | g0040 | AFR | ASW | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0225 | EUR | TSI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0137 | EUR | TSI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02109 | hp1 | a0001 | c0006 | t0001 | g0268 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0078 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02559 | hp1 | a0001 | c0009 | t0001 | g0002 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | USA | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | USA | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0118 | REF | REF | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0117 | REF | REF | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:10986435
|
A | T | 1 | a0003 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.602A>T | p.Gln201Leu | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 4/35 | 778/5577 | 602/4944 | 201/1647 | chr19 | 10986435 | ||
| chr19:10987920
|
T | C | 1 | a0002 | 2 | HG01255.hp1 HG01516.hp2 |
missense_variant | MODERATE | c.1114T>C | p.Tyr372His | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/35 | 1290/5577 | 1114/4944 | 372/1647 | chr19 | 10987920 | ||
| chr19:11059885
|
T | A | 1 | a0004 | 1 | HG02809.hp2 | missense_variant&splice_region_variant | MODERATE | c.4768T>A | p.Ser1590Thr | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/35 | 4944/5577 | 4768/4944 | 1590/1647 | chr19 | 11059885 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:10984205
|
G | A | 1 | a0001c0012 | 2 | HG03491.hp1 HG03492.hp1 |
synonymous_variant | LOW | c.54G>A | p.Pro18Pro | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/35 | 230/5577 | 54/4944 | 18/1647 | chr19 | 10984205 | ||
| chr19:10984271
|
C | T | 1 | a0001c0032 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.120C>T | p.His40His | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/35 | 296/5577 | 120/4944 | 40/1647 | chr19 | 10984271 | ||
| chr19:10985308
|
C | T | 1 | a0001c0031 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.258C>T | p.Asp86Asp | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 3/35 | 434/5577 | 258/4944 | 86/1647 | chr19 | 10985308 | ||
| chr19:10986424
|
C | T | 1 | a0001c0030 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.591C>T | p.Pro197Pro | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 4/35 | 767/5577 | 591/4944 | 197/1647 | chr19 | 10986424 | ||
| chr19:10987721
|
G | A | 2 | a0001c0006a0001c0008 | 7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
synonymous_variant | LOW | c.915G>A | p.Pro305Pro | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/35 | 1091/5577 | 915/4944 | 305/1647 | chr19 | 10987721 | ||
| chr19:10987736
|
C | A | 1 | a0001c0005 | 5 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
synonymous_variant | LOW | c.930C>A | p.Arg310Arg | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/35 | 1106/5577 | 930/4944 | 310/1647 | chr19 | 10987736 | ||
| chr19:10989338
|
C | T | 1 | a0001c0028 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1140C>T | p.His380His | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/35 | 1316/5577 | 1140/4944 | 380/1647 | chr19 | 10989338 | ||
| chr19:10989407
|
G | A | 1 | a0001c0019 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.1209G>A | p.Glu403Glu | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/35 | 1385/5577 | 1209/4944 | 403/1647 | chr19 | 10989407 | ||
| chr19:10991317
|
G | A | 2 | a0001c0009a0001c0010 | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
synonymous_variant | LOW | c.1413G>A | p.Lys471Lys | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/35 | 1589/5577 | 1413/4944 | 471/1647 | chr19 | 10991317 | ||
| chr19:10994917
|
A | G | 1 | a0001c0010 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
synonymous_variant | LOW | c.1509A>G | p.Ala503Ala | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/35 | 1685/5577 | 1509/4944 | 503/1647 | chr19 | 10994917 | ||
| chr19:10994932
|
T | C | 18 | a0001c0002a0001c0003a0001c0005others(15): Show | 107 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(104): Show |
synonymous_variant | LOW | c.1524T>C | p.His508His | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/35 | 1700/5577 | 1524/4944 | 508/1647 | chr19 | 10994932 | ||
| chr19:10994965
|
C | T | 1 | a0001c0018 | 2 | NA18940.hp1 NA18997.hp2 |
synonymous_variant | LOW | c.1557C>T | p.Asn519Asn | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/35 | 1733/5577 | 1557/4944 | 519/1647 | chr19 | 10994965 | ||
| chr19:10996359
|
A | G | 1 | a0001c0016 | 2 | HG02965.hp1 HG02970.hp1 |
synonymous_variant | LOW | c.1740A>G | p.Lys580Lys | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 10/35 | 1916/5577 | 1740/4944 | 580/1647 | chr19 | 10996359 | ||
| chr19:11013062
|
C | T | 2 | a0001c0011a0001c0027 | 4 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(1): Show |
synonymous_variant | LOW | c.2388C>T | p.Leu796Leu | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/35 | 2564/5577 | 2388/4944 | 796/1647 | chr19 | 11013062 | ||
| chr19:11021958
|
C | T | 1 | a0001c0026 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.2850C>T | p.Thr950Thr | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/35 | 3026/5577 | 2850/4944 | 950/1647 | chr19 | 11021958 | ||
| chr19:11024423
|
C | T | 1 | a0001c0020 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.3066C>T | p.Ser1022Ser | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/35 | 3242/5577 | 3066/4944 | 1022/1647 | chr19 | 11024423 | ||
| chr19:11033406
|
G | A | 1 | a0001c0021 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.3663G>A | p.Lys1221Lys | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 26/35 | 3839/5577 | 3663/4944 | 1221/1647 | chr19 | 11033406 | ||
| chr19:11034176
|
C | T | 1 | a0001c0025 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.3927C>T | p.His1309His | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 28/35 | 4103/5577 | 3927/4944 | 1309/1647 | chr19 | 11034176 | ||
| chr19:11035015
|
C | T | 4 | a0001c0007a0001c0012a0001c0015others(1): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
synonymous_variant | LOW | c.4053C>T | p.Asp1351Asp | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/35 | 4229/5577 | 4053/4944 | 1351/1647 | chr19 | 11035015 | ||
| chr19:11041363
|
A | G | 1 | a0001c0021 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.4227A>G | p.Ser1409Ser | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/35 | 4403/5577 | 4227/4944 | 1409/1647 | chr19 | 11041363 | ||
| chr19:11058324
|
C | T | 1 | a0001c0017 | 2 | HG01109.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.4494C>T | p.Tyr1498Tyr | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/35 | 4670/5577 | 4494/4944 | 1498/1647 | chr19 | 11058324 | ||
| chr19:11058838
|
C | T | 4 | a0001c0014a0001c0015a0001c0020others(1): Show | 6 | HG00639.hp2 HG01515.hp2 HG02698.hp2 others(3): Show |
synonymous_variant | LOW | c.4584C>T | p.Asp1528Asp | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/35 | 4760/5577 | 4584/4944 | 1528/1647 | chr19 | 11058838 | ||
| chr19:11059812
|
G | A | 1 | a0001c0022 | 1 | NA19058.hp2 | synonymous_variant | LOW | c.4695G>A | p.Glu1565Glu | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/35 | 4871/5577 | 4695/4944 | 1565/1647 | chr19 | 11059812 | ||
| chr19:11060163
|
T | C | 13 | a0001c0003a0001c0004a0001c0008others(10): Show | 69 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(66): Show |
synonymous_variant | LOW | c.4887T>C | p.Asp1629Asp | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/35 | 5063/5577 | 4887/4944 | 1629/1647 | chr19 | 11060163 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:10961061
|
C | T | 1 | a0001c0001t0004 | 1 | NA18957.hp2 | 5_prime_UTR_variant | MODIFIER | c.-145C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/35 | 23091 | chr19 | 10961061 | |||||
| chr19:11061817
|
G | T | 1 | a0001c0004t0003 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 35/35 | 1 | chr19 | 11061817 | |||||
| chr19:11062102
|
A | G | 1 | a0001c0001t0002 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*286A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 35/35 | 286 | chr19 | 11062102 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:10961242
|
G | A | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-32+68G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961242 | ||||||
| chr19:10961250
|
G | C | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-32+76G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961250 | ||||||
| chr19:10961336
|
G | T | 1 | a0001c0001t0001g0286 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-32+162G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961336 | ||||||
| chr19:10961337
|
T | G | 1 | a0001c0001t0001g0286 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-32+163T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961337 | ||||||
| chr19:10961458
|
G | T | 4 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(1): Show | 4 | NA18947.hp1 NA18957.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32+284G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961458 | ||||||
| chr19:10961516
|
C | T | 89 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(86): Show | 89 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.-32+342C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961516 | ||||||
| chr19:10961539
|
C | G | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-32+365C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961539 | ||||||
| chr19:10961560
|
G | C | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-32+386G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961560 | ||||||
| chr19:10961596
|
C | G | 1 | a0001c0001t0001g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-32+422C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961596 | ||||||
| chr19:10961647
|
C | T | 1 | a0001c0002t0001g0279 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-32+473C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961647 | ||||||
| chr19:10961674
|
G | A | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-32+500G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961674 | ||||||
| chr19:10961713
|
C | T | 1 | a0001c0019t0001g0192 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-32+539C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961713 | ||||||
| chr19:10961768
|
A | G | 4 | a0001c0001t0001g0275a0001c0011t0001g0276a0001c0011t0001g0277others(1): Show | 4 | HG02698.hp1 HG02738.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32+594A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961768 | ||||||
| chr19:10961802
|
T | C | 24 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0003t0001g0006others(21): Show | 24 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-32+628T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961802 | ||||||
| chr19:10961934
|
G | A | 112 | a0001c0001t0001g0024a0001c0001t0001g0193a0001c0001t0001g0194others(109): Show | 112 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.-32+760G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961934 | ||||||
| chr19:10961972
|
A | AT | 36 | a0001c0001t0001g0026a0001c0001t0001g0179a0001c0001t0001g0182others(33): Show | 36 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.-32+818dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10961972 | |||||
| chr19:10961972
|
A | ATT | 13 | a0001c0001t0001g0024a0001c0004t0001g0025a0001c0007t0001g0017others(10): Show | 13 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32+817_-32+818dup others(2): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10961972 | |||||
| chr19:10962310
|
A | G | 1 | a0001c0003t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-32+1136A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10962310 | ||||||
| chr19:10962325
|
CCTA | C | 13 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(10): Show | 13 | HG01081.hp1 HG01167.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32+1155_-32+1157d others(5): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10962325 | |||||
| chr19:10962541
|
G | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | HG02451.hp2 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+1367G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10962541 | ||||||
| chr19:10962657
|
C | T | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-32+1483C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10962657 | ||||||
| chr19:10962694
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-32+1520C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10962694 | ||||||
| chr19:10962764
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-32+1590A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10962764 | ||||||
| chr19:10962804
|
AAGTGCT | A | 12 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(9): Show | 12 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+1633_-32+1638d others(8): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10962804 | |||||
| chr19:10963178
|
A | T | 1 | a0001c0005t0001g0262 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-32+2004A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963178 | ||||||
| chr19:10963245
|
C | T | 1 | a0001c0024t0001g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-32+2071C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963245 | ||||||
| chr19:10963361
|
A | T | 1 | a0001c0021t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-32+2187A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963361 | ||||||
| chr19:10963370
|
C | CA | 31 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(28): Show | 31 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-32+2217dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10963370 | |||||
| chr19:10963370
|
CA | C | 9 | a0001c0001t0001g0030a0001c0001t0001g0173a0001c0002t0001g0174others(6): Show | 9 | HG01168.hp1 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32+2217delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10963370 | |||||
| chr19:10963396
|
A | G | 2 | a0001c0010t0001g0010a0001c0010t0001g0011 | 2 | HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-32+2222A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963396 | ||||||
| chr19:10963441
|
G | A | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-32+2267G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963441 | ||||||
| chr19:10963467
|
T | G | 2 | a0001c0017t0001g0031a0001c0017t0001g0183 | 2 | HG01109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-32+2293T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963467 | ||||||
| chr19:10963606
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-32+2432G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963606 | ||||||
| chr19:10963753
|
G | T | 1 | a0001c0001t0001g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-32+2579G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963753 | ||||||
| chr19:10963767
|
A | AT | 33 | a0001c0001t0001g0024a0001c0001t0001g0171a0001c0002t0001g0207others(30): Show | 33 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-32+2609dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10963767 | |||||
| chr19:10963767
|
A | ATT | 80 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(77): Show | 80 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-32+2608_-32+2609d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10963767 | |||||
| chr19:10964253
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-32+3079G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964253 | ||||||
| chr19:10964321
|
T | C | 6 | a0001c0003t0001g0006a0001c0010t0001g0009a0001c0010t0001g0010others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32+3147T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964321 | ||||||
| chr19:10964626
|
T | C | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG00408.hp1 NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-32+3452T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964626 | ||||||
| chr19:10964632
|
T | C | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-32+3458T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964632 | ||||||
| chr19:10964636
|
A | T | 114 | a0001c0001t0001g0024a0001c0001t0001g0193a0001c0001t0001g0194others(111): Show | 114 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.-32+3462A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964636 | ||||||
| chr19:10964691
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-32+3517C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964691 | ||||||
| chr19:10964738
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-32+3564C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964738 | ||||||
| chr19:10964837
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-32+3663T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964837 | ||||||
| chr19:10964884
|
G | A | 42 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0044others(39): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.-32+3710G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964884 | ||||||
| chr19:10964910
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-32+3736C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964910 | ||||||
| chr19:10965030
|
A | G | 166 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(163): Show | 166 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-32+3856A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965030 | ||||||
| chr19:10965073
|
C | T | 10 | a0001c0003t0001g0006a0001c0004t0001g0025a0001c0009t0001g0001others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32+3899C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965073 | ||||||
| chr19:10965284
|
A | T | 2 | a0001c0011t0001g0277a0001c0011t0001g0278 | 2 | HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-32+4110A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965284 | ||||||
| chr19:10965306
|
GC | G | 7 | a0001c0006t0001g0267a0001c0006t0001g0268a0001c0006t0001g0271others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32+4133delC | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965306 | ||||||
| chr19:10965511
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-32+4337C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965511 | ||||||
| chr19:10965516
|
A | G | 10 | a0001c0003t0001g0006a0001c0004t0001g0025a0001c0009t0001g0001others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32+4342A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965516 | ||||||
| chr19:10965722
|
G | C | 1 | a0001c0004t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-32+4548G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965722 | ||||||
| chr19:10965738
|
C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-32+4564C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965738 | ||||||
| chr19:10965823
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0171 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-32+4649T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965823 | ||||||
| chr19:10965970
|
G | GT | 39 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0142others(36): Show | 39 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.-32+4825dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10965970 | |||||
| chr19:10965970
|
G | GTT | 6 | a0001c0001t0001g0024a0001c0001t0001g0164a0001c0001t0001g0165others(3): Show | 6 | HG01081.hp2 HG01175.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32+4824_-32+4825d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10965970 | |||||
| chr19:10965970
|
GT | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(88): Show | 91 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.-32+4825delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10965970 | |||||
| chr19:10965970
|
GTT | G | 8 | a0001c0001t0001g0168a0001c0002t0001g0208a0001c0003t0001g0209others(5): Show | 8 | HG01168.hp2 HG01516.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32+4824_-32+4825d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10965970 | |||||
| chr19:10966323
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-32+5149G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966323 | ||||||
| chr19:10966355
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-32+5181C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966355 | ||||||
| chr19:10966403
|
C | A | 1 | a0001c0001t0004g0282 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-32+5229C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966403 | ||||||
| chr19:10966403
|
C | T | 2 | a0001c0002t0001g0172a0001c0002t0001g0174 | 2 | HG01074.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-32+5229C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966403 | ||||||
| chr19:10966557
|
C | T | 4 | a0001c0004t0001g0138a0001c0004t0001g0139a0001c0004t0001g0140others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32+5383C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966557 | ||||||
| chr19:10966652
|
G | A | 1 | a0001c0004t0001g0079 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-32+5478G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966652 | ||||||
| chr19:10966670
|
G | A | 90 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(87): Show | 90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.-32+5496G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966670 | ||||||
| chr19:10966761
|
G | A | 2 | a0001c0002t0001g0238a0001c0003t0001g0237 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-32+5587G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966761 | ||||||
| chr19:10966771
|
C | T | 12 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(9): Show | 12 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+5597C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966771 | ||||||
| chr19:10966986
|
G | A | 12 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(9): Show | 12 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+5812G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966986 | ||||||
| chr19:10967459
|
C | T | 74 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(71): Show | 74 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-32+6285C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10967459 | ||||||
| chr19:10967471
|
C | T | 1 | a0001c0021t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-32+6297C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10967471 | ||||||
| chr19:10967546
|
G | A | 1 | a0001c0003t0001g0211 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-32+6372G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10967546 | ||||||
| chr19:10967685
|
G | GT | 108 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0075others(105): Show | 108 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-32+6528dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10967685 | |||||
| chr19:10967685
|
G | GTT | 6 | a0001c0001t0001g0193a0001c0002t0001g0236a0001c0002t0001g0274others(3): Show | 6 | HG01069.hp1 HG01071.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32+6527_-32+6528d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10967685 | |||||
| chr19:10967858
|
A | AT | 12 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(9): Show | 12 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+6693dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10967858 | |||||
| chr19:10967867
|
T | A | 1 | a0001c0030t0001g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-32+6693T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10967867 | ||||||
| chr19:10967894
|
T | C | 1 | a0001c0011t0001g0276 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-32+6720T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10967894 | ||||||
| chr19:10967916
|
G | A | 1 | a0001c0004t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-32+6742G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10967916 | ||||||
| chr19:10968052
|
C | T | 11 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(8): Show | 11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+6878C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968052 | ||||||
| chr19:10968053
|
A | G | 12 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(9): Show | 12 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+6879A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968053 | ||||||
| chr19:10968071
|
T | A | 4 | a0001c0002t0001g0213a0001c0002t0001g0240a0001c0002t0001g0274others(1): Show | 4 | HG02040.hp2 HG02074.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32+6897T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968071 | ||||||
| chr19:10968150
|
C | T | 1 | a0001c0017t0001g0183 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-32+6976C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968150 | ||||||
| chr19:10968255
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-32+7081T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968255 | ||||||
| chr19:10968379
|
A | G | 2 | a0001c0001t0001g0136a0001c0003t0001g0137 | 2 | HG01255.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-32+7205A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968379 | ||||||
| chr19:10968456
|
G | A | 2 | a0001c0001t0001g0166a0001c0002t0001g0080 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-32+7282G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968456 | ||||||
| chr19:10968536
|
C | T | 5 | a0001c0002t0001g0257a0001c0003t0001g0206a0001c0014t0001g0233others(2): Show | 5 | HG00639.hp2 HG01261.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32+7362C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968536 | ||||||
| chr19:10968622
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-32+7448A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968622 | ||||||
| chr19:10968677
|
A | G | 2 | a0001c0002t0001g0172a0001c0002t0001g0174 | 2 | HG01074.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-32+7503A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968677 | ||||||
| chr19:10968785
|
C | T | 3 | a0001c0003t0001g0006a0001c0028t0001g0007a0001c0031t0001g0008 | 3 | HG02922.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-32+7611C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968785 | ||||||
| chr19:10968896
|
G | T | 3 | a0001c0003t0001g0006a0001c0028t0001g0007a0001c0031t0001g0008 | 3 | HG02922.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-32+7722G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968896 | ||||||
| chr19:10969006
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-32+7832G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969006 | ||||||
| chr19:10969054
|
C | T | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-32+7880C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969054 | ||||||
| chr19:10969153
|
A | C | 1 | a0001c0022t0001g0201 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-32+7979A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969153 | ||||||
| chr19:10969176
|
G | T | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-32+8002G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969176 | ||||||
| chr19:10969453
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-32+8279A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969453 | ||||||
| chr19:10969558
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-32+8384G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969558 | ||||||
| chr19:10969589
|
C | T | 1 | a0001c0022t0001g0201 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-32+8415C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969589 | ||||||
| chr19:10969762
|
C | T | 1 | a0001c0003t0001g0258 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-32+8588C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969762 | ||||||
| chr19:10969845
|
CATT | C | 11 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(8): Show | 11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+8674_-32+8676d others(5): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10969845 | |||||
| chr19:10970089
|
T | G | 3 | a0001c0002t0001g0238a0001c0003t0001g0237a0001c0003t0001g0241 | 3 | HG03239.hp2 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-32+8915T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970089 | ||||||
| chr19:10970245
|
C | T | 92 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(89): Show | 92 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-32+9071C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970245 | ||||||
| chr19:10970320
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-32+9146C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970320 | ||||||
| chr19:10970338
|
A | G | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-32+9164A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970338 | ||||||
| chr19:10970407
|
G | A | 6 | a0001c0001t0001g0186a0001c0004t0001g0082a0001c0004t0001g0083others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32+9233G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970407 | ||||||
| chr19:10970729
|
T | C | 87 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(84): Show | 87 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.-32+9555T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970729 | ||||||
| chr19:10970925
|
A | T | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-32+9751A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970925 | ||||||
| chr19:10970926
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-32+9752C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970926 | ||||||
| chr19:10971069
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-32+9895G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971069 | ||||||
| chr19:10971070
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-32+9896C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971070 | ||||||
| chr19:10971076
|
A | G | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32+9902A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971076 | ||||||
| chr19:10971150
|
C | T | 5 | a0001c0001t0001g0132a0001c0001t0001g0189a0001c0010t0001g0009others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+9976C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971150 | ||||||
| chr19:10971333
|
A | G | 85 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(82): Show | 85 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-32+10159A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971333 | ||||||
| chr19:10971400
|
T | C | 20 | a0001c0001t0001g0024a0001c0003t0001g0006a0001c0007t0001g0017others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-32+10226T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971400 | ||||||
| chr19:10971457
|
T | C | 12 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0084others(9): Show | 12 | HG00735.hp1 HG01167.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+10283T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971457 | ||||||
| chr19:10971490
|
CT | C | 11 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(8): Show | 11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+10332delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10971490 | |||||
| chr19:10971506
|
T | C | 1 | a0001c0006t0001g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-32+10332T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971506 | ||||||
| chr19:10971506
|
TC | T | 72 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(69): Show | 72 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-32+10333delC | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971506 | ||||||
| chr19:10971507
|
C | T | 18 | a0001c0001t0001g0275a0001c0002t0001g0207a0001c0002t0001g0263others(15): Show | 18 | HG02109.hp1 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-32+10333C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971507 | ||||||
| chr19:10971745
|
G | A | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-32+10571G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971745 | ||||||
| chr19:10971748
|
G | A | 11 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(8): Show | 11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+10574G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971748 | ||||||
| chr19:10971761
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-32+10587C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971761 | ||||||
| chr19:10971774
|
C | CT | 161 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(158): Show | 161 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.-32+10617dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10971774 | |||||
| chr19:10971795
|
G | A | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-32+10621G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971795 | ||||||
| chr19:10971796
|
G | T | 2 | a0001c0001t0001g0037a0001c0004t0001g0128 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-32+10622G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971796 | ||||||
| chr19:10971875
|
C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-32+10701C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971875 | ||||||
| chr19:10971913
|
T | C | 1 | a0001c0003t0001g0237 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-32+10739T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971913 | ||||||
| chr19:10971955
|
A | AT | 6 | a0001c0001t0001g0130a0001c0001t0001g0162a0001c0001t0001g0265others(3): Show | 6 | HG02074.hp1 HG02809.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32+10799dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10971955 | |||||
| chr19:10971955
|
A | ATT | 11 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(8): Show | 11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+10798_-32+1079 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10971955 | |||||
| chr19:10971955
|
AT | A | 8 | a0001c0001t0001g0032a0001c0005t0001g0243a0001c0005t0001g0244others(5): Show | 8 | HG00597.hp2 HG01515.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-32+10799delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10971955 | |||||
| chr19:10972111
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0189 | 2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-32+10937C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972111 | ||||||
| chr19:10972120
|
G | A | 2 | a0001c0001t0001g0088a0001c0002t0001g0146 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.-32+10946G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972120 | ||||||
| chr19:10972266
|
T | C | 11 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(8): Show | 11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+11092T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972266 | ||||||
| chr19:10972403
|
C | CT | 71 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(68): Show | 71 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.-32+11243dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10972403 | |||||
| chr19:10972534
|
G | T | 75 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(72): Show | 75 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-32+11360G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972534 | ||||||
| chr19:10972559
|
T | C | 1 | a0001c0003t0001g0215 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-32+11385T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972559 | ||||||
| chr19:10972595
|
G | C | 2 | a0001c0002t0001g0207a0001c0003t0001g0203 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-32+11421G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972595 | ||||||
| chr19:10972707
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-31-11414G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972707 | ||||||
| chr19:10972865
|
C | T | 22 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(19): Show | 22 | HG01081.hp1 HG01167.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31-11256C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972865 | ||||||
| chr19:10972895
|
G | T | 1 | a0001c0001t0001g0127 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-31-11226G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972895 | ||||||
| chr19:10972974
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-31-11147C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972974 | ||||||
| chr19:10973109
|
C | CA | 24 | a0001c0001t0001g0141a0001c0001t0001g0193a0001c0001t0001g0194others(21): Show | 24 | HG01081.hp1 HG01167.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.-31-10997dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10973109 | |||||
| chr19:10973359
|
G | T | 1 | a0001c0002t0001g0236 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-31-10762G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10973359 | ||||||
| chr19:10973401
|
G | T | 1 | a0001c0004t0001g0140 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-31-10720G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10973401 | ||||||
| chr19:10973407
|
C | CT | 10 | a0001c0001t0004g0282a0001c0003t0001g0006a0001c0009t0001g0001others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31-10701dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10973407 | |||||
| chr19:10973567
|
A | AT | 32 | a0001c0001t0001g0024a0001c0001t0001g0066a0001c0001t0001g0073others(29): Show | 32 | HG00639.hp2 HG01081.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.-31-10534dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10973567 | |||||
| chr19:10973821
|
T | C | 11 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(8): Show | 11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31-10300T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10973821 | ||||||
| chr19:10973865
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-31-10256C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10973865 | ||||||
| chr19:10974033
|
T | A | 2 | a0001c0002t0001g0045a0001c0002t0001g0070 | 2 | NA18980.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-31-10088T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974033 | ||||||
| chr19:10974228
|
A | G | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0161 | 3 | HG02257.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-31-9893A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974228 | ||||||
| chr19:10974318
|
A | G | 78 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(75): Show | 78 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-31-9803A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974318 | ||||||
| chr19:10974454
|
CT | C | 7 | a0001c0001t0001g0162a0001c0003t0001g0006a0001c0004t0001g0140others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31-9654delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974454 | |||||
| chr19:10974616
|
C | T | 2 | a0001c0004t0001g0121a0001c0004t0001g0160 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-31-9505C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974616 | ||||||
| chr19:10974617
|
G | A | 10 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(7): Show | 10 | HG00408.hp1 HG02080.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31-9504G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974617 | ||||||
| chr19:10974666
|
C | CAT | 27 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0046others(24): Show | 27 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.-31-9432_-31-9431d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974666 | |||||
| chr19:10974666
|
C | CATAT | 8 | a0001c0001t0001g0073a0001c0001t0001g0284a0001c0002t0001g0034others(5): Show | 8 | HG02145.hp2 HG03139.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31-9434_-31-9431d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974666 | |||||
| chr19:10974666
|
C | CATATAT | 6 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0033others(3): Show | 6 | HG01109.hp2 HG02976.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31-9436_-31-9431d others(8): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974666 | |||||
| chr19:10974667
|
A | G | 2 | a0001c0002t0001g0238a0001c0003t0001g0237 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-31-9454A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974667 | ||||||
| chr19:10974681
|
ATATATAT others(3): Show |
A | 1 | a0001c0006t0001g0271 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-31-9438_-31-9429d others(12): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974681 | |||||
| chr19:10974681
|
ATATATAT others(4): Show |
A | 2 | a0001c0006t0001g0267a0001c0006t0001g0272 | 2 | HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-31-9438_-31-9428d others(13): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974681 | |||||
| chr19:10974683
|
ATATATAT others(9): Show |
A | 2 | a0001c0007t0001g0020a0001c0007t0001g0022 | 2 | HG02071.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-31-9436_-31-9421d others(18): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974683 | |||||
| chr19:10974685
|
ATATATTT others(9): Show |
A | 8 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0012t0001g0013others(5): Show | 8 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-31-9434_-31-9419d others(18): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974685 | |||||
| chr19:10974685
|
ATATATTT others(10): Show |
A | 1 | a0001c0001t0001g0024 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-31-9434_-31-9418d others(19): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974685 | |||||
| chr19:10974688
|
TA | T | 8 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0135others(5): Show | 8 | HG01358.hp2 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-31-9432delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974688 | ||||||
| chr19:10974689
|
A | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0126a0001c0001t0001g0159 | 3 | HG01243.hp1 HG03471.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-31-9432A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974689 | ||||||
| chr19:10974689
|
AT | A | 65 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0041others(62): Show | 65 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.-31-9397delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974689 | |||||
| chr19:10974689
|
ATT | A | 38 | a0001c0001t0001g0036a0001c0001t0001g0076a0001c0001t0001g0086others(35): Show | 38 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.-31-9398_-31-9397d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974689 | |||||
| chr19:10974689
|
ATTT | A | 14 | a0001c0001t0001g0102a0001c0001t0001g0193a0001c0001t0001g0194others(11): Show | 14 | HG01081.hp1 HG01099.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-31-9399_-31-9397d others(5): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974689 | |||||
| chr19:10974689
|
ATTTT | A | 9 | a0001c0001t0001g0050a0001c0002t0001g0232a0001c0005t0001g0243others(6): Show | 9 | HG01884.hp2 HG01928.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31-9400_-31-9397d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974689 | |||||
| chr19:10974690
|
T | TA | 22 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0059others(19): Show | 22 | HG00099.hp1 HG00408.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31-9431_-31-9430i others(3): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974690 | ||||||
| chr19:10974690
|
T | TATA | 12 | a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0066others(9): Show | 12 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-31-9431_-31-9430i others(5): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974690 | ||||||
| chr19:10974690
|
T | TATATATA others(4): Show |
2 | a0001c0009t0001g0001a0001c0009t0001g0002 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-31-9431_-31-9430i others(13): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974690 | ||||||
| chr19:10974690
|
T | TATATATA others(6): Show |
1 | a0001c0009t0001g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-31-9431_-31-9430i others(15): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974690 | ||||||
| chr19:10974691
|
T | A | 73 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(70): Show | 73 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.-31-9430T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974691 | ||||||
| chr19:10974692
|
T | A | 76 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0043others(73): Show | 76 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-31-9429T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974692 | ||||||
| chr19:10974693
|
T | A | 89 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(86): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-31-9428T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974693 | ||||||
| chr19:10974694
|
T | A | 56 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0059others(53): Show | 56 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-31-9427T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974694 | ||||||
| chr19:10974695
|
T | A | 59 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(56): Show | 59 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-31-9426T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974695 | ||||||
| chr19:10974696
|
T | A | 16 | a0001c0001t0001g0051a0001c0001t0001g0095a0001c0001t0001g0122others(13): Show | 16 | HG01074.hp1 HG01168.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-31-9425T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974696 | ||||||
| chr19:10974697
|
T | A | 15 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0048others(12): Show | 15 | HG00639.hp1 HG01928.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31-9424T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974697 | ||||||
| chr19:10974698
|
T | A | 4 | a0001c0001t0001g0142a0001c0001t0001g0283a0001c0001t0001g0286others(1): Show | 4 | HG02738.hp1 NA18979.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31-9423T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974698 | ||||||
| chr19:10974699
|
T | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0067 | 3 | HG01928.hp2 NA18747.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-31-9422T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974699 | ||||||
| chr19:10974700
|
T | A | 2 | a0001c0001t0001g0283a0001c0025t0001g0040 | 2 | NA18979.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-31-9421T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974700 | ||||||
| chr19:10974701
|
T | A | 1 | a0001c0001t0001g0050 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-31-9420T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974701 | ||||||
| chr19:10974784
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | NA18971.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-31-9337G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974784 | ||||||
| chr19:10974867
|
T | C | 115 | a0001c0001t0001g0024a0001c0001t0001g0193a0001c0001t0001g0194others(112): Show | 115 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.-31-9254T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974867 | ||||||
| chr19:10974914
|
C | T | 94 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(91): Show | 94 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.-31-9207C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974914 | ||||||
| chr19:10974925
|
C | T | 1 | a0001c0003t0001g0154 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-31-9196C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974925 | ||||||
| chr19:10974986
|
C | A | 1 | a0001c0004t0001g0079 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-31-9135C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974986 | ||||||
| chr19:10975000
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-31-9121A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10975000 | ||||||
| chr19:10975017
|
C | CT | 12 | a0001c0001t0001g0029a0001c0001t0001g0101a0001c0001t0001g0106others(9): Show | 12 | HG01175.hp1 HG01192.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-31-9082dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10975017 | |||||
| chr19:10975017
|
CT | C | 25 | a0001c0001t0001g0068a0001c0001t0001g0077a0001c0001t0001g0086others(22): Show | 25 | HG00558.hp2 HG01071.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-31-9082delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10975017 | |||||
| chr19:10975079
|
G | A | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-31-9042G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10975079 | ||||||
| chr19:10975318
|
C | CT | 26 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(23): Show | 26 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.-31-8785dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10975318 | |||||
| chr19:10975318
|
CT | C | 11 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0110others(8): Show | 11 | HG00099.hp1 HG01515.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31-8785delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10975318 | |||||
| chr19:10975542
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-31-8579C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10975542 | ||||||
| chr19:10975897
|
G | A | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-31-8224G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10975897 | ||||||
| chr19:10975913
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-31-8208A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10975913 | ||||||
| chr19:10976070
|
T | C | 9 | a0001c0003t0001g0006a0001c0009t0001g0001a0001c0009t0001g0002others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-8051T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976070 | ||||||
| chr19:10976097
|
C | T | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-31-8024C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976097 | ||||||
| chr19:10976576
|
C | T | 5 | a0001c0002t0001g0254a0001c0002t0001g0261a0001c0006t0001g0267others(2): Show | 5 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31-7545C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976576 | ||||||
| chr19:10976577
|
G | A | 2 | a0001c0001t0001g0029a0001c0005t0001g0078 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-31-7544G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976577 | ||||||
| chr19:10976619
|
T | C | 2 | a0001c0016t0001g0228a0001c0016t0001g0230 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-31-7502T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976619 | ||||||
| chr19:10976630
|
G | A | 11 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(8): Show | 11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31-7491G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976630 | ||||||
| chr19:10976673
|
C | T | 2 | a0001c0018t0001g0039a0001c0018t0001g0157 | 2 | NA18940.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.-31-7448C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976673 | ||||||
| chr19:10976710
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-31-7411C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976710 | ||||||
| chr19:10976753
|
C | CAA | 124 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(121): Show | 124 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-31-7353_-31-7352d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10976753 | |||||
| chr19:10976753
|
C | CAAA | 47 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0044others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-31-7354_-31-7352d others(5): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10976753 | |||||
| chr19:10976770
|
T | G | 172 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(169): Show | 172 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.-31-7351T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976770 | ||||||
| chr19:10976852
|
T | C | 20 | a0001c0001t0001g0024a0001c0003t0001g0006a0001c0007t0001g0017others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-31-7269T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976852 | ||||||
| chr19:10976866
|
G | A | 1 | a0001c0004t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-31-7255G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976866 | ||||||
| chr19:10976920
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-31-7201G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976920 | ||||||
| chr19:10976971
|
C | T | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-31-7150C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976971 | ||||||
| chr19:10977120
|
T | C | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-31-7001T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977120 | ||||||
| chr19:10977123
|
C | A | 9 | a0001c0003t0001g0006a0001c0009t0001g0001a0001c0009t0001g0002others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-6998C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977123 | ||||||
| chr19:10977214
|
G | A | 7 | a0001c0006t0001g0267a0001c0006t0001g0268a0001c0006t0001g0271others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31-6907G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977214 | ||||||
| chr19:10977252
|
T | C | 1 | a0001c0002t0001g0255 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-31-6869T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977252 | ||||||
| chr19:10977543
|
T | C | 170 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(167): Show | 170 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.-31-6578T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977543 | ||||||
| chr19:10977631
|
C | A | 11 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(8): Show | 11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31-6490C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977631 | ||||||
| chr19:10977797
|
C | T | 3 | a0001c0003t0001g0006a0001c0028t0001g0007a0001c0031t0001g0008 | 3 | HG02922.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-31-6324C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977797 | ||||||
| chr19:10977830
|
G | T | 3 | a0001c0003t0001g0006a0001c0028t0001g0007a0001c0031t0001g0008 | 3 | HG02922.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-31-6291G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977830 | ||||||
| chr19:10978042
|
C | G | 5 | a0001c0001t0001g0275a0001c0011t0001g0276a0001c0011t0001g0277others(2): Show | 5 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31-6079C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978042 | ||||||
| chr19:10978048
|
C | T | 3 | a0001c0007t0001g0018a0002c0013t0001g0016a0002c0013t0001g0019 | 3 | HG01255.hp1 HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-31-6073C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978048 | ||||||
| chr19:10978187
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0170 | 2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-31-5934C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978187 | ||||||
| chr19:10978622
|
G | A | 1 | a0001c0010t0001g0011 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-31-5499G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978622 | ||||||
| chr19:10978780
|
A | AAT | 3 | a0001c0001t0001g0081a0001c0001t0001g0111a0001c0001t0001g0133 | 3 | HG01071.hp1 HG01981.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-31-5324_-31-5323d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10978780 | |||||
| chr19:10978782
|
T | A | 9 | a0001c0001t0001g0030a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-5339T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978782 | ||||||
| chr19:10978784
|
T | A | 2 | a0001c0001t0001g0196a0001c0010t0001g0011 | 2 | HG01358.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-31-5337T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978784 | ||||||
| chr19:10978963
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-31-5158A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978963 | ||||||
| chr19:10979009
|
G | A | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-31-5112G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979009 | ||||||
| chr19:10979079
|
A | G | 1 | a0001c0001t0001g0283 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-31-5042A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979079 | ||||||
| chr19:10979119
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-31-5002G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979119 | ||||||
| chr19:10979125
|
T | C | 2 | a0001c0018t0001g0039a0001c0018t0001g0157 | 2 | NA18940.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.-31-4996T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979125 | ||||||
| chr19:10979170
|
G | A | 54 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(51): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.-31-4951G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979170 | ||||||
| chr19:10979343
|
A | G | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-31-4778A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979343 | ||||||
| chr19:10979412
|
C | CT | 12 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0284others(9): Show | 12 | HG01071.hp2 HG01358.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-31-4693dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10979412 | |||||
| chr19:10979412
|
CT | C | 7 | a0001c0001t0001g0056a0001c0001t0001g0076a0001c0001t0001g0147others(4): Show | 7 | HG01069.hp2 HG02965.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31-4693delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10979412 | |||||
| chr19:10979463
|
GCTCACTG others(29): Show |
G | 2 | a0001c0008t0001g0269a0001c0008t0001g0270 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-31-4654_-31-4619d others(38): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10979463 | |||||
| chr19:10979533
|
T | A | 2 | a0001c0004t0001g0167a0004c0023t0001g0004 | 2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-31-4588T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979533 | ||||||
| chr19:10979678
|
A | G | 3 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG01167.hp2 HG01943.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-31-4443A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979678 | ||||||
| chr19:10979968
|
C | T | 1 | a0001c0002t0001g0247 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-31-4153C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979968 | ||||||
| chr19:10980036
|
A | G | 9 | a0001c0003t0001g0006a0001c0009t0001g0001a0001c0009t0001g0002others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-4085A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10980036 | ||||||
| chr19:10980072
|
A | G | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-31-4049A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10980072 | ||||||
| chr19:10980165
|
C | T | 9 | a0001c0003t0001g0006a0001c0009t0001g0001a0001c0009t0001g0002others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-3956C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10980165 | ||||||
| chr19:10980223
|
T | C | 7 | a0001c0006t0001g0267a0001c0006t0001g0268a0001c0006t0001g0271others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31-3898T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10980223 | ||||||
| chr19:10980558
|
C | A | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-31-3563C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10980558 | ||||||
| chr19:10980633
|
CA | C | 276 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(273): Show | 276 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.-31-3475delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10980633 | |||||
| chr19:10980733
|
G | T | 4 | a0001c0004t0001g0138a0001c0004t0001g0139a0001c0004t0001g0140others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-3388G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10980733 | ||||||
| chr19:10981032
|
G | A | 1 | a0001c0021t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-31-3089G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981032 | ||||||
| chr19:10981052
|
G | C | 1 | a0001c0016t0001g0230 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-31-3069G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981052 | ||||||
| chr19:10981400
|
C | G | 3 | a0001c0006t0001g0267a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG02809.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-31-2721C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981400 | ||||||
| chr19:10981463
|
G | A | 9 | a0001c0003t0001g0006a0001c0009t0001g0001a0001c0009t0001g0002others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-2658G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981463 | ||||||
| chr19:10981585
|
C | G | 2 | a0001c0016t0001g0228a0001c0016t0001g0230 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-31-2536C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981585 | ||||||
| chr19:10981711
|
C | T | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-31-2410C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981711 | ||||||
| chr19:10981988
|
C | G | 11 | a0001c0001t0001g0024a0001c0007t0001g0017a0001c0007t0001g0018others(8): Show | 11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31-2133C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981988 | ||||||
| chr19:10982028
|
G | A | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-31-2093G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982028 | ||||||
| chr19:10982066
|
C | T | 1 | a0001c0002t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-31-2055C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982066 | ||||||
| chr19:10982175
|
A | C | 1 | a0001c0001t0001g0068 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-31-1946A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982175 | ||||||
| chr19:10982456
|
A | G | 1 | a0001c0001t0001g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-31-1665A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982456 | ||||||
| chr19:10982502
|
C | CT | 18 | a0001c0001t0001g0033a0001c0001t0001g0044a0001c0001t0001g0050others(15): Show | 18 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.-31-1604dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10982502 | |||||
| chr19:10982502
|
CT | C | 7 | a0001c0002t0001g0254a0001c0002t0001g0261a0001c0009t0001g0001others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31-1604delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10982502 | |||||
| chr19:10982530
|
T | C | 7 | a0001c0003t0001g0260a0001c0009t0001g0001a0001c0009t0001g0002others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31-1591T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982530 | ||||||
| chr19:10982555
|
G | A | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-31-1566G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982555 | ||||||
| chr19:10982568
|
C | T | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-31-1553C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982568 | ||||||
| chr19:10982583
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-31-1538G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982583 | ||||||
| chr19:10982656
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-31-1465T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982656 | ||||||
| chr19:10982692
|
G | A | 75 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(72): Show | 75 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-31-1429G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982692 | ||||||
| chr19:10983103
|
A | G | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-31-1018A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983103 | ||||||
| chr19:10983145
|
A | T | 2 | a0001c0002t0001g0220a0001c0003t0001g0223 | 2 | NA18939.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-31-976A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983145 | ||||||
| chr19:10983200
|
T | C | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31-921T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983200 | ||||||
| chr19:10983395
|
T | G | 2 | a0001c0002t0001g0207a0001c0003t0001g0203 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-31-726T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983395 | ||||||
| chr19:10983433
|
G | GT | 9 | a0001c0001t0001g0164a0001c0001t0001g0186a0001c0002t0001g0274others(6): Show | 9 | HG01109.hp1 HG01175.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-671dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10983433 | |||||
| chr19:10983503
|
G | A | 2 | a0001c0004t0001g0167a0004c0023t0001g0004 | 2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-31-618G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983503 | ||||||
| chr19:10983537
|
C | T | 1 | a0001c0018t0001g0157 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-31-584C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983537 | ||||||
| chr19:10983818
|
C | T | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31-303C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983818 | ||||||
| chr19:10983900
|
G | A | 1 | a0001c0005t0001g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-31-221G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983900 | ||||||
| chr19:10983915
|
C | T | 4 | a0001c0004t0001g0138a0001c0004t0001g0139a0001c0004t0001g0140others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-206C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983915 | ||||||
| chr19:10984107
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-31-14G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10984107 | ||||||
| chr19:10984492
|
T | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0158 | 2 | HG01884.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.222+119T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10984492 | ||||||
| chr19:10984804
|
C | G | 1 | a0001c0001t0001g0047 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.222+431C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10984804 | ||||||
| chr19:10985034
|
T | C | 19 | a0001c0003t0001g0006a0001c0007t0001g0017a0001c0007t0001g0018others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.223-239T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985034 | ||||||
| chr19:10985096
|
C | T | 2 | a0001c0004t0001g0072a0001c0004t0001g0185 | 2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.223-177C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985096 | ||||||
| chr19:10985154
|
G | A | 1 | a0001c0003t0001g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.223-119G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985154 | ||||||
| chr19:10985155
|
C | T | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.223-118C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985155 | ||||||
| chr19:10985181
|
G | A | 1 | a0001c0004t0001g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.223-92G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985181 | ||||||
| chr19:10985220
|
T | C | 19 | a0001c0003t0001g0006a0001c0007t0001g0017a0001c0007t0001g0018others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.223-53T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985220 | ||||||
| chr19:10985231
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0171 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.223-42G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985231 | ||||||
| chr19:10985700
|
C | G | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+295C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 3/34 | chr19 | 10985700 | ||||||
| chr19:10985934
|
C | T | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.356-255C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 3/34 | chr19 | 10985934 | ||||||
| chr19:10986151
|
T | C | 1 | a0001c0003t0001g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.356-38T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 3/34 | chr19 | 10986151 | ||||||
| chr19:10986175
|
A | G | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.356-14A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 3/34 | chr19 | 10986175 | ||||||
| chr19:10986667
|
C | T | 2 | a0001c0002t0001g0220a0001c0003t0001g0223 | 2 | NA18939.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.760+74C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 4/34 | chr19 | 10986667 | ||||||
| chr19:10986709
|
G | A | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.760+116G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 4/34 | chr19 | 10986709 | ||||||
| chr19:10986774
|
C | T | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.761-131C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 4/34 | chr19 | 10986774 | ||||||
| chr19:10986869
|
C | T | 2 | a0001c0008t0001g0269a0001c0008t0001g0270 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.761-36C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 4/34 | chr19 | 10986869 | ||||||
| chr19:10987033
|
C | T | 4 | a0001c0011t0001g0276a0001c0011t0001g0277a0001c0011t0001g0278others(1): Show | 4 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.859+30C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987033 | ||||||
| chr19:10987034
|
G | A | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.859+31G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987034 | ||||||
| chr19:10987094
|
G | T | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.859+91G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987094 | ||||||
| chr19:10987096
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.859+93C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987096 | ||||||
| chr19:10987131
|
T | C | 3 | a0001c0007t0001g0018a0002c0013t0001g0016a0002c0013t0001g0019 | 3 | HG01255.hp1 HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.859+128T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987131 | ||||||
| chr19:10987146
|
C | T | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.859+143C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987146 | ||||||
| chr19:10987178
|
G | A | 2 | a0001c0002t0001g0080a0001c0002t0001g0239 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.859+175G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987178 | ||||||
| chr19:10987475
|
C | T | 1 | a0001c0032t0001g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.860-191C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987475 | ||||||
| chr19:10987633
|
A | G | 1 | a0001c0027t0001g0014 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.860-33A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987633 | ||||||
| chr19:10988124
|
CT | C | 10 | a0001c0001t0001g0063a0001c0001t0001g0129a0001c0008t0001g0266others(7): Show | 10 | HG02698.hp1 HG02738.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1118+213delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chr19 | 10988124 | |||||
| chr19:10988607
|
G | T | 2 | a0001c0002t0001g0207a0001c0003t0001g0203 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1118+683G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10988607 | ||||||
| chr19:10988780
|
C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1119-537C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10988780 | ||||||
| chr19:10988933
|
C | T | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1119-384C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10988933 | ||||||
| chr19:10989040
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1119-277C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10989040 | ||||||
| chr19:10989047
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1119-270C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10989047 | ||||||
| chr19:10989089
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1119-228C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10989089 | ||||||
| chr19:10989099
|
A | G | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1119-218A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10989099 | ||||||
| chr19:10989303
|
G | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1119-14G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10989303 | ||||||
| chr19:10989702
|
T | TC | 7 | a0001c0007t0001g0018a0001c0007t0001g0020a0001c0007t0001g0022others(4): Show | 7 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1245+262dupC | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr19 | 10989702 | |||||
| chr19:10989705
|
C | CT | 103 | a0001c0001t0001g0048a0001c0001t0001g0095a0001c0001t0001g0100others(100): Show | 103 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1245+277dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr19 | 10989705 | |||||
| chr19:10989705
|
CT | C | 19 | a0001c0001t0001g0033a0001c0001t0001g0044a0001c0001t0001g0050others(16): Show | 19 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.1245+277delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr19 | 10989705 | |||||
| chr19:10989706
|
T | C | 3 | a0001c0007t0001g0017a0001c0012t0001g0013a0001c0012t0001g0015 | 3 | HG02735.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1245+263T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10989706 | ||||||
| chr19:10989726
|
C | CA | 6 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(3): Show | 6 | NA18941.hp1 NA18942.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245+284dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr19 | 10989726 | |||||
| chr19:10989784
|
C | T | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1245+341C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10989784 | ||||||
| chr19:10989785
|
A | G | 16 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(13): Show | 16 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.1245+342A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10989785 | ||||||
| chr19:10989952
|
C | T | 4 | a0001c0011t0001g0276a0001c0011t0001g0277a0001c0011t0001g0278others(1): Show | 4 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1245+509C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10989952 | ||||||
| chr19:10990000
|
G | C | 1 | a0001c0001t0001g0060 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1245+557G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990000 | ||||||
| chr19:10990058
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1245+615C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990058 | ||||||
| chr19:10990097
|
C | T | 1 | a0001c0007t0001g0020 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1245+654C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990097 | ||||||
| chr19:10990312
|
C | T | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1246-838C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990312 | ||||||
| chr19:10990329
|
A | C | 7 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0103others(4): Show | 7 | NA18747.hp1 NA18948.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.1246-821A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990329 | ||||||
| chr19:10990435
|
G | A | 1 | a0001c0003t0001g0217 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1246-715G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990435 | ||||||
| chr19:10990553
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1246-597C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990553 | ||||||
| chr19:10990633
|
G | A | 1 | a0001c0002t0001g0249 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1246-517G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990633 | ||||||
| chr19:10990633
|
G | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0100 | 2 | HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1246-517G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990633 | ||||||
| chr19:10990757
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1246-393C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990757 | ||||||
| chr19:10990883
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1246-267C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990883 | ||||||
| chr19:10990943
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1246-207A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990943 | ||||||
| chr19:10991007
|
G | A | 4 | a0001c0004t0001g0138a0001c0004t0001g0139a0001c0004t0001g0140others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1246-143G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10991007 | ||||||
| chr19:10991084
|
C | T | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1246-66C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10991084 | ||||||
| chr19:10991124
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1246-26C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10991124 | ||||||
| chr19:10991331
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0158 | 2 | HG01884.hp1 HG01952.hp1 |
splice_region_variant&intron_variant | LOW | c.1419+8C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10991331 | ||||||
| chr19:10991466
|
T | C | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1419+143T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10991466 | ||||||
| chr19:10991496
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1419+173T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10991496 | ||||||
| chr19:10991543
|
G | T | 1 | a0001c0001t0001g0186 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1419+220G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10991543 | ||||||
| chr19:10991920
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0126others(1): Show | 4 | HG01975.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1419+597G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10991920 | ||||||
| chr19:10992086
|
G | T | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1419+763G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992086 | ||||||
| chr19:10992391
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1419+1068G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992391 | ||||||
| chr19:10992420
|
A | AT | 27 | a0001c0001t0001g0044a0001c0001t0001g0122a0001c0001t0001g0126others(24): Show | 27 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1419+1118dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr19 | 10992420 | |||||
| chr19:10992420
|
A | T | 1 | a0001c0001t0001g0129 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1419+1097A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992420 | ||||||
| chr19:10992420
|
AT | A | 6 | a0001c0001t0001g0114a0001c0001t0004g0282a0001c0010t0001g0009others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1419+1118delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr19 | 10992420 | |||||
| chr19:10992456
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1419+1133C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992456 | ||||||
| chr19:10992573
|
C | T | 1 | a0001c0002t0001g0255 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1419+1250C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992573 | ||||||
| chr19:10992784
|
T | C | 2 | a0001c0025t0001g0040a0001c0026t0001g0281 | 2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1419+1461T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992784 | ||||||
| chr19:10992834
|
G | A | 14 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(11): Show | 14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1419+1511G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992834 | ||||||
| chr19:10992878
|
A | G | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1419+1555A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992878 | ||||||
| chr19:10992942
|
A | G | 1 | a0001c0020t0001g0234 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1419+1619A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992942 | ||||||
| chr19:10992984
|
C | CT | 6 | a0001c0001t0001g0145a0001c0002t0001g0208a0001c0002t0001g0263others(3): Show | 6 | HG01192.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1419+1680dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr19 | 10992984 | |||||
| chr19:10992984
|
CT | C | 11 | a0001c0001t0001g0089a0001c0001t0001g0110a0001c0001t0001g0126others(8): Show | 11 | HG01975.hp1 HG02040.hp2 HG03490.hp2 others(8): Show |
intron_variant | MODIFIER | c.1419+1680delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr19 | 10992984 | |||||
| chr19:10993081
|
G | A | 1 | a0001c0002t0001g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1420-1747G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10993081 | ||||||
| chr19:10993132
|
T | G | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1420-1696T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10993132 | ||||||
| chr19:10993337
|
T | C | 1 | a0001c0004t0001g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1420-1491T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10993337 | ||||||
| chr19:10993445
|
C | T | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1420-1383C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10993445 | ||||||
| chr19:10993560
|
C | T | 5 | a0001c0005t0001g0078a0001c0005t0001g0243a0001c0005t0001g0244others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1420-1268C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10993560 | ||||||
| chr19:10993690
|
C | G | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1420-1138C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10993690 | ||||||
| chr19:10994071
|
A | G | 107 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(104): Show | 107 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1420-757A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994071 | ||||||
| chr19:10994215
|
G | A | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1420-613G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994215 | ||||||
| chr19:10994318
|
G | GT | 52 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0038others(49): Show | 52 | HG00544.hp1 HG00544.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1420-487dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr19 | 10994318 | |||||
| chr19:10994318
|
GT | G | 6 | a0001c0001t0001g0176a0001c0001t0001g0284a0001c0002t0001g0208others(3): Show | 6 | HG02698.hp2 HG02809.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1420-487delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr19 | 10994318 | |||||
| chr19:10994328
|
T | G | 31 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0046others(28): Show | 31 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1420-500T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994328 | ||||||
| chr19:10994346
|
C | G | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1420-482C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994346 | ||||||
| chr19:10994468
|
C | T | 2 | a0001c0008t0001g0269a0001c0008t0001g0270 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1420-360C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994468 | ||||||
| chr19:10994543
|
C | T | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1420-285C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994543 | ||||||
| chr19:10994710
|
CT | C | 6 | a0001c0011t0001g0276a0001c0011t0001g0277a0001c0011t0001g0278others(3): Show | 6 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.1420-117delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994710 | ||||||
| chr19:10995189
|
C | G | 7 | a0001c0006t0001g0267a0001c0006t0001g0268a0001c0006t0001g0271others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1593+188C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995189 | ||||||
| chr19:10995216
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1593+215C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995216 | ||||||
| chr19:10995243
|
G | A | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1593+242G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995243 | ||||||
| chr19:10995376
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1593+375C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995376 | ||||||
| chr19:10995626
|
T | C | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1594-587T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995626 | ||||||
| chr19:10995672
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1594-541G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995672 | ||||||
| chr19:10995924
|
C | T | 103 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(100): Show | 103 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.1594-289C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995924 | ||||||
| chr19:10996078
|
C | T | 3 | a0001c0006t0001g0267a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG02809.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1594-135C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10996078 | ||||||
| chr19:10996114
|
T | C | 113 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(110): Show | 113 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1594-99T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10996114 | ||||||
| chr19:10996409
|
G | A | 5 | a0001c0002t0001g0207a0001c0003t0001g0203a0001c0010t0001g0009others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1761+29G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 10/34 | chr19 | 10996409 | ||||||
| chr19:10996457
|
T | C | 111 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(108): Show | 111 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1762-37T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 10/34 | chr19 | 10996457 | ||||||
| chr19:10996458
|
G | A | 7 | a0001c0006t0001g0267a0001c0006t0001g0268a0001c0006t0001g0271others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1762-36G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 10/34 | chr19 | 10996458 | ||||||
| chr19:10996619
|
G | A | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1812+75G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10996619 | ||||||
| chr19:10996920
|
T | C | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1812+376T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10996920 | ||||||
| chr19:10996994
|
T | G | 4 | a0001c0011t0001g0276a0001c0011t0001g0277a0001c0011t0001g0278others(1): Show | 4 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1812+450T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10996994 | ||||||
| chr19:10996996
|
C | T | 1 | a0001c0032t0001g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1812+452C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10996996 | ||||||
| chr19:10997093
|
C | T | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1812+549C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997093 | ||||||
| chr19:10997111
|
G | A | 14 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(11): Show | 14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1812+567G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997111 | ||||||
| chr19:10997159
|
A | T | 1 | a0001c0001t0001g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1812+615A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997159 | ||||||
| chr19:10997433
|
C | T | 1 | a0001c0002t0001g0273 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1812+889C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997433 | ||||||
| chr19:10997447
|
TC | T | 35 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0046others(32): Show | 35 | HG00438.hp2 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1812+906delC | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 10997447 | |||||
| chr19:10997518
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1812+974G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997518 | ||||||
| chr19:10997617
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1812+1073C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997617 | ||||||
| chr19:10997620
|
C | T | 1 | a0001c0015t0001g0023 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1812+1076C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997620 | ||||||
| chr19:10997693
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1812+1149C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997693 | ||||||
| chr19:10997847
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1812+1303A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997847 | ||||||
| chr19:10997891
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1812+1347C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997891 | ||||||
| chr19:10998062
|
T | G | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1812+1518T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998062 | ||||||
| chr19:10998328
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1812+1784C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998328 | ||||||
| chr19:10998329
|
G | A | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1812+1785G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998329 | ||||||
| chr19:10998503
|
C | CTTT | 13 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(10): Show | 13 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1812+1972_1812+197 others(7): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 10998503 | |||||
| chr19:10998521
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1812+1977C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998521 | ||||||
| chr19:10998792
|
A | G | 14 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(11): Show | 14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1812+2248A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998792 | ||||||
| chr19:10998839
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1812+2295T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998839 | ||||||
| chr19:10998948
|
C | T | 2 | a0001c0001t0001g0166a0001c0003t0001g0006 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1812+2404C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998948 | ||||||
| chr19:10999022
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1812+2478C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10999022 | ||||||
| chr19:10999046
|
G | C | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1812+2502G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10999046 | ||||||
| chr19:10999308
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1812+2764G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10999308 | ||||||
| chr19:10999414
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1812+2870T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10999414 | ||||||
| chr19:10999993
|
A | G | 2 | a0001c0025t0001g0040a0001c0026t0001g0281 | 2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1813-3036A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10999993 | ||||||
| chr19:11000048
|
A | C | 1 | a0001c0001t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1813-2981A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11000048 | ||||||
| chr19:11000227
|
CA | C | 17 | a0001c0001t0001g0098a0001c0002t0001g0232a0001c0002t0001g0239others(14): Show | 17 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1813-2787delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11000227 | |||||
| chr19:11000407
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1813-2622A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11000407 | ||||||
| chr19:11000676
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1813-2353C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11000676 | ||||||
| chr19:11000739
|
C | T | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1813-2290C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11000739 | ||||||
| chr19:11000803
|
G | A | 2 | a0001c0002t0001g0057a0001c0002t0001g0058 | 2 | HG01069.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1813-2226G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11000803 | ||||||
| chr19:11000841
|
C | CA | 92 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(89): Show | 92 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1813-2187dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11000841 | |||||
| chr19:11000859
|
C | CA | 17 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0059others(14): Show | 17 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.1813-2153dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11000859 | |||||
| chr19:11000878
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1813-2151T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11000878 | ||||||
| chr19:11001167
|
A | G | 14 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(11): Show | 14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1813-1862A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001167 | ||||||
| chr19:11001475
|
C | T | 109 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(106): Show | 109 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1813-1554C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001475 | ||||||
| chr19:11001477
|
T | A | 109 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(106): Show | 109 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1813-1552T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001477 | ||||||
| chr19:11001658
|
C | G | 17 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(14): Show | 17 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1813-1371C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001658 | ||||||
| chr19:11001659
|
T | TGACCCTC | 17 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(14): Show | 17 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1813-1370_1813-136 others(11): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001659 | ||||||
| chr19:11001758
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0004t0001g0128others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1813-1271G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001758 | ||||||
| chr19:11001765
|
T | C | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1813-1264T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001765 | ||||||
| chr19:11001814
|
C | T | 6 | a0001c0001t0001g0186a0001c0004t0001g0082a0001c0004t0001g0083others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1813-1215C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001814 | ||||||
| chr19:11002007
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0155 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1813-1022A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002007 | ||||||
| chr19:11002280
|
C | T | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1813-749C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002280 | ||||||
| chr19:11002281
|
T | C | 14 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(11): Show | 14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1813-748T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002281 | ||||||
| chr19:11002346
|
A | C | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1813-683A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002346 | ||||||
| chr19:11002351
|
C | T | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1813-678C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002351 | ||||||
| chr19:11002389
|
G | C | 1 | a0001c0017t0001g0183 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1813-640G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002389 | ||||||
| chr19:11002401
|
C | T | 6 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(3): Show | 6 | NA18941.hp1 NA18942.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.1813-628C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002401 | ||||||
| chr19:11002431
|
A | G | 11 | a0001c0002t0001g0080a0001c0002t0001g0232a0001c0002t0001g0239others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1813-598A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002431 | ||||||
| chr19:11002503
|
A | AAAAT | 14 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(11): Show | 14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1813-522_1813-519d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11002503 | |||||
| chr19:11002507
|
TA | T | 6 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1813-517delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11002507 | |||||
| chr19:11002534
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1813-495C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002534 | ||||||
| chr19:11002605
|
C | T | 4 | a0001c0011t0001g0276a0001c0011t0001g0277a0001c0011t0001g0278others(1): Show | 4 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1813-424C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002605 | ||||||
| chr19:11002799
|
CA | C | 81 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0093others(78): Show | 81 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1813-208delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11002799 | |||||
| chr19:11002799
|
CAA | C | 28 | a0001c0002t0001g0208a0001c0002t0001g0232a0001c0003t0001g0006others(25): Show | 28 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1813-209_1813-208d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11002799 | |||||
| chr19:11002819
|
A | G | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1813-210A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002819 | ||||||
| chr19:11002821
|
A | G | 2 | a0001c0016t0001g0228a0001c0016t0001g0230 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1813-208A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002821 | ||||||
| chr19:11002844
|
G | A | 14 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(11): Show | 14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1813-185G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002844 | ||||||
| chr19:11002975
|
T | C | 20 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.1813-54T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002975 | ||||||
| chr19:11003226
|
G | A | 73 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(70): Show | 73 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1943+67G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 12/34 | chr19 | 11003226 | ||||||
| chr19:11003321
|
G | T | 14 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(11): Show | 14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1944-19G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 12/34 | chr19 | 11003321 | ||||||
| chr19:11003328
|
C | T | 4 | a0001c0002t0001g0220a0001c0003t0001g0217a0001c0003t0001g0223others(1): Show | 4 | NA18939.hp2 NA18940.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1944-12C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 12/34 | chr19 | 11003328 | ||||||
| chr19:11003530
|
C | T | 68 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(65): Show | 68 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.2001+133C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003530 | ||||||
| chr19:11003531
|
G | T | 1 | a0001c0021t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2001+134G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003531 | ||||||
| chr19:11003537
|
G | A | 2 | a0001c0002t0001g0226a0001c0002t0001g0229 | 2 | NA18947.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2001+140G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003537 | ||||||
| chr19:11003676
|
A | G | 12 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0084others(9): Show | 12 | HG00735.hp1 HG01167.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.2001+279A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003676 | ||||||
| chr19:11003711
|
A | AT | 13 | a0001c0001t0001g0033a0001c0001t0001g0050a0001c0001t0001g0133others(10): Show | 13 | HG01928.hp2 HG01981.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2001+332dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11003711 | |||||
| chr19:11003711
|
A | T | 11 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(8): Show | 11 | HG01081.hp1 HG01167.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.2001+314A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003711 | ||||||
| chr19:11003799
|
C | A | 14 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(11): Show | 14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.2001+402C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003799 | ||||||
| chr19:11003815
|
A | C | 2 | a0001c0016t0001g0228a0001c0016t0001g0230 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2001+418A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003815 | ||||||
| chr19:11003915
|
T | C | 89 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(86): Show | 89 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.2001+518T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003915 | ||||||
| chr19:11004004
|
G | A | 2 | a0001c0002t0001g0207a0001c0003t0001g0203 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2001+607G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004004 | ||||||
| chr19:11004112
|
G | A | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2001+715G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004112 | ||||||
| chr19:11004173
|
T | C | 2 | a0001c0002t0001g0242a0001c0002t0001g0248 | 2 | HG02135.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2001+776T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004173 | ||||||
| chr19:11004248
|
T | C | 14 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(11): Show | 14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.2001+851T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004248 | ||||||
| chr19:11004253
|
AT | A | 99 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(96): Show | 99 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2001+870delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11004253 | |||||
| chr19:11004253
|
ATT | A | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2001+869_2001+870d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11004253 | |||||
| chr19:11004402
|
C | T | 14 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(11): Show | 14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.2001+1005C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004402 | ||||||
| chr19:11004431
|
A | G | 4 | a0001c0002t0001g0232a0001c0002t0001g0273a0001c0030t0001g0212others(1): Show | 4 | HG02083.hp1 HG03490.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.2001+1034A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004431 | ||||||
| chr19:11004634
|
A | G | 1 | a0001c0002t0001g0261 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2001+1237A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004634 | ||||||
| chr19:11004811
|
G | GT | 20 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2001+1422dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11004811 | |||||
| chr19:11004845
|
CT | C | 99 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(96): Show | 99 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2001+1460delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11004845 | |||||
| chr19:11004870
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0152 | 2 | HG00597.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2001+1473C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004870 | ||||||
| chr19:11004920
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2001+1523A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004920 | ||||||
| chr19:11004935
|
G | A | 4 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0265others(1): Show | 4 | HG00639.hp1 NA18954.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2001+1538G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004935 | ||||||
| chr19:11005116
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2001+1719G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005116 | ||||||
| chr19:11005331
|
T | C | 1 | a0001c0002t0001g0232 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2001+1934T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005331 | ||||||
| chr19:11005419
|
G | T | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2001+2022G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005419 | ||||||
| chr19:11005483
|
G | A | 20 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2001+2086G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005483 | ||||||
| chr19:11005590
|
C | T | 14 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0102others(11): Show | 14 | HG01099.hp1 HG01109.hp1 HG02970.hp2 others(11): Show |
intron_variant | MODIFIER | c.2001+2193C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005590 | ||||||
| chr19:11005619
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2001+2222T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005619 | ||||||
| chr19:11005929
|
A | G | 7 | a0001c0006t0001g0267a0001c0006t0001g0268a0001c0006t0001g0271others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002-1973A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005929 | ||||||
| chr19:11006232
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2002-1670G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006232 | ||||||
| chr19:11006276
|
C | T | 1 | a0001c0002t0001g0227 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2002-1626C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006276 | ||||||
| chr19:11006554
|
C | T | 2 | a0001c0002t0001g0207a0001c0003t0001g0203 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2002-1348C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006554 | ||||||
| chr19:11006570
|
A | G | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2002-1332A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006570 | ||||||
| chr19:11006581
|
T | A | 1 | a0001c0001t0001g0049 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2002-1321T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006581 | ||||||
| chr19:11006760
|
T | C | 20 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2002-1142T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006760 | ||||||
| chr19:11006895
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0087 | 2 | HG01167.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2002-1007G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006895 | ||||||
| chr19:11006949
|
T | C | 1 | a0001c0017t0001g0031 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2002-953T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006949 | ||||||
| chr19:11006951
|
A | G | 20 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2002-951A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006951 | ||||||
| chr19:11006979
|
C | T | 14 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(11): Show | 14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.2002-923C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006979 | ||||||
| chr19:11007140
|
C | T | 2 | a0001c0002t0001g0242a0001c0002t0001g0248 | 2 | HG02135.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2002-762C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11007140 | ||||||
| chr19:11007298
|
C | T | 2 | a0001c0012t0001g0013a0001c0012t0001g0015 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2002-604C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11007298 | ||||||
| chr19:11007375
|
C | T | 1 | a0001c0003t0001g0245 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2002-527C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11007375 | ||||||
| chr19:11007416
|
T | C | 3 | a0001c0002t0001g0238a0001c0003t0001g0237a0001c0003t0001g0241 | 3 | HG03239.hp2 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2002-486T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11007416 | ||||||
| chr19:11007429
|
C | CA | 17 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0101others(14): Show | 17 | HG00558.hp1 HG00621.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.2002-450dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11007429 | |||||
| chr19:11007429
|
CA | C | 22 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0067others(19): Show | 22 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.2002-450delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11007429 | |||||
| chr19:11007429
|
CAAAAAAA | C | 7 | a0001c0006t0001g0267a0001c0006t0001g0268a0001c0006t0001g0271others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002-456_2002-450d others(9): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11007429 | |||||
| chr19:11007808
|
A | C | 1 | a0001c0001t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2002-94A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11007808 | ||||||
| chr19:11007883
|
T | C | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2002-19T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11007883 | ||||||
| chr19:11008035
|
C | T | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2123+12C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008035 | ||||||
| chr19:11008085
|
T | A | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+62T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008085 | ||||||
| chr19:11008086
|
G | C | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+63G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008086 | ||||||
| chr19:11008087
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+64G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008087 | ||||||
| chr19:11008093
|
A | T | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+70A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008093 | ||||||
| chr19:11008094
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+71T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008094 | ||||||
| chr19:11008095
|
C | G | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+72C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008095 | ||||||
| chr19:11008097
|
C | G | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+74C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008097 | ||||||
| chr19:11008098
|
A | T | 1 | a0001c0001t0001g0101 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+75A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008098 | ||||||
| chr19:11008120
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0170 | 2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2123+97G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008120 | ||||||
| chr19:11008214
|
C | T | 1 | a0001c0002t0001g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2123+191C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008214 | ||||||
| chr19:11008518
|
G | A | 2 | a0001c0012t0001g0013a0001c0012t0001g0015 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2123+495G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008518 | ||||||
| chr19:11008540
|
G | A | 7 | a0001c0001t0001g0182a0001c0009t0001g0001a0001c0009t0001g0002others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.2123+517G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008540 | ||||||
| chr19:11008596
|
G | C | 158 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(155): Show | 158 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.2123+573G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008596 | ||||||
| chr19:11008616
|
C | T | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2123+593C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008616 | ||||||
| chr19:11008641
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2123+618C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008641 | ||||||
| chr19:11008659
|
G | T | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2123+636G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008659 | ||||||
| chr19:11008973
|
C | CA | 14 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0161others(11): Show | 14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.2123+964dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11008973 | |||||
| chr19:11008975
|
A | C | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2123+952A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008975 | ||||||
| chr19:11009007
|
C | CT | 13 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(10): Show | 13 | HG00408.hp2 HG02109.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.2123+1018dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
C | CTT | 23 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0033others(20): Show | 23 | HG00438.hp2 HG00673.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.2123+1017_2123+101 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
C | CTTT | 27 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0036others(24): Show | 27 | HG00597.hp1 HG00639.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.2123+1016_2123+101 others(7): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
C | CTTTT | 33 | a0001c0001t0001g0032a0001c0001t0001g0073a0001c0001t0001g0095others(30): Show | 33 | HG00597.hp2 HG00621.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.2123+1015_2123+101 others(8): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
C | CTTTTT | 18 | a0001c0001t0001g0056a0001c0001t0001g0097a0001c0001t0001g0101others(15): Show | 18 | HG01952.hp1 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2123+1014_2123+101 others(9): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
C | CTTTTTT | 6 | a0001c0001t0001g0037a0001c0001t0001g0115a0001c0001t0001g0162others(3): Show | 6 | HG02717.hp1 HG02897.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.2123+1013_2123+101 others(10): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
C | CTTTTTTT others(11): Show |
1 | a0001c0010t0001g0011 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2123+1001_2123+101 others(22): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
CT | C | 16 | a0001c0001t0001g0024a0001c0001t0001g0084a0001c0001t0001g0090others(13): Show | 16 | HG00438.hp1 HG00735.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.2123+1018delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
CTT | C | 30 | a0001c0001t0001g0042a0001c0001t0001g0077a0001c0001t0001g0081others(27): Show | 30 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.2123+1017_2123+101 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
CTTTTTTT others(1): Show |
C | 22 | a0001c0002t0001g0058a0001c0002t0001g0070a0001c0002t0001g0071others(19): Show | 22 | HG00544.hp2 HG01099.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.2123+1011_2123+101 others(12): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
CTTTTTTT others(2): Show |
C | 64 | a0001c0001t0001g0200a0001c0002t0001g0034a0001c0002t0001g0045others(61): Show | 64 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.2123+1010_2123+101 others(13): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
CTTTTTTT others(3): Show |
C | 5 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0007t0001g0017others(2): Show | 5 | HG02735.hp2 HG02922.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2123+1009_2123+101 others(14): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0099 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2123+1008_2123+101 others(15): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0026t0001g0281 | 3 | NA18906.hp1 NA19005.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2123+1006_2123+101 others(17): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0161 | 3 | HG02257.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2123+1005_2123+101 others(18): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009007
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2123+1001_2123+101 others(22): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | |||||
| chr19:11009120
|
C | T | 1 | a0001c0002t0001g0227 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2123+1097C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009120 | ||||||
| chr19:11009138
|
C | T | 1 | a0001c0003t0001g0131 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2123+1115C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009138 | ||||||
| chr19:11009278
|
C | T | 3 | a0001c0004t0001g0139a0001c0004t0001g0140a0001c0004t0001g0163 | 3 | HG02258.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2124-1103C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009278 | ||||||
| chr19:11009354
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2124-1027G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009354 | ||||||
| chr19:11009612
|
C | T | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0161 | 3 | HG02257.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2124-769C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009612 | ||||||
| chr19:11009687
|
C | CT | 15 | a0001c0001t0001g0051a0001c0001t0001g0142a0001c0001t0001g0284others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.2124-675dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009687 | |||||
| chr19:11009877
|
C | T | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2124-504C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009877 | ||||||
| chr19:11009934
|
A | C | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2124-447A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009934 | ||||||
| chr19:11009938
|
C | T | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2124-443C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009938 | ||||||
| chr19:11010007
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2124-374G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11010007 | ||||||
| chr19:11010261
|
C | T | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2124-120C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11010261 | ||||||
| chr19:11010323
|
G | A | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2124-58G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11010323 | ||||||
| chr19:11010649
|
A | G | 1 | a0001c0003t0001g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2274+118A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11010649 | ||||||
| chr19:11010735
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2274+204C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11010735 | ||||||
| chr19:11011003
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2274+472G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011003 | ||||||
| chr19:11011193
|
G | A | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2274+662G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011193 | ||||||
| chr19:11011287
|
C | A | 7 | a0001c0006t0001g0267a0001c0006t0001g0268a0001c0006t0001g0271others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2274+756C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011287 | ||||||
| chr19:11011343
|
G | C | 1 | a0001c0001t0001g0120 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2274+812G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011343 | ||||||
| chr19:11011394
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2274+863T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011394 | ||||||
| chr19:11011718
|
G | T | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2274+1187G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011718 | ||||||
| chr19:11011776
|
C | G | 2 | a0001c0004t0001g0072a0001c0004t0001g0185 | 2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.2275-1173C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011776 | ||||||
| chr19:11011824
|
T | A | 1 | a0001c0001t0001g0195 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2275-1125T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011824 | ||||||
| chr19:11011855
|
G | T | 11 | a0001c0002t0001g0080a0001c0002t0001g0232a0001c0002t0001g0239others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.2275-1094G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011855 | ||||||
| chr19:11011932
|
C | G | 4 | a0001c0011t0001g0276a0001c0011t0001g0277a0001c0011t0001g0278others(1): Show | 4 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2275-1017C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011932 | ||||||
| chr19:11012034
|
G | T | 8 | a0001c0002t0001g0247a0001c0002t0001g0251a0001c0003t0001g0211others(5): Show | 8 | HG00099.hp1 HG01074.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2275-915G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012034 | ||||||
| chr19:11012264
|
T | G | 1 | a0001c0011t0001g0276 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2275-685T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012264 | ||||||
| chr19:11012415
|
T | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0111a0001c0001t0001g0133 | 3 | HG01071.hp1 HG01981.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2275-534T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012415 | ||||||
| chr19:11012522
|
C | G | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2275-427C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012522 | ||||||
| chr19:11012722
|
G | A | 1 | a0001c0011t0001g0276 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2275-227G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012722 | ||||||
| chr19:11012736
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2275-213C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012736 | ||||||
| chr19:11012760
|
C | T | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2275-189C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012760 | ||||||
| chr19:11012911
|
G | A | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2275-38G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012911 | ||||||
| chr19:11012946
|
C | A | 1 | a0001c0001t0001g0176 | 1 | NA20805.hp2 | splice_region_variant&intron_variant | LOW | c.2275-3C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012946 | ||||||
| chr19:11013155
|
G | A | 1 | a0001c0007t0001g0017 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2438+43G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11013155 | ||||||
| chr19:11013161
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2438+49G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11013161 | ||||||
| chr19:11013419
|
C | G | 15 | a0001c0002t0001g0080a0001c0002t0001g0146a0001c0002t0001g0232others(12): Show | 15 | HG00544.hp2 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2438+307C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11013419 | ||||||
| chr19:11013794
|
C | G | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2438+682C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11013794 | ||||||
| chr19:11013976
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2438+864A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11013976 | ||||||
| chr19:11013976
|
A | T | 1 | a0001c0004t0001g0128 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2438+864A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11013976 | ||||||
| chr19:11014292
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2438+1180A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014292 | ||||||
| chr19:11014308
|
G | A | 1 | a0001c0005t0001g0243 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2438+1196G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014308 | ||||||
| chr19:11014511
|
C | T | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2438+1399C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014511 | ||||||
| chr19:11014540
|
C | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0176a0001c0027t0001g0014 | 3 | HG01099.hp1 HG03669.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2438+1428C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014540 | ||||||
| chr19:11014782
|
A | T | 1 | a0001c0003t0001g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2438+1670A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014782 | ||||||
| chr19:11014821
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0179 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2438+1709T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014821 | ||||||
| chr19:11014931
|
G | A | 5 | a0001c0001t0001g0186a0001c0004t0001g0082a0001c0004t0001g0083others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2438+1819G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014931 | ||||||
| chr19:11014961
|
C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2438+1849C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014961 | ||||||
| chr19:11015124
|
A | G | 3 | a0001c0003t0001g0006a0001c0028t0001g0007a0001c0031t0001g0008 | 3 | HG02922.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2438+2012A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015124 | ||||||
| chr19:11015237
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2438+2125G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015237 | ||||||
| chr19:11015284
|
T | C | 113 | a0001c0001t0001g0205a0001c0002t0001g0034a0001c0002t0001g0045others(110): Show | 113 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.2438+2172T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015284 | ||||||
| chr19:11015484
|
T | C | 8 | a0001c0002t0001g0247a0001c0002t0001g0251a0001c0003t0001g0211others(5): Show | 8 | HG00099.hp1 HG01074.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2438+2372T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015484 | ||||||
| chr19:11015521
|
T | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0111a0001c0001t0001g0133 | 3 | HG01071.hp1 HG01981.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2438+2409T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015521 | ||||||
| chr19:11015523
|
G | C | 75 | a0001c0001t0001g0205a0001c0002t0001g0034a0001c0002t0001g0045others(72): Show | 75 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.2438+2411G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015523 | ||||||
| chr19:11015589
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2438+2477C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015589 | ||||||
| chr19:11015597
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2438+2485C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015597 | ||||||
| chr19:11015604
|
C | T | 1 | a0001c0003t0001g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2438+2492C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015604 | ||||||
| chr19:11015967
|
T | C | 112 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(109): Show | 112 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.2438+2855T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015967 | ||||||
| chr19:11016007
|
T | G | 1 | a0001c0002t0001g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2438+2895T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016007 | ||||||
| chr19:11016393
|
G | T | 75 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(72): Show | 75 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.2439-2564G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016393 | ||||||
| chr19:11016422
|
T | C | 1 | a0001c0002t0001g0261 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2439-2535T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016422 | ||||||
| chr19:11016530
|
G | T | 1 | a0001c0001t0001g0056 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2439-2427G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016530 | ||||||
| chr19:11016551
|
G | T | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2439-2406G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016551 | ||||||
| chr19:11016700
|
T | C | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2439-2257T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016700 | ||||||
| chr19:11016729
|
T | A | 1 | a0001c0003t0001g0250 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2439-2228T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016729 | ||||||
| chr19:11016981
|
C | T | 2 | a0001c0002t0001g0273a0001c0032t0001g0231 | 2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2439-1976C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016981 | ||||||
| chr19:11017047
|
C | T | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2439-1910C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017047 | ||||||
| chr19:11017096
|
C | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0054others(1): Show | 4 | HG00408.hp2 NA19009.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.2439-1861C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017096 | ||||||
| chr19:11017136
|
C | T | 1 | a0001c0002t0001g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2439-1821C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017136 | ||||||
| chr19:11017243
|
G | A | 3 | a0001c0002t0001g0207a0001c0003t0001g0203a0001c0024t0001g0012 | 3 | HG02145.hp2 HG03453.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2439-1714G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017243 | ||||||
| chr19:11017257
|
G | C | 1 | a0001c0001t0001g0189 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2439-1700G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017257 | ||||||
| chr19:11017332
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2439-1625C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017332 | ||||||
| chr19:11017387
|
G | A | 8 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.2439-1570G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017387 | ||||||
| chr19:11017686
|
G | T | 1 | a0001c0017t0001g0031 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2439-1271G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017686 | ||||||
| chr19:11017689
|
C | T | 1 | a0001c0003t0001g0137 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2439-1268C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017689 | ||||||
| chr19:11017874
|
G | C | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2439-1083G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017874 | ||||||
| chr19:11017920
|
A | G | 157 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(154): Show | 157 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.2439-1037A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017920 | ||||||
| chr19:11018148
|
T | C | 113 | a0001c0001t0001g0205a0001c0002t0001g0034a0001c0002t0001g0045others(110): Show | 113 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.2439-809T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018148 | ||||||
| chr19:11018217
|
C | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0187 | 2 | NA18945.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2439-740C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018217 | ||||||
| chr19:11018264
|
G | A | 1 | a0001c0003t0001g0148 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2439-693G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018264 | ||||||
| chr19:11018293
|
C | T | 13 | a0001c0002t0001g0080a0001c0002t0001g0232a0001c0002t0001g0239others(10): Show | 13 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.2439-664C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018293 | ||||||
| chr19:11018425
|
G | A | 4 | a0001c0001t0001g0283a0001c0001t0001g0285a0001c0001t0004g0282others(1): Show | 4 | NA18947.hp1 NA18957.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.2439-532G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018425 | ||||||
| chr19:11018492
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2439-465C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018492 | ||||||
| chr19:11018604
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2439-353G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018604 | ||||||
| chr19:11018663
|
T | C | 8 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.2439-294T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018663 | ||||||
| chr19:11018753
|
C | G | 237 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(234): Show | 237 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.2439-204C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018753 | ||||||
| chr19:11018845
|
C | T | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2439-112C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018845 | ||||||
| chr19:11018924
|
C | T | 10 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0102others(7): Show | 10 | HG01099.hp1 HG03669.hp2 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.2439-33C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018924 | ||||||
| chr19:11019129
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2505+106C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 17/34 | chr19 | 11019129 | ||||||
| chr19:11019204
|
C | T | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2505+181C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 17/34 | chr19 | 11019204 | ||||||
| chr19:11019438
|
G | A | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2506-153G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 17/34 | chr19 | 11019438 | ||||||
| chr19:11019519
|
G | A | 22 | a0001c0002t0001g0080a0001c0002t0001g0207a0001c0002t0001g0232others(19): Show | 22 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.2506-72G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 17/34 | chr19 | 11019519 | ||||||
| chr19:11019755
|
G | A | 2 | a0001c0001t0001g0026a0001c0024t0001g0012 | 2 | HG01109.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2616+54G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11019755 | ||||||
| chr19:11019759
|
C | T | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2616+58C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11019759 | ||||||
| chr19:11019766
|
C | T | 4 | a0001c0004t0001g0138a0001c0004t0001g0139a0001c0004t0001g0140others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2616+65C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11019766 | ||||||
| chr19:11019833
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2616+132C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11019833 | ||||||
| chr19:11020057
|
A | T | 1 | a0001c0002t0001g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2616+356A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020057 | ||||||
| chr19:11020415
|
G | GT | 8 | a0001c0001t0001g0065a0001c0001t0001g0152a0001c0001t0001g0196others(5): Show | 8 | HG00597.hp1 NA18953.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.2616+727dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | INFO_REALIGN_3_PRIME | chr19 | 11020415 | |||||
| chr19:11020513
|
C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2616+812C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020513 | ||||||
| chr19:11020546
|
G | T | 4 | a0001c0002t0001g0208a0001c0011t0001g0276a0001c0011t0001g0277others(1): Show | 4 | HG02698.hp1 HG02738.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2616+845G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020546 | ||||||
| chr19:11020564
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0265 | 2 | NA18954.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2616+863C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020564 | ||||||
| chr19:11020599
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2616+898T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020599 | ||||||
| chr19:11020674
|
C | T | 2 | a0001c0006t0001g0271a0001c0006t0001g0272 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2616+973C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020674 | ||||||
| chr19:11020727
|
T | C | 8 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.2617-998T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020727 | ||||||
| chr19:11021260
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2617-465G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11021260 | ||||||
| chr19:11021404
|
G | A | 74 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(71): Show | 74 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2617-321G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11021404 | ||||||
| chr19:11021504
|
G | T | 2 | a0001c0006t0001g0271a0001c0006t0001g0272 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2617-221G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11021504 | ||||||
| chr19:11021639
|
G | A | 28 | a0001c0002t0001g0080a0001c0002t0001g0146a0001c0002t0001g0207others(25): Show | 28 | HG00544.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.2617-86G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11021639 | ||||||
| chr19:11021721
|
G | A | 1 | a0001c0002t0001g0249 | 1 | HG00621.hp1 | splice_region_variant&intron_variant | LOW | c.2617-4G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11021721 | ||||||
| chr19:11022049
|
C | T | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2859+82C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11022049 | ||||||
| chr19:11022249
|
A | C | 30 | a0001c0002t0001g0080a0001c0002t0001g0146a0001c0002t0001g0207others(27): Show | 30 | HG00544.hp2 HG01884.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.2859+282A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11022249 | ||||||
| chr19:11022380
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2859+413G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11022380 | ||||||
| chr19:11022596
|
A | G | 112 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(109): Show | 112 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.2859+629A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11022596 | ||||||
| chr19:11022643
|
C | G | 1 | a0001c0001t0001g0097 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2859+676C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11022643 | ||||||
| chr19:11022655
|
C | T | 1 | a0001c0005t0001g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2859+688C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11022655 | ||||||
| chr19:11023017
|
C | T | 2 | a0001c0002t0001g0238a0001c0003t0001g0237 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2860-501C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11023017 | ||||||
| chr19:11023043
|
A | G | 31 | a0001c0001t0001g0153a0001c0002t0001g0080a0001c0002t0001g0146others(28): Show | 31 | HG00544.hp2 HG01884.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.2860-475A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11023043 | ||||||
| chr19:11023151
|
C | T | 14 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0084others(11): Show | 14 | HG00735.hp1 HG01167.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.2860-367C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11023151 | ||||||
| chr19:11023282
|
C | T | 3 | a0001c0011t0001g0276a0001c0011t0001g0277a0001c0011t0001g0278 | 3 | HG02698.hp1 HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2860-236C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11023282 | ||||||
| chr19:11023414
|
A | G | 65 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(62): Show | 65 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.2860-104A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11023414 | ||||||
| chr19:11023752
|
G | C | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2973+121G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 20/34 | chr19 | 11023752 | ||||||
| chr19:11024011
|
A | G | 1 | a0001c0004t0001g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2974-320A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 20/34 | chr19 | 11024011 | ||||||
| chr19:11024018
|
T | C | 75 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(72): Show | 75 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.2974-313T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 20/34 | chr19 | 11024018 | ||||||
| chr19:11024024
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0126a0001c0001t0001g0155 | 3 | HG03490.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2974-307C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 20/34 | chr19 | 11024024 | ||||||
| chr19:11024076
|
G | A | 5 | a0001c0002t0001g0257a0001c0003t0001g0206a0001c0014t0001g0233others(2): Show | 5 | HG00639.hp2 HG01261.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2974-255G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 20/34 | chr19 | 11024076 | ||||||
| chr19:11024102
|
G | C | 1 | a0001c0010t0001g0011 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2974-229G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 20/34 | chr19 | 11024102 | ||||||
| chr19:11024612
|
A | C | 1 | a0001c0003t0001g0250 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3081+174A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11024612 | ||||||
| chr19:11024613
|
G | C | 1 | a0001c0003t0001g0250 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3081+175G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11024613 | ||||||
| chr19:11024649
|
G | T | 1 | a0001c0003t0001g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3081+211G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11024649 | ||||||
| chr19:11024978
|
T | C | 155 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(152): Show | 155 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.3082-444T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11024978 | ||||||
| chr19:11024992
|
C | G | 1 | a0001c0001t0001g0284 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3082-430C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11024992 | ||||||
| chr19:11024993
|
G | C | 1 | a0001c0001t0001g0284 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3082-429G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11024993 | ||||||
| chr19:11025339
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3082-83C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11025339 | ||||||
| chr19:11025539
|
C | G | 158 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(155): Show | 158 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.3168+31C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025539 | ||||||
| chr19:11025566
|
G | A | 1 | a0001c0003t0001g0219 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3168+58G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025566 | ||||||
| chr19:11025628
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0159 | 2 | HG01243.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3168+120T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025628 | ||||||
| chr19:11025639
|
C | T | 150 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(147): Show | 150 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.3168+131C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025639 | ||||||
| chr19:11025663
|
A | G | 1 | a0001c0011t0001g0278 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3168+155A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025663 | ||||||
| chr19:11025671
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0047a0001c0001t0001g0073 | 3 | HG00597.hp2 NA18995.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.3168+163C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025671 | ||||||
| chr19:11025776
|
T | G | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3168+268T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025776 | ||||||
| chr19:11025777
|
C | T | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3168+269C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025777 | ||||||
| chr19:11025833
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3168+325C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025833 | ||||||
| chr19:11025939
|
T | G | 2 | a0001c0011t0001g0277a0001c0011t0001g0278 | 2 | HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.3169-361T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025939 | ||||||
| chr19:11026106
|
G | C | 1 | a0001c0001t0001g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3169-194G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11026106 | ||||||
| chr19:11026181
|
C | T | 64 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(61): Show | 64 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.3169-119C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11026181 | ||||||
| chr19:11026183
|
T | G | 1 | a0001c0001t0001g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3169-117T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11026183 | ||||||
| chr19:11026184
|
G | C | 1 | a0001c0001t0001g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3169-116G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11026184 | ||||||
| chr19:11026459
|
T | C | 11 | a0001c0004t0001g0005a0001c0007t0001g0017a0001c0007t0001g0018others(8): Show | 11 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.3215+113T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026459 | ||||||
| chr19:11026497
|
C | CT | 65 | a0001c0001t0001g0084a0001c0001t0001g0109a0001c0001t0001g0110others(62): Show | 65 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.3215+170dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr19 | 11026497 | |||||
| chr19:11026497
|
CT | C | 57 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(54): Show | 57 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.3215+170delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr19 | 11026497 | |||||
| chr19:11026666
|
T | G | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3215+320T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026666 | ||||||
| chr19:11026753
|
C | G | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3215+407C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026753 | ||||||
| chr19:11026755
|
T | C | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3215+409T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026755 | ||||||
| chr19:11026756
|
C | T | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3215+410C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026756 | ||||||
| chr19:11026777
|
G | T | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3215+431G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026777 | ||||||
| chr19:11026788
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3215+442C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026788 | ||||||
| chr19:11026794
|
C | T | 2 | a0001c0025t0001g0040a0001c0026t0001g0281 | 2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3215+448C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026794 | ||||||
| chr19:11026810
|
A | G | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3215+464A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026810 | ||||||
| chr19:11026898
|
C | T | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3215+552C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026898 | ||||||
| chr19:11026899
|
T | C | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3215+553T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026899 | ||||||
| chr19:11027491
|
G | C | 155 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(152): Show | 155 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.3216-293G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11027491 | ||||||
| chr19:11027550
|
T | C | 63 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(60): Show | 63 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.3216-234T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11027550 | ||||||
| chr19:11027616
|
A | G | 11 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(8): Show | 11 | HG01109.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.3216-168A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11027616 | ||||||
| chr19:11028055
|
C | T | 1 | a0001c0003t0001g0203 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3382+105C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028055 | ||||||
| chr19:11028199
|
G | C | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3382+249G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028199 | ||||||
| chr19:11028406
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3382+456C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028406 | ||||||
| chr19:11028632
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3382+682C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028632 | ||||||
| chr19:11028665
|
G | A | 1 | a0001c0003t0001g0137 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3382+715G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028665 | ||||||
| chr19:11028772
|
G | C | 2 | a0001c0002t0001g0208a0001c0028t0001g0007 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3382+822G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028772 | ||||||
| chr19:11028842
|
C | G | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3382+892C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028842 | ||||||
| chr19:11028960
|
G | T | 153 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(150): Show | 153 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.3382+1010G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028960 | ||||||
| chr19:11028980
|
C | G | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.3382+1030C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028980 | ||||||
| chr19:11028981
|
T | G | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.3382+1031T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028981 | ||||||
| chr19:11029057
|
C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3382+1107C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029057 | ||||||
| chr19:11029070
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0187 | 2 | NA18945.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.3382+1120A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029070 | ||||||
| chr19:11029220
|
G | A | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3382+1270G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029220 | ||||||
| chr19:11029468
|
A | G | 64 | a0001c0001t0001g0205a0001c0002t0001g0034a0001c0002t0001g0045others(61): Show | 64 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.3383-1262A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029468 | ||||||
| chr19:11029593
|
G | A | 1 | a0001c0030t0001g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3383-1137G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029593 | ||||||
| chr19:11029723
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3383-1007G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029723 | ||||||
| chr19:11029755
|
C | T | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0161 | 3 | HG02257.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3383-975C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029755 | ||||||
| chr19:11029818
|
C | T | 1 | a0001c0020t0001g0234 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3383-912C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029818 | ||||||
| chr19:11029917
|
C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3383-813C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029917 | ||||||
| chr19:11029972
|
G | A | 2 | a0001c0003t0001g0006a0001c0031t0001g0008 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3383-758G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029972 | ||||||
| chr19:11029991
|
C | T | 3 | a0001c0001t0001g0119a0001c0001t0001g0156a0001c0001t0001g0165 | 3 | HG00621.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.3383-739C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029991 | ||||||
| chr19:11030027
|
T | C | 157 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(154): Show | 157 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.3383-703T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11030027 | ||||||
| chr19:11030543
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3383-187G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11030543 | ||||||
| chr19:11030605
|
C | T | 2 | a0001c0003t0001g0006a0001c0031t0001g0008 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3383-125C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11030605 | ||||||
| chr19:11030669
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3383-61G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11030669 | ||||||
| chr19:11030677
|
C | T | 3 | a0001c0002t0001g0238a0001c0003t0001g0237a0001c0003t0001g0241 | 3 | HG03239.hp2 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3383-53C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11030677 | ||||||
| chr19:11031070
|
C | T | 1 | a0001c0003t0001g0211 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3546+177C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11031070 | ||||||
| chr19:11031348
|
C | T | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3546+455C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11031348 | ||||||
| chr19:11031768
|
G | C | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3546+875G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11031768 | ||||||
| chr19:11031949
|
C | T | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3546+1056C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11031949 | ||||||
| chr19:11032020
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0133 | 2 | HG01981.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3546+1127G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032020 | ||||||
| chr19:11032075
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3546+1182G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032075 | ||||||
| chr19:11032093
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3547-1197G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032093 | ||||||
| chr19:11032119
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3547-1171C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032119 | ||||||
| chr19:11032163
|
C | T | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3547-1127C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032163 | ||||||
| chr19:11032202
|
C | T | 1 | a0001c0002t0001g0240 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3547-1088C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032202 | ||||||
| chr19:11032447
|
A | G | 1 | a0001c0005t0001g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3547-843A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032447 | ||||||
| chr19:11032572
|
A | G | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3547-718A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032572 | ||||||
| chr19:11032666
|
C | CA | 80 | a0001c0001t0001g0053a0001c0001t0001g0075a0001c0001t0001g0147others(77): Show | 80 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.3547-609dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr19 | 11032666 | |||||
| chr19:11032666
|
CA | C | 6 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG03491.hp2 NA18941.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.3547-609delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr19 | 11032666 | |||||
| chr19:11032777
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3547-513G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032777 | ||||||
| chr19:11032945
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3547-345A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032945 | ||||||
| chr19:11032959
|
C | T | 2 | a0001c0004t0001g0121a0001c0004t0001g0160 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3547-331C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032959 | ||||||
| chr19:11032960
|
G | A | 11 | a0001c0002t0001g0080a0001c0002t0001g0232a0001c0002t0001g0239others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.3547-330G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032960 | ||||||
| chr19:11032986
|
G | A | 16 | a0001c0004t0001g0005a0001c0005t0001g0078a0001c0005t0001g0243others(13): Show | 16 | HG01255.hp1 HG01516.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.3547-304G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032986 | ||||||
| chr19:11033011
|
C | T | 19 | a0001c0002t0001g0080a0001c0002t0001g0207a0001c0002t0001g0232others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.3547-279C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11033011 | ||||||
| chr19:11033135
|
C | G | 76 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(73): Show | 76 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.3547-155C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11033135 | ||||||
| chr19:11033279
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3547-11T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11033279 | ||||||
| chr19:11033691
|
G | T | 1 | a0001c0001t0001g0162 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3775-76G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 26/34 | chr19 | 11033691 | ||||||
| chr19:11034018
|
C | T | 1 | a0001c0003t0001g0253 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3874-105C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 27/34 | chr19 | 11034018 | ||||||
| chr19:11034067
|
G | A | 1 | a0001c0003t0001g0203 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3874-56G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 27/34 | chr19 | 11034067 | ||||||
| chr19:11034284
|
G | A | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3951+84G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 28/34 | chr19 | 11034284 | ||||||
| chr19:11034411
|
C | T | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3951+211C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 28/34 | chr19 | 11034411 | ||||||
| chr19:11034449
|
G | T | 1 | a0001c0001t0001g0285 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3951+249G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 28/34 | chr19 | 11034449 | ||||||
| chr19:11034582
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3952-332A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 28/34 | chr19 | 11034582 | ||||||
| chr19:11034639
|
G | A | 1 | a0001c0001t0004g0282 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3952-275G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 28/34 | chr19 | 11034639 | ||||||
| chr19:11035148
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4170+16G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035148 | ||||||
| chr19:11035165
|
G | A | 1 | a0001c0006t0001g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4170+33G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035165 | ||||||
| chr19:11035177
|
G | A | 11 | a0001c0001t0001g0081a0001c0007t0001g0017a0001c0007t0001g0018others(8): Show | 11 | HG01071.hp1 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.4170+45G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035177 | ||||||
| chr19:11035276
|
A | T | 1 | a0001c0001t0001g0127 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4170+144A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035276 | ||||||
| chr19:11035286
|
T | C | 3 | a0001c0006t0001g0267a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG02809.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4170+154T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035286 | ||||||
| chr19:11035390
|
T | C | 2 | a0001c0001t0001g0026a0001c0024t0001g0012 | 2 | HG01109.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.4170+258T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035390 | ||||||
| chr19:11035430
|
T | C | 3 | a0001c0011t0001g0276a0001c0011t0001g0277a0001c0011t0001g0278 | 3 | HG02698.hp1 HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.4170+298T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035430 | ||||||
| chr19:11035569
|
C | G | 2 | a0001c0002t0001g0208a0001c0028t0001g0007 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4170+437C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035569 | ||||||
| chr19:11035569
|
C | T | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4170+437C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035569 | ||||||
| chr19:11035571
|
C | A | 1 | a0001c0002t0001g0146 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4170+439C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035571 | ||||||
| chr19:11035662
|
T | C | 153 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(150): Show | 153 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.4170+530T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035662 | ||||||
| chr19:11035823
|
T | C | 215 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(212): Show | 215 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(212): Show |
intron_variant | MODIFIER | c.4170+691T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035823 | ||||||
| chr19:11036108
|
C | T | 1 | a0001c0021t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4170+976C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036108 | ||||||
| chr19:11036182
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4170+1050G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036182 | ||||||
| chr19:11036379
|
C | T | 1 | a0001c0001t0004g0282 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.4170+1247C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036379 | ||||||
| chr19:11036505
|
C | T | 1 | a0001c0032t0001g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4170+1373C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036505 | ||||||
| chr19:11036534
|
C | T | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4170+1402C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036534 | ||||||
| chr19:11036566
|
G | T | 1 | a0001c0002t0001g0251 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4170+1434G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036566 | ||||||
| chr19:11036625
|
A | C | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4170+1493A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036625 | ||||||
| chr19:11036653
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4170+1521C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036653 | ||||||
| chr19:11036678
|
G | A | 4 | a0001c0001t0001g0108a0001c0001t0001g0119a0001c0001t0001g0156others(1): Show | 4 | HG00621.hp2 NA18954.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.4170+1546G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036678 | ||||||
| chr19:11036850
|
T | C | 1 | a0001c0027t0001g0014 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4170+1718T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036850 | ||||||
| chr19:11036936
|
C | T | 46 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(43): Show | 46 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.4170+1804C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036936 | ||||||
| chr19:11036939
|
G | A | 153 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(150): Show | 153 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.4170+1807G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036939 | ||||||
| chr19:11037018
|
T | G | 158 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(155): Show | 158 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.4170+1886T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037018 | ||||||
| chr19:11037120
|
G | A | 1 | a0001c0005t0001g0262 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4170+1988G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037120 | ||||||
| chr19:11037211
|
A | G | 2 | a0001c0011t0001g0276a0001c0021t0001g0175 | 2 | HG02698.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4170+2079A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037211 | ||||||
| chr19:11037408
|
A | G | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4170+2276A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037408 | ||||||
| chr19:11037437
|
C | G | 152 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(149): Show | 152 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.4170+2305C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037437 | ||||||
| chr19:11037612
|
C | T | 2 | a0001c0003t0001g0006a0001c0031t0001g0008 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4170+2480C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037612 | ||||||
| chr19:11037909
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4170+2777T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037909 | ||||||
| chr19:11038009
|
C | T | 1 | a0002c0013t0001g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4170+2877C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038009 | ||||||
| chr19:11038061
|
C | T | 12 | a0001c0002t0001g0080a0001c0002t0001g0146a0001c0002t0001g0232others(9): Show | 12 | HG00544.hp2 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.4170+2929C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038061 | ||||||
| chr19:11038093
|
A | G | 1 | a0001c0004t0001g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4170+2961A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038093 | ||||||
| chr19:11038105
|
T | C | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4170+2973T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038105 | ||||||
| chr19:11038147
|
C | T | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4170+3015C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038147 | ||||||
| chr19:11038258
|
C | G | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4171-3049C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038258 | ||||||
| chr19:11038272
|
A | G | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4171-3035A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038272 | ||||||
| chr19:11038453
|
G | A | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.4171-2854G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038453 | ||||||
| chr19:11038473
|
T | G | 1 | a0001c0003t0001g0217 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4171-2834T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038473 | ||||||
| chr19:11038555
|
A | C | 3 | a0001c0002t0001g0263a0001c0016t0001g0228a0001c0016t0001g0230 | 3 | HG02965.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4171-2752A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038555 | ||||||
| chr19:11038626
|
G | C | 1 | a0001c0001t0001g0060 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4171-2681G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038626 | ||||||
| chr19:11038698
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0179 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4171-2609G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038698 | ||||||
| chr19:11038924
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4171-2383A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038924 | ||||||
| chr19:11039309
|
G | A | 1 | a0001c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4171-1998G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039309 | ||||||
| chr19:11039325
|
G | T | 3 | a0001c0011t0001g0276a0001c0011t0001g0277a0001c0011t0001g0278 | 3 | HG02698.hp1 HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.4171-1982G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039325 | ||||||
| chr19:11039337
|
G | C | 7 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0126others(4): Show | 7 | HG01975.hp2 HG03490.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.4171-1970G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039337 | ||||||
| chr19:11039546
|
C | G | 1 | a0001c0001t0001g0108 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4171-1761C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039546 | ||||||
| chr19:11039711
|
G | A | 2 | a0001c0012t0001g0013a0001c0012t0001g0015 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4171-1596G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039711 | ||||||
| chr19:11039834
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0149 | 2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4171-1473G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039834 | ||||||
| chr19:11039865
|
G | A | 1 | a0001c0004t0001g0082 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4171-1442G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039865 | ||||||
| chr19:11039885
|
A | G | 1 | a0001c0003t0001g0148 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4171-1422A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039885 | ||||||
| chr19:11039888
|
C | G | 1 | a0001c0004t0001g0121 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4171-1419C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039888 | ||||||
| chr19:11040223
|
C | T | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4171-1084C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040223 | ||||||
| chr19:11040251
|
G | A | 2 | a0001c0002t0001g0080a0001c0002t0001g0239 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4171-1056G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040251 | ||||||
| chr19:11040323
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.4171-984G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040323 | ||||||
| chr19:11040383
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0176a0001c0027t0001g0014 | 3 | HG01099.hp1 HG03669.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.4171-924A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040383 | ||||||
| chr19:11040449
|
A | G | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.4171-858A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040449 | ||||||
| chr19:11040591
|
C | CA | 11 | a0001c0001t0001g0024a0001c0001t0001g0091a0001c0001t0001g0107others(8): Show | 11 | HG00099.hp2 HG01081.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.4171-697dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr19 | 11040591 | |||||
| chr19:11040591
|
CA | C | 101 | a0001c0001t0001g0087a0001c0001t0001g0135a0001c0002t0001g0034others(98): Show | 101 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.4171-697delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr19 | 11040591 | |||||
| chr19:11040591
|
CAA | C | 45 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.4171-698_4171-697d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr19 | 11040591 | |||||
| chr19:11040654
|
T | C | 151 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(148): Show | 151 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.4171-653T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040654 | ||||||
| chr19:11040788
|
C | T | 1 | a0001c0003t0001g0215 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.4171-519C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040788 | ||||||
| chr19:11040916
|
C | T | 1 | a0001c0002t0001g0247 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4171-391C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040916 | ||||||
| chr19:11040977
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4171-330A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040977 | ||||||
| chr19:11041010
|
C | T | 11 | a0001c0002t0001g0080a0001c0002t0001g0232a0001c0002t0001g0239others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.4171-297C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11041010 | ||||||
| chr19:11041206
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4171-101G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11041206 | ||||||
| chr19:11041216
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4171-91G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11041216 | ||||||
| chr19:11041681
|
C | T | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4424+121C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11041681 | ||||||
| chr19:11041718
|
A | G | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4424+158A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11041718 | ||||||
| chr19:11041974
|
C | T | 44 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(41): Show | 44 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.4424+414C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11041974 | ||||||
| chr19:11042119
|
G | C | 11 | a0001c0002t0001g0080a0001c0002t0001g0232a0001c0002t0001g0239others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.4424+559G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042119 | ||||||
| chr19:11042158
|
A | G | 2 | a0001c0002t0001g0208a0001c0028t0001g0007 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4424+598A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042158 | ||||||
| chr19:11042162
|
C | G | 1 | a0001c0015t0001g0021 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4424+602C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042162 | ||||||
| chr19:11042212
|
G | A | 5 | a0001c0002t0001g0257a0001c0003t0001g0206a0001c0014t0001g0233others(2): Show | 5 | HG00639.hp2 HG01261.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.4424+652G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042212 | ||||||
| chr19:11042271
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4424+711C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042271 | ||||||
| chr19:11042423
|
G | A | 1 | a0001c0003t0001g0250 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4424+863G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042423 | ||||||
| chr19:11042700
|
C | T | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4424+1140C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042700 | ||||||
| chr19:11042779
|
G | A | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4424+1219G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042779 | ||||||
| chr19:11042867
|
T | C | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4424+1307T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042867 | ||||||
| chr19:11042898
|
C | T | 10 | a0001c0007t0001g0017a0001c0007t0001g0018a0001c0007t0001g0020others(7): Show | 10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4424+1338C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042898 | ||||||
| chr19:11043144
|
C | A | 150 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(147): Show | 150 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.4424+1584C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11043144 | ||||||
| chr19:11043523
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4424+1963A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11043523 | ||||||
| chr19:11043655
|
T | TA | 8 | a0001c0002t0001g0034a0001c0002t0001g0045a0001c0002t0001g0057others(5): Show | 8 | HG01069.hp2 HG01099.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.4424+2102dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11043655 | |||||
| chr19:11043674
|
C | T | 3 | a0001c0010t0001g0009a0001c0010t0001g0010a0001c0010t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.4424+2114C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11043674 | ||||||
| chr19:11043776
|
C | T | 74 | a0001c0001t0001g0190a0001c0002t0001g0034a0001c0002t0001g0045others(71): Show | 74 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.4424+2216C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11043776 | ||||||
| chr19:11043851
|
G | A | 2 | a0001c0001t0001g0026a0001c0024t0001g0012 | 2 | HG01109.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.4424+2291G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11043851 | ||||||
| chr19:11043983
|
A | C | 2 | a0001c0016t0001g0228a0001c0016t0001g0230 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.4424+2423A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11043983 | ||||||
| chr19:11044139
|
A | G | 1 | a0001c0028t0001g0007 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4424+2579A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044139 | ||||||
| chr19:11044234
|
CTG | C | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4424+2677_4424+267 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11044234 | |||||
| chr19:11044304
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4424+2744A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044304 | ||||||
| chr19:11044308
|
A | G | 1 | a0001c0028t0001g0007 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4424+2748A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044308 | ||||||
| chr19:11044451
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4424+2891C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044451 | ||||||
| chr19:11044608
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4424+3048C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044608 | ||||||
| chr19:11044619
|
G | A | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4424+3059G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044619 | ||||||
| chr19:11044732
|
G | A | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0284 | 3 | NA18944.hp2 NA18980.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.4424+3172G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044732 | ||||||
| chr19:11044796
|
A | T | 1 | a0001c0003t0001g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4424+3236A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044796 | ||||||
| chr19:11044883
|
A | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0265 | 2 | NA18954.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.4424+3323A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044883 | ||||||
| chr19:11045059
|
G | A | 45 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.4424+3499G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11045059 | ||||||
| chr19:11045176
|
C | T | 1 | a0001c0003t0001g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4424+3616C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11045176 | ||||||
| chr19:11045318
|
T | TA | 8 | a0001c0001t0001g0086a0001c0001t0001g0142a0001c0001t0001g0143others(5): Show | 8 | HG01192.hp2 HG01515.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.4424+3769dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11045318 | |||||
| chr19:11045642
|
CT | C | 7 | a0001c0001t0001g0087a0001c0001t0001g0098a0001c0001t0001g0110others(4): Show | 7 | HG02896.hp1 HG02922.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.4424+4096delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11045642 | |||||
| chr19:11045668
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4424+4108C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11045668 | ||||||
| chr19:11045875
|
G | A | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4424+4315G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11045875 | ||||||
| chr19:11046132
|
A | C | 3 | a0001c0011t0001g0276a0001c0011t0001g0277a0001c0011t0001g0278 | 3 | HG02698.hp1 HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.4424+4572A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046132 | ||||||
| chr19:11046191
|
C | T | 6 | a0001c0002t0001g0207a0001c0009t0001g0001a0001c0009t0001g0002others(3): Show | 6 | HG02559.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4424+4631C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046191 | ||||||
| chr19:11046209
|
C | T | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4424+4649C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046209 | ||||||
| chr19:11046222
|
C | CA | 23 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0065others(20): Show | 23 | HG00408.hp2 HG00639.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.4424+4678dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11046222 | |||||
| chr19:11046385
|
G | A | 11 | a0001c0002t0001g0080a0001c0002t0001g0232a0001c0002t0001g0239others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.4424+4825G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046385 | ||||||
| chr19:11046506
|
C | T | 1 | a0001c0030t0001g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4424+4946C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046506 | ||||||
| chr19:11046592
|
C | A | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4424+5032C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046592 | ||||||
| chr19:11046681
|
G | A | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4424+5121G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046681 | ||||||
| chr19:11046747
|
A | G | 78 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(75): Show | 78 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.4424+5187A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046747 | ||||||
| chr19:11046886
|
C | T | 4 | a0001c0004t0001g0138a0001c0004t0001g0139a0001c0004t0001g0140others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4424+5326C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046886 | ||||||
| chr19:11046948
|
C | CA | 14 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0101others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.4424+5407dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11046948 | |||||
| chr19:11046948
|
C | CAA | 51 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0044others(48): Show | 51 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.4424+5406_4424+540 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11046948 | |||||
| chr19:11046948
|
C | CAAA | 17 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0051others(14): Show | 17 | HG01255.hp1 HG01516.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.4424+5405_4424+540 others(7): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11046948 | |||||
| chr19:11046948
|
CA | C | 77 | a0001c0001t0001g0028a0001c0001t0001g0123a0001c0001t0001g0161others(74): Show | 77 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.4424+5407delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11046948 | |||||
| chr19:11046983
|
C | T | 2 | a0001c0002t0001g0273a0001c0032t0001g0231 | 2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.4424+5423C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046983 | ||||||
| chr19:11047049
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4424+5489C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047049 | ||||||
| chr19:11047179
|
G | A | 2 | a0001c0008t0001g0269a0001c0008t0001g0270 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4424+5619G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047179 | ||||||
| chr19:11047190
|
T | C | 3 | a0001c0011t0001g0277a0001c0011t0001g0278a0001c0032t0001g0231 | 3 | HG02738.hp2 HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.4424+5630T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047190 | ||||||
| chr19:11047226
|
A | G | 1 | a0001c0003t0001g0224 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4424+5666A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047226 | ||||||
| chr19:11047243
|
A | G | 29 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0087others(26): Show | 29 | HG01255.hp2 HG01358.hp1 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.4424+5683A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047243 | ||||||
| chr19:11047259
|
G | T | 10 | a0001c0001t0001g0029a0001c0001t0001g0106a0001c0001t0001g0112others(7): Show | 10 | HG02257.hp1 HG02970.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.4424+5699G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047259 | ||||||
| chr19:11047342
|
A | G | 3 | a0001c0001t0001g0166a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4424+5782A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047342 | ||||||
| chr19:11047355
|
T | C | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4424+5795T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047355 | ||||||
| chr19:11047358
|
C | T | 14 | a0001c0001t0001g0076a0001c0001t0001g0168a0001c0001t0001g0171others(11): Show | 14 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.4424+5798C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047358 | ||||||
| chr19:11047371
|
A | T | 174 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.4424+5811A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047371 | ||||||
| chr19:11047379
|
C | T | 283 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.4424+5819C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047379 | ||||||
| chr19:11047410
|
G | GT | 60 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0054others(57): Show | 60 | HG00408.hp2 HG01175.hp2 HG01255.hp1 others(57): Show |
intron_variant | MODIFIER | c.4424+5865dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11047410 | |||||
| chr19:11047410
|
G | GTT | 7 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0002t0001g0146others(4): Show | 7 | HG00544.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.4424+5864_4424+586 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11047410 | |||||
| chr19:11047410
|
GTT | G | 114 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(111): Show | 114 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.4424+5864_4424+586 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11047410 | |||||
| chr19:11047473
|
A | G | 1 | a0001c0003t0001g0154 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4424+5913A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047473 | ||||||
| chr19:11047583
|
AT | A | 4 | a0001c0001t0001g0106a0001c0001t0001g0170a0001c0002t0001g0208others(1): Show | 4 | HG02970.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.4424+6029delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11047583 | |||||
| chr19:11047656
|
C | T | 1 | a0001c0011t0001g0276 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4424+6096C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047656 | ||||||
| chr19:11047657
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4424+6097G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047657 | ||||||
| chr19:11047958
|
T | A | 1 | a0001c0005t0001g0262 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4424+6398T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047958 | ||||||
| chr19:11047958
|
TTTA | T | 3 | a0001c0001t0001g0190a0001c0007t0001g0020a0001c0007t0001g0022 | 3 | HG02071.hp2 HG02080.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.4424+6413_4424+641 others(7): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11047958 | |||||
| chr19:11048046
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4424+6486C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048046 | ||||||
| chr19:11048230
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0115others(1): Show | 4 | NA18971.hp2 NA19005.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.4424+6670T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048230 | ||||||
| chr19:11048319
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4424+6759C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048319 | ||||||
| chr19:11048400
|
G | A | 70 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0051others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.4424+6840G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048400 | ||||||
| chr19:11048409
|
G | T | 2 | a0001c0003t0001g0204a0001c0003t0001g0214 | 2 | HG02080.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.4424+6849G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048409 | ||||||
| chr19:11048420
|
G | T | 38 | a0001c0002t0001g0242a0001c0002t0001g0248a0001c0003t0001g0131others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4424+6860G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048420 | ||||||
| chr19:11048554
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0106a0001c0001t0001g0170others(1): Show | 4 | HG02922.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4424+6994G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048554 | ||||||
| chr19:11048773
|
C | T | 24 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(21): Show | 24 | HG01175.hp2 HG01255.hp1 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.4424+7213C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048773 | ||||||
| chr19:11048849
|
G | T | 39 | a0001c0001t0001g0164a0001c0002t0001g0242a0001c0002t0001g0248others(36): Show | 39 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.4424+7289G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048849 | ||||||
| chr19:11049033
|
G | T | 2 | a0001c0008t0001g0269a0001c0008t0001g0270 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4424+7473G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049033 | ||||||
| chr19:11049167
|
G | A | 1 | a0001c0002t0001g0221 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4424+7607G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049167 | ||||||
| chr19:11049213
|
T | C | 40 | a0001c0001t0001g0164a0001c0002t0001g0242a0001c0002t0001g0248others(37): Show | 40 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.4424+7653T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049213 | ||||||
| chr19:11049226
|
C | T | 6 | a0001c0008t0001g0269a0001c0008t0001g0270a0001c0011t0001g0276others(3): Show | 6 | HG02280.hp2 HG02698.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.4424+7666C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049226 | ||||||
| chr19:11049340
|
G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4424+7780G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049340 | ||||||
| chr19:11049429
|
G | T | 1 | a0001c0002t0001g0232 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4424+7869G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049429 | ||||||
| chr19:11049485
|
G | GT | 6 | a0001c0001t0001g0122a0001c0001t0001g0142a0001c0001t0001g0145others(3): Show | 6 | HG01192.hp2 HG02109.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4424+7942dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11049485 | |||||
| chr19:11049485
|
G | T | 26 | a0001c0001t0001g0044a0001c0001t0001g0063a0001c0001t0001g0109others(23): Show | 26 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.4424+7925G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049485 | ||||||
| chr19:11049485
|
GT | G | 44 | a0001c0001t0001g0164a0001c0001t0001g0173a0001c0002t0001g0242others(41): Show | 44 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.4424+7942delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11049485 | |||||
| chr19:11049492
|
T | G | 1 | a0001c0004t0001g0072 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.4424+7932T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049492 | ||||||
| chr19:11049493
|
T | G | 41 | a0001c0001t0001g0164a0001c0002t0001g0242a0001c0002t0001g0248others(38): Show | 41 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.4424+7933T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049493 | ||||||
| chr19:11049502
|
T | G | 2 | a0001c0016t0001g0228a0001c0031t0001g0008 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4424+7942T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049502 | ||||||
| chr19:11049789
|
G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4424+8229G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049789 | ||||||
| chr19:11049856
|
C | G | 1 | a0001c0001t0001g0097 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4424+8296C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049856 | ||||||
| chr19:11049932
|
G | A | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4425-8323G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049932 | ||||||
| chr19:11049953
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0170 | 2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4425-8302T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049953 | ||||||
| chr19:11050110
|
G | C | 2 | a0001c0008t0001g0269a0001c0008t0001g0270 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4425-8145G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050110 | ||||||
| chr19:11050167
|
G | A | 2 | a0001c0001t0001g0177a0001c0002t0001g0236 | 2 | HG02040.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.4425-8088G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050167 | ||||||
| chr19:11050252
|
G | T | 1 | a0001c0004t0001g0082 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4425-8003G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050252 | ||||||
| chr19:11050283
|
C | T | 1 | a0001c0002t0001g0242 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4425-7972C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050283 | ||||||
| chr19:11050708
|
A | G | 1 | a0001c0002t0001g0279 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4425-7547A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050708 | ||||||
| chr19:11050851
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4425-7404A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050851 | ||||||
| chr19:11050861
|
C | A | 38 | a0001c0002t0001g0242a0001c0002t0001g0248a0001c0003t0001g0131others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4425-7394C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050861 | ||||||
| chr19:11050869
|
T | C | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4425-7386T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050869 | ||||||
| chr19:11051201
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4425-7054C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051201 | ||||||
| chr19:11051309
|
A | G | 2 | a0001c0010t0001g0009a0001c0010t0001g0010 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.4425-6946A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051309 | ||||||
| chr19:11051322
|
G | A | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4425-6933G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051322 | ||||||
| chr19:11051368
|
G | A | 1 | a0001c0002t0001g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4425-6887G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051368 | ||||||
| chr19:11051415
|
C | G | 1 | a0001c0019t0001g0192 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4425-6840C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051415 | ||||||
| chr19:11051465
|
G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-6790G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051465 | ||||||
| chr19:11051491
|
C | CT | 22 | a0001c0001t0001g0051a0001c0001t0001g0141a0001c0001t0001g0168others(19): Show | 22 | HG00544.hp2 HG01069.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.4425-6746dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11051491 | |||||
| chr19:11051491
|
C | CTT | 8 | a0001c0003t0001g0203a0001c0004t0001g0025a0001c0004t0001g0082others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4425-6747_4425-674 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11051491 | |||||
| chr19:11051491
|
CT | C | 9 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0001g0110others(6): Show | 9 | HG01168.hp1 HG02280.hp2 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.4425-6746delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11051491 | |||||
| chr19:11051522
|
C | T | 2 | a0001c0008t0001g0269a0001c0008t0001g0270 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4425-6733C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051522 | ||||||
| chr19:11051547
|
G | T | 1 | a0001c0014t0001g0235 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4425-6708G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051547 | ||||||
| chr19:11051615
|
C | T | 4 | a0001c0011t0001g0276a0001c0011t0001g0277a0001c0011t0001g0278others(1): Show | 4 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.4425-6640C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051615 | ||||||
| chr19:11051660
|
T | C | 1 | a0001c0002t0001g0273 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4425-6595T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051660 | ||||||
| chr19:11051699
|
T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0275 | 2 | HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.4425-6556T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051699 | ||||||
| chr19:11052203
|
T | C | 1 | a0001c0007t0001g0022 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4425-6052T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052203 | ||||||
| chr19:11052367
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4425-5888G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052367 | ||||||
| chr19:11052585
|
A | C | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-5670A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052585 | ||||||
| chr19:11052590
|
C | T | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4425-5665C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052590 | ||||||
| chr19:11052715
|
G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-5540G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052715 | ||||||
| chr19:11052720
|
C | T | 2 | a0001c0018t0001g0039a0001c0018t0001g0157 | 2 | NA18940.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.4425-5535C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052720 | ||||||
| chr19:11052736
|
C | G | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4425-5519C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052736 | ||||||
| chr19:11052886
|
C | T | 195 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0035others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.4425-5369C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052886 | ||||||
| chr19:11052925
|
G | T | 38 | a0001c0002t0001g0242a0001c0002t0001g0248a0001c0003t0001g0131others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4425-5330G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052925 | ||||||
| chr19:11053013
|
A | G | 8 | a0001c0003t0001g0137a0001c0003t0001g0210a0001c0003t0001g0218others(5): Show | 8 | HG01074.hp2 HG01168.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.4425-5242A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053013 | ||||||
| chr19:11053119
|
G | C | 5 | a0001c0001t0001g0036a0001c0001t0001g0106a0001c0001t0001g0170others(2): Show | 5 | HG02922.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4425-5136G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053119 | ||||||
| chr19:11053138
|
C | T | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4425-5117C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053138 | ||||||
| chr19:11053148
|
T | C | 68 | a0001c0002t0001g0208a0001c0002t0001g0242a0001c0002t0001g0248others(65): Show | 68 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.4425-5107T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053148 | ||||||
| chr19:11053171
|
C | T | 102 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(99): Show | 102 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(99): Show |
intron_variant | MODIFIER | c.4425-5084C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053171 | ||||||
| chr19:11053221
|
T | C | 196 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.4425-5034T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053221 | ||||||
| chr19:11053292
|
T | C | 5 | a0001c0004t0001g0138a0001c0004t0001g0139a0001c0004t0001g0140others(2): Show | 5 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4425-4963T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053292 | ||||||
| chr19:11053372
|
T | A | 1 | a0001c0002t0001g0236 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.4425-4883T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053372 | ||||||
| chr19:11053379
|
G | A | 4 | a0001c0011t0001g0276a0001c0011t0001g0277a0001c0011t0001g0278others(1): Show | 4 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.4425-4876G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053379 | ||||||
| chr19:11053391
|
T | G | 195 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0035others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.4425-4864T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053391 | ||||||
| chr19:11053451
|
C | CA | 25 | a0001c0001t0001g0101a0001c0001t0001g0106a0001c0001t0001g0110others(22): Show | 25 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.4425-4787dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11053451 | |||||
| chr19:11053468
|
AG | A | 8 | a0001c0001t0001g0063a0001c0001t0001g0090a0001c0002t0001g0220others(5): Show | 8 | HG01257.hp2 HG03195.hp2 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.4425-4786delG | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053468 | ||||||
| chr19:11053469
|
G | A | 188 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0035others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.4425-4786G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053469 | ||||||
| chr19:11053768
|
A | G | 1 | a0001c0002t0001g0251 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4425-4487A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053768 | ||||||
| chr19:11053784
|
G | A | 38 | a0001c0002t0001g0242a0001c0002t0001g0248a0001c0003t0001g0131others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4425-4471G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053784 | ||||||
| chr19:11053830
|
G | T | 2 | a0001c0004t0001g0025a0001c0004t0001g0167 | 2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4425-4425G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053830 | ||||||
| chr19:11053867
|
C | T | 1 | a0001c0002t0001g0249 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4425-4388C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053867 | ||||||
| chr19:11053892
|
C | A | 67 | a0001c0002t0001g0242a0001c0002t0001g0248a0001c0003t0001g0006others(64): Show | 67 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.4425-4363C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053892 | ||||||
| chr19:11053897
|
C | G | 1 | a0001c0001t0001g0162 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.4425-4358C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053897 | ||||||
| chr19:11053991
|
G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-4264G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053991 | ||||||
| chr19:11054021
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0166a0001c0001t0001g0186 | 3 | HG01952.hp1 HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4425-4234C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054021 | ||||||
| chr19:11054086
|
G | A | 2 | a0001c0010t0001g0009a0001c0010t0001g0010 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.4425-4169G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054086 | ||||||
| chr19:11054105
|
A | G | 69 | a0001c0002t0001g0208a0001c0002t0001g0242a0001c0002t0001g0248others(66): Show | 69 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.4425-4150A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054105 | ||||||
| chr19:11054114
|
A | G | 29 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0003t0001g0203others(26): Show | 29 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4425-4141A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054114 | ||||||
| chr19:11054292
|
C | G | 1 | a0001c0001t0001g0194 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4425-3963C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054292 | ||||||
| chr19:11054292
|
C | T | 123 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0035others(120): Show | 123 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.4425-3963C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054292 | ||||||
| chr19:11054376
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.4425-3879A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054376 | ||||||
| chr19:11054477
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4425-3778C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054477 | ||||||
| chr19:11054604
|
C | G | 4 | a0001c0001t0001g0098a0001c0001t0001g0103a0001c0001t0001g0105others(1): Show | 4 | NA18747.hp1 NA18948.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.4425-3651C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054604 | ||||||
| chr19:11054634
|
A | G | 1 | a0001c0002t0001g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4425-3621A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054634 | ||||||
| chr19:11054746
|
G | A | 1 | a0001c0007t0001g0020 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4425-3509G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054746 | ||||||
| chr19:11054943
|
G | A | 29 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0003t0001g0203others(26): Show | 29 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4425-3312G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054943 | ||||||
| chr19:11054978
|
C | T | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-3277C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054978 | ||||||
| chr19:11055090
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4425-3165C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055090 | ||||||
| chr19:11055301
|
T | C | 1 | a0001c0002t0001g0232 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4425-2954T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055301 | ||||||
| chr19:11055315
|
G | C | 1 | a0001c0001t0001g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4425-2940G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055315 | ||||||
| chr19:11055340
|
T | C | 105 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(102): Show | 105 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.4425-2915T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055340 | ||||||
| chr19:11055380
|
G | T | 1 | a0001c0003t0001g0203 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4425-2875G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055380 | ||||||
| chr19:11055384
|
A | G | 28 | a0001c0002t0001g0208a0001c0003t0001g0203a0001c0003t0001g0206others(25): Show | 28 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.4425-2871A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055384 | ||||||
| chr19:11055487
|
C | T | 34 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(31): Show | 34 | HG00544.hp2 HG01175.hp2 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.4425-2768C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055487 | ||||||
| chr19:11055495
|
G | T | 25 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0003t0001g0203others(22): Show | 25 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.4425-2760G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055495 | ||||||
| chr19:11055617
|
T | C | 101 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(98): Show | 101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.4425-2638T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055617 | ||||||
| chr19:11055755
|
CT | C | 38 | a0001c0002t0001g0242a0001c0002t0001g0248a0001c0003t0001g0131others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4425-2492delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11055755 | |||||
| chr19:11055763
|
T | C | 29 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0003t0001g0203others(26): Show | 29 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4425-2492T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055763 | ||||||
| chr19:11055800
|
T | C | 69 | a0001c0001t0001g0063a0001c0001t0001g0134a0001c0002t0001g0208others(66): Show | 69 | HG00099.hp1 HG00544.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.4425-2455T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055800 | ||||||
| chr19:11056115
|
A | G | 25 | a0001c0001t0001g0063a0001c0001t0001g0109a0001c0001t0001g0110others(22): Show | 25 | HG00544.hp1 HG00558.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.4425-2140A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056115 | ||||||
| chr19:11056151
|
G | A | 53 | a0001c0002t0001g0242a0001c0002t0001g0248a0001c0003t0001g0131others(50): Show | 53 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.4425-2104G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056151 | ||||||
| chr19:11056203
|
G | A | 5 | a0001c0001t0001g0036a0001c0001t0001g0106a0001c0001t0001g0170others(2): Show | 5 | HG02922.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4425-2052G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056203 | ||||||
| chr19:11056317
|
G | A | 1 | a0001c0015t0001g0023 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4425-1938G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056317 | ||||||
| chr19:11056333
|
A | C | 5 | a0001c0005t0001g0078a0001c0005t0001g0243a0001c0005t0001g0244others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.4425-1922A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056333 | ||||||
| chr19:11056395
|
A | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0106a0001c0001t0001g0170others(2): Show | 5 | HG02922.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4425-1860A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056395 | ||||||
| chr19:11056437
|
C | T | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0161 | 3 | HG02257.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.4425-1818C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056437 | ||||||
| chr19:11056543
|
C | T | 38 | a0001c0002t0001g0242a0001c0002t0001g0248a0001c0003t0001g0131others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4425-1712C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056543 | ||||||
| chr19:11056764
|
C | G | 35 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(32): Show | 35 | HG00544.hp2 HG01175.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.4425-1491C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056764 | ||||||
| chr19:11056819
|
A | G | 29 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0003t0001g0203others(26): Show | 29 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4425-1436A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056819 | ||||||
| chr19:11056867
|
C | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0047 | 2 | HG00597.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.4425-1388C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056867 | ||||||
| chr19:11056905
|
G | A | 23 | a0001c0003t0001g0006a0001c0003t0001g0203a0001c0003t0001g0206others(20): Show | 23 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.4425-1350G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056905 | ||||||
| chr19:11056936
|
A | C | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-1319A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056936 | ||||||
| chr19:11056953
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4425-1302G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056953 | ||||||
| chr19:11056964
|
C | T | 29 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0003t0001g0203others(26): Show | 29 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4425-1291C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056964 | ||||||
| chr19:11056989
|
C | T | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4425-1266C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056989 | ||||||
| chr19:11057043
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4425-1212A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057043 | ||||||
| chr19:11057104
|
T | C | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4425-1151T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057104 | ||||||
| chr19:11057146
|
C | T | 1 | a0001c0002t0001g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4425-1109C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057146 | ||||||
| chr19:11057284
|
G | C | 285 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.4425-971G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057284 | ||||||
| chr19:11057324
|
G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-931G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057324 | ||||||
| chr19:11057330
|
G | C | 1 | a0001c0003t0001g0252 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4425-925G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057330 | ||||||
| chr19:11057353
|
T | C | 67 | a0001c0002t0001g0208a0001c0002t0001g0242a0001c0002t0001g0248others(64): Show | 67 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.4425-902T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057353 | ||||||
| chr19:11057362
|
A | G | 38 | a0001c0002t0001g0242a0001c0002t0001g0248a0001c0003t0001g0131others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4425-893A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057362 | ||||||
| chr19:11057379
|
G | A | 2 | a0001c0008t0001g0269a0001c0008t0001g0270 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4425-876G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057379 | ||||||
| chr19:11057453
|
G | A | 1 | a0001c0015t0001g0023 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4425-802G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057453 | ||||||
| chr19:11057539
|
A | T | 1 | a0001c0001t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4425-716A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057539 | ||||||
| chr19:11057585
|
C | T | 42 | a0001c0002t0001g0242a0001c0002t0001g0248a0001c0003t0001g0006others(39): Show | 42 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.4425-670C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057585 | ||||||
| chr19:11057619
|
C | T | 1 | a0001c0002t0001g0226 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4425-636C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057619 | ||||||
| chr19:11057626
|
G | C | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-629G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057626 | ||||||
| chr19:11057874
|
G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-381G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057874 | ||||||
| chr19:11057950
|
A | G | 29 | a0001c0002t0001g0208a0001c0003t0001g0006a0001c0003t0001g0203others(26): Show | 29 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4425-305A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057950 | ||||||
| chr19:11058028
|
C | G | 3 | a0001c0004t0001g0025a0001c0004t0001g0167a0001c0028t0001g0007 | 3 | HG02257.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4425-227C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11058028 | ||||||
| chr19:11058093
|
C | T | 15 | a0001c0003t0001g0203a0001c0003t0001g0206a0001c0003t0001g0209others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.4425-162C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11058093 | ||||||
| chr19:11058106
|
C | CA | 61 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0096others(58): Show | 61 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.4425-136dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11058106 | |||||
| chr19:11058122
|
G | A | 67 | a0001c0002t0001g0208a0001c0002t0001g0242a0001c0002t0001g0248others(64): Show | 67 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.4425-133G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11058122 | ||||||
| chr19:11058185
|
C | T | 1 | a0001c0003t0001g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4425-70C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11058185 | ||||||
| chr19:11058220
|
A | G | 104 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(101): Show | 104 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(101): Show |
intron_variant | MODIFIER | c.4425-35A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11058220 | ||||||
| chr19:11058385
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4533+22C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/34 | chr19 | 11058385 | ||||||
| chr19:11058393
|
A | G | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4533+30A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/34 | chr19 | 11058393 | ||||||
| chr19:11058481
|
G | T | 3 | a0001c0011t0001g0277a0001c0011t0001g0278a0001c0032t0001g0231 | 3 | HG02738.hp2 HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.4533+118G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/34 | chr19 | 11058481 | ||||||
| chr19:11058629
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0136a0001c0001t0001g0149 | 3 | HG00735.hp2 HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4534-159T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/34 | chr19 | 11058629 | ||||||
| chr19:11058705
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0126a0001c0001t0001g0155 | 3 | HG03490.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.4534-83G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/34 | chr19 | 11058705 | ||||||
| chr19:11058705
|
G | T | 1 | a0001c0001t0001g0151 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4534-83G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/34 | chr19 | 11058705 | ||||||
| chr19:11058901
|
G | A | 3 | a0001c0004t0001g0121a0001c0004t0001g0160a0001c0008t0001g0266 | 3 | HG02145.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4635+12G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | chr19 | 11058901 | ||||||
| chr19:11059230
|
CTCTG | C | 15 | a0001c0003t0001g0217a0001c0003t0001g0223a0001c0003t0001g0246others(12): Show | 15 | HG02145.hp1 HG02280.hp2 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.4635+347_4635+350d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr19 | 11059230 | |||||
| chr19:11059271
|
T | C | 105 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(102): Show | 105 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.4635+382T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | chr19 | 11059271 | ||||||
| chr19:11059487
|
G | T | 2 | a0001c0001t0001g0158a0001c0026t0001g0281 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4636-266G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | chr19 | 11059487 | ||||||
| chr19:11059615
|
C | T | 5 | a0001c0003t0001g0006a0001c0004t0001g0025a0001c0004t0001g0167others(2): Show | 5 | HG02257.hp1 HG02622.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4636-138C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | chr19 | 11059615 | ||||||
| chr19:11059631
|
G | A | 3 | a0001c0009t0001g0001a0001c0009t0001g0002a0001c0009t0001g0003 | 3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4636-122G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | chr19 | 11059631 | ||||||
| chr19:11059633
|
A | T | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4636-120A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | chr19 | 11059633 | ||||||
| chr19:11059684
|
G | GGGGCCA | 5 | a0001c0004t0001g0121a0001c0004t0001g0160a0001c0008t0001g0266others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4636-63_4636-58dup others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr19 | 11059684 | |||||
| chr19:11059886
|
G | C | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | splice_donor_variant&intron_variant | HIGH | c.4768+1G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059886 | ||||||
| chr19:11059887
|
T | A | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | splice_donor_variant&intron_variant | HIGH | c.4768+2T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059887 | ||||||
| chr19:11059888
|
G | C | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.4768+3G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059888 | ||||||
| chr19:11059890
|
G | C | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.4768+5G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059890 | ||||||
| chr19:11059893
|
C | T | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.4768+8C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059893 | ||||||
| chr19:11059894
|
C | A | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4768+9C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059894 | ||||||
| chr19:11059895
|
G | T | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4768+10G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059895 | ||||||
| chr19:11059896
|
G | C | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4768+11G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059896 | ||||||
| chr19:11059897
|
G | A | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4768+12G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059897 | ||||||
| chr19:11059899
|
G | A | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4768+14G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059899 | ||||||
| chr19:11059900
|
G | C | 2 | a0001c0003t0001g0224a0001c0003t0001g0225 | 2 | HG01243.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.4768+15G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059900 | ||||||
| chr19:11059900
|
G | T | 1 | a0004c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4768+15G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059900 | ||||||
| chr19:11059901
|
G | T | 6 | a0001c0002t0001g0080a0001c0002t0001g0239a0001c0006t0001g0267others(3): Show | 6 | HG02451.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4768+16G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059901 | ||||||
| chr19:11059909
|
C | A | 1 | a0001c0002t0001g0255 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4768+24C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059909 | ||||||
| chr19:11059983
|
T | A | 4 | a0001c0003t0001g0006a0001c0004t0001g0025a0001c0004t0001g0167others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.4769-62T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059983 | ||||||
| chr19:11059987
|
T | G | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4769-58T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059987 | ||||||
| chr19:11060020
|
G | A | 10 | a0001c0003t0001g0217a0001c0003t0001g0223a0001c0003t0001g0246others(7): Show | 10 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.4769-25G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11060020 | ||||||
| chr19:11060239
|
C | T | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4911+52C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060239 | ||||||
| chr19:11060287
|
C | T | 10 | a0001c0003t0001g0217a0001c0003t0001g0223a0001c0003t0001g0246others(7): Show | 10 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.4911+100C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060287 | ||||||
| chr19:11060306
|
G | A | 11 | a0001c0003t0001g0217a0001c0003t0001g0223a0001c0003t0001g0246others(8): Show | 11 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.4911+119G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060306 | ||||||
| chr19:11060308
|
G | A | 11 | a0001c0003t0001g0217a0001c0003t0001g0223a0001c0003t0001g0246others(8): Show | 11 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.4911+121G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060308 | ||||||
| chr19:11060310
|
C | G | 11 | a0001c0003t0001g0217a0001c0003t0001g0223a0001c0003t0001g0246others(8): Show | 11 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.4911+123C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060310 | ||||||
| chr19:11060334
|
G | T | 10 | a0001c0003t0001g0217a0001c0003t0001g0223a0001c0003t0001g0246others(7): Show | 10 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.4911+147G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060334 | ||||||
| chr19:11060555
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.4911+368G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060555 | ||||||
| chr19:11060605
|
A | C | 62 | a0001c0003t0001g0131a0001c0003t0001g0137a0001c0003t0001g0148others(59): Show | 62 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.4911+418A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060605 | ||||||
| chr19:11060642
|
G | A | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4911+455G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060642 | ||||||
| chr19:11060663
|
T | A | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4911+476T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060663 | ||||||
| chr19:11060780
|
G | C | 5 | a0001c0004t0001g0121a0001c0004t0001g0160a0001c0008t0001g0266others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4911+593G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060780 | ||||||
| chr19:11060808
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4911+621C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060808 | ||||||
| chr19:11060924
|
T | C | 47 | a0001c0003t0001g0131a0001c0003t0001g0137a0001c0003t0001g0148others(44): Show | 47 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.4911+737T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060924 | ||||||
| chr19:11061117
|
G | A | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4912-667G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061117 | ||||||
| chr19:11061148
|
A | G | 10 | a0001c0003t0001g0217a0001c0003t0001g0223a0001c0003t0001g0246others(7): Show | 10 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.4912-636A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061148 | ||||||
| chr19:11061185
|
C | CT | 9 | a0001c0003t0001g0204a0001c0003t0001g0217a0001c0003t0001g0223others(6): Show | 9 | HG02698.hp1 HG03942.hp1 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.4912-596dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061185 | |||||
| chr19:11061188
|
T | TAAAAAAA others(3): Show |
3 | a0001c0001t0001g0027a0001c0001t0001g0113a0001c0002t0001g0263 | 3 | HG02280.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4912-588_4912-579d others(12): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061188 | |||||
| chr19:11061188
|
T | TAAAAAAA others(4): Show |
1 | a0001c0028t0001g0007 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4912-589_4912-579d others(13): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061188 | |||||
| chr19:11061188
|
T | TAAAAAAA others(5): Show |
2 | a0001c0001t0001g0112a0001c0016t0001g0230 | 2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4912-590_4912-579d others(14): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061188 | |||||
| chr19:11061188
|
T | TTA | 4 | a0001c0003t0001g0219a0001c0004t0001g0167a0001c0014t0001g0233others(1): Show | 4 | HG00099.hp1 HG01515.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.4912-596_4912-595i others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061188 | ||||||
| chr19:11061188
|
TAA | T | 29 | a0001c0001t0001g0026a0001c0001t0001g0049a0001c0001t0001g0053others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.4912-580_4912-579d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061188 | |||||
| chr19:11061188
|
TAAA | T | 6 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 6 | HG00558.hp2 HG01884.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.4912-581_4912-579d others(5): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061188 | |||||
| chr19:11061188
|
TAAAA | T | 15 | a0001c0001t0001g0086a0001c0001t0001g0097a0001c0001t0001g0098others(12): Show | 15 | HG00735.hp2 HG01192.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.4912-582_4912-579d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061188 | |||||
| chr19:11061189
|
A | T | 52 | a0001c0003t0001g0006a0001c0003t0001g0131a0001c0003t0001g0137others(49): Show | 52 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.4912-595A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061189 | ||||||
| chr19:11061196
|
AAAAAAAA others(15): Show |
A | 16 | a0001c0003t0001g0203a0001c0003t0001g0206a0001c0003t0001g0209others(13): Show | 16 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.4912-586_4912-565d others(24): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061196 | |||||
| chr19:11061198
|
AAAAAAAA others(15): Show |
A | 1 | a0001c0004t0001g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4912-584_4912-563d others(24): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061198 | |||||
| chr19:11061200
|
A | T | 3 | a0001c0001t0001g0061a0001c0003t0001g0204a0001c0014t0001g0233 | 3 | HG01515.hp2 HG04184.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.4912-584A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061200 | ||||||
| chr19:11061200
|
AAAAAAT | A | 7 | a0001c0001t0001g0129a0001c0001t0001g0158a0001c0001t0001g0162others(4): Show | 7 | HG01884.hp1 HG02083.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.4912-582_4912-577d others(8): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061200 | |||||
| chr19:11061201
|
AAAAAT | A | 6 | a0001c0001t0001g0047a0001c0001t0001g0076a0001c0001t0001g0077others(3): Show | 6 | HG00558.hp1 HG01167.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.4912-581_4912-577d others(7): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061201 | |||||
| chr19:11061202
|
A | AATATATA others(21): Show |
1 | a0001c0001t0001g0132 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4912-581_4912-580i others(30): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061202 | |||||
| chr19:11061202
|
A | T | 10 | a0001c0001t0001g0046a0001c0001t0001g0061a0001c0001t0001g0062others(7): Show | 10 | HG00099.hp1 HG01071.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.4912-582A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061202 | ||||||
| chr19:11061202
|
AAAAT | A | 49 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0038others(46): Show | 49 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.4912-580_4912-577d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061202 | |||||
| chr19:11061202
|
AAAATAT | A | 22 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0111others(19): Show | 22 | HG01192.hp1 HG01243.hp2 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.4912-580_4912-575d others(8): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061202 | |||||
| chr19:11061202
|
AAAATATA others(9): Show |
A | 1 | a0001c0001t0001g0152 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4912-580_4912-565d others(18): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061202 | |||||
| chr19:11061202
|
AAAATATA others(13): Show |
A | 1 | a0001c0001t0001g0116 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4912-580_4912-561d others(22): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061202 | |||||
| chr19:11061204
|
A | AAAAAAAA others(31): Show |
1 | a0001c0002t0001g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4912-579_4912-578i others(40): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061204
|
A | AAAAAAAA others(26): Show |
1 | a0001c0002t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4912-579_4912-578i others(35): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061204
|
A | AAAAAAAA others(3): Show |
1 | a0001c0016t0001g0228 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4912-579_4912-578i others(12): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061204
|
A | AAAAAAAA others(11): Show |
1 | a0001c0006t0001g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4912-579_4912-578i others(20): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061204
|
A | AAAAAAAA others(15): Show |
1 | a0001c0021t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4912-579_4912-578i others(24): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061204
|
A | AAAAAAAA others(13): Show |
1 | a0001c0030t0001g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4912-579_4912-578i others(22): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061204
|
A | AAAAAAAA others(23): Show |
2 | a0001c0006t0001g0271a0001c0006t0001g0272 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4912-579_4912-578i others(32): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061204
|
A | AAAAAAAT others(4): Show |
1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4912-579_4912-578i others(13): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061204
|
A | AAAAAATA others(3): Show |
1 | a0001c0001t0001g0028 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4912-579_4912-578i others(12): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061204
|
A | AAAAAATA others(7): Show |
1 | a0001c0002t0001g0146 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4912-579_4912-578i others(16): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061204
|
A | T | 35 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0046others(32): Show | 35 | HG00099.hp1 HG00544.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.4912-580A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061204 | ||||||
| chr19:11061204
|
AAT | A | 11 | a0001c0001t0001g0044a0001c0001t0001g0075a0001c0001t0001g0094others(8): Show | 11 | HG00438.hp2 HG00673.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.4912-543_4912-542d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061204
|
AATAT | A | 13 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0073others(10): Show | 13 | HG01358.hp2 HG01981.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.4912-545_4912-542d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061204
|
AATATAT | A | 16 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0109others(13): Show | 16 | HG00621.hp1 HG00673.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.4912-547_4912-542d others(8): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061204
|
AATATATA others(11): Show |
A | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4912-559_4912-542d others(20): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | |||||
| chr19:11061205
|
ATATAT | A | 6 | a0001c0002t0001g0238a0001c0007t0001g0017a0001c0007t0001g0020others(3): Show | 6 | HG01255.hp1 HG01516.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.4912-578_4912-574d others(7): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061205 | ||||||
| chr19:11061205
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4912-578_4912-562d others(19): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061205 | ||||||
| chr19:11061206
|
T | A | 20 | a0001c0001t0001g0087a0001c0001t0001g0112a0001c0001t0001g0113others(17): Show | 20 | HG02280.hp1 HG02698.hp1 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.4912-578T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061206 | ||||||
| chr19:11061208
|
T | A | 17 | a0001c0001t0001g0044a0001c0001t0001g0112a0001c0002t0001g0207others(14): Show | 17 | HG00438.hp2 HG01175.hp2 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.4912-576T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061208 | ||||||
| chr19:11061210
|
T | A | 18 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0002t0001g0207others(15): Show | 18 | HG01175.hp2 HG01981.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.4912-574T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061210 | ||||||
| chr19:11061212
|
T | A | 10 | a0001c0003t0001g0217a0001c0003t0001g0223a0001c0003t0001g0246others(7): Show | 10 | HG02622.hp1 HG02698.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.4912-572T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061212 | ||||||
| chr19:11061214
|
T | A | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4912-570T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061214 | ||||||
| chr19:11061216
|
T | A | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4912-568T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061216 | ||||||
| chr19:11061224
|
T | A | 2 | a0001c0001t0001g0179a0001c0031t0001g0008 | 2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4912-560T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061224 | ||||||
| chr19:11061226
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4912-558T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061226 | ||||||
| chr19:11061228
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4912-556T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061228 | ||||||
| chr19:11061230
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4912-554T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061230 | ||||||
| chr19:11061232
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4912-552T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061232 | ||||||
| chr19:11061276
|
C | A | 2 | a0001c0004t0001g0138a0001c0008t0001g0266 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4912-508C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061276 | ||||||
| chr19:11061328
|
T | C | 52 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(49): Show | 52 | HG00544.hp2 HG01069.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.4912-456T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061328 | ||||||
| chr19:11061331
|
G | A | 3 | a0001c0011t0001g0277a0001c0011t0001g0278a0001c0032t0001g0231 | 3 | HG02738.hp2 HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.4912-453G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061331 | ||||||
| chr19:11061445
|
G | A | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4912-339G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061445 | ||||||
| chr19:11061494
|
G | A | 1 | a0001c0022t0001g0201 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4912-290G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061494 | ||||||
| chr19:11061537
|
G | A | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4912-247G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061537 | ||||||
| chr19:11061623
|
G | A | 46 | a0001c0003t0001g0131a0001c0003t0001g0137a0001c0003t0001g0148others(43): Show | 46 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.4912-161G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061623 | ||||||
| chr19:11061646
|
G | C | 1 | a0001c0032t0001g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4912-138G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061646 | ||||||
| chr19:11061671
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4912-113C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061671 | ||||||
| chr19:11061679
|
A | G | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4912-105A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061679 | ||||||
| chr19:11061736
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4912-48C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061736 |