Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9024 |
|---|---|
| ensemblid | ENSG00000174672.16 |
| hgncid | 11405 |
| symbol | BRSK2 |
| name | BR serine/threonine kinase 2 |
| refseq_nuc | NM_001256627.2 |
| refseq_prot | NP_001243556.1 |
| ensembl_nuc | ENST00000528841.6 |
| ensembl_prot | ENSP00000432000.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 1389934 |
| end | 1462689 |
| strand | + |
| ver | v1.2 |
| region | chr11:1389934-1462689 |
| region5000 | chr11:1384934-1467689 |
| regionname0 | BRSK2_chr11_1389934_1462689 |
| regionname5000 | BRSK2_chr11_1384934_1467689 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 736 | 210 | 62 | 43 | 69 | 13 | 22 | 54 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002 | 1/0 | 736 | 145 | 30 | 28 | 64 | 3 | 19 | 45 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0003 | 0/0 | 736 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0004 | 0/0 | 736 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0005 | 0/0 | 736 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0006 | 0/0 | 736 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0007 | 0/0 | 625 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2211 | 180 | 53 | 40 | 51 | 13 | 22 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0002 | 1/0 | 2211 | 136 | 25 | 26 | 64 | 1 | 19 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0003 | 0/0 | 2211 | 20 | 7 | 1 | 12 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0004 | 0/0 | 2211 | 6 | 0 | 0 | 6 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0005 | 0/0 | 2211 | 3 | 2 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0006 | 0/0 | 2211 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0007 | 0/0 | 2211 | 2 | 0 | 0 | 0 | 2 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0008 | 0/0 | 2211 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0009 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0010 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0011 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0012 | 0/0 | 2211 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0013 | 0/0 | 2186 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0014 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0015 | 0/0 | 2211 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0016 | 0/0 | 2211 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| c0017 | 0/0 | 2211 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2319 | 79 | 20 | 13 | 36 | 1 | 8 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0002 | 0/0 | 2318 | 44 | 12 | 3 | 24 | 1 | 4 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0003 | 0/0 | 2319 | 35 | 18 | 4 | 8 | 4 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0004 | 0/0 | 2320 | 23 | 2 | 9 | 7 | 2 | 3 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0005 | 0/0 | 2318 | 21 | 2 | 7 | 9 | 0 | 3 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0006 | 0/0 | 2320 | 11 | 0 | 5 | 0 | 2 | 4 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0007 | 0/0 | 2315 | 10 | 0 | 4 | 6 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0008 | 0/0 | 2319 | 9 | 0 | 1 | 6 | 0 | 2 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0009 | 0/0 | 2319 | 8 | 0 | 0 | 8 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0010 | 0/0 | 2319 | 7 | 0 | 2 | 2 | 2 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0011 | 0/0 | 2316 | 5 | 0 | 0 | 4 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0012 | 0/0 | 2315 | 5 | 0 | 0 | 5 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0013 | 0/0 | 2319 | 4 | 4 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0014 | 0/0 | 2319 | 4 | 3 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0015 | 0/0 | 2320 | 4 | 2 | 0 | 0 | 0 | 2 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0016 | 0/0 | 2321 | 4 | 2 | 1 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0017 | 0/0 | 2316 | 3 | 0 | 0 | 3 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0018 | 0/0 | 2320 | 3 | 0 | 2 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0019 | 0/0 | 2321 | 3 | 3 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0020 | 0/0 | 2319 | 3 | 0 | 0 | 2 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0021 | 0/0 | 2320 | 3 | 0 | 2 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0022 | 0/0 | 2318 | 3 | 0 | 3 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0023 | 0/0 | 2320 | 3 | 1 | 1 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0024 | 0/0 | 2317 | 2 | 1 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0025 | 0/0 | 2319 | 2 | 0 | 0 | 2 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0026 | 0/0 | 2319 | 2 | 0 | 0 | 2 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0027 | 0/0 | 2319 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0028 | 0/0 | 2319 | 2 | 0 | 2 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0029 | 0/0 | 2318 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0030 | 0/0 | 2320 | 2 | 0 | 1 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0031 | 0/0 | 2319 | 2 | 1 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0032 | 0/0 | 2319 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0033 | 0/0 | 2319 | 2 | 0 | 0 | 1 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0034 | 0/0 | 2323 | 2 | 1 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0035 | 0/0 | 2315 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0036 | 0/0 | 2317 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0037 | 0/0 | 2317 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0038 | 0/0 | 2315 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0039 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0040 | 0/0 | 2316 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0041 | 0/0 | 2318 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0042 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0043 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0044 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0045 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0046 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0047 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0048 | 0/0 | 2320 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0049 | 0/0 | 2320 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0050 | 0/0 | 2318 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0051 | 0/0 | 2318 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0052 | 0/0 | 2318 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0053 | 0/0 | 2318 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0054 | 0/0 | 2318 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0055 | 1/0 | 2318 | 1 | 0 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0056 | 0/0 | 2318 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0057 | 0/0 | 2321 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0058 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0059 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0060 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0061 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0062 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0063 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0064 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0065 | 0/0 | 2317 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0066 | 0/0 | 2318 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0067 | 0/0 | 2320 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0068 | 0/0 | 2320 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0069 | 0/0 | 2320 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0070 | 0/0 | 2320 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0071 | 0/0 | 2318 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0072 | 0/0 | 2318 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0073 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0074 | 0/0 | 2321 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0075 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0076 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0077 | 0/0 | 2323 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| t0078 | 0/0 | 2323 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2211 | 180 | 53 | 40 | 51 | 13 | 22 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0003 | 0/0 | 2211 | 20 | 7 | 1 | 12 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0004 | 0/0 | 2211 | 6 | 0 | 0 | 6 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0006 | 0/0 | 2211 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0015 | 0/0 | 2211 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0016 | 0/0 | 2211 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002 | 1/0 | 2211 | 136 | 25 | 26 | 64 | 1 | 19 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0005 | 0/0 | 2211 | 3 | 2 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0007 | 0/0 | 2211 | 2 | 0 | 0 | 0 | 2 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0008 | 0/0 | 2211 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0011 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0017 | 0/0 | 2211 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0003c0014 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0004c0009 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0005c0010 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0006c0012 | 0/0 | 2211 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0007c0013 | 0/0 | 2186 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4529 | 60 | 17 | 12 | 21 | 1 | 8 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0003 | 0/0 | 4529 | 34 | 17 | 4 | 8 | 4 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0004 | 0/0 | 4530 | 20 | 1 | 9 | 5 | 2 | 3 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0006 | 0/0 | 4530 | 11 | 0 | 5 | 0 | 2 | 4 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0009 | 0/0 | 4529 | 8 | 0 | 0 | 8 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0011 | 0/0 | 4526 | 5 | 0 | 0 | 4 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0013 | 0/0 | 4529 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0014 | 0/0 | 4529 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0018 | 0/0 | 4530 | 2 | 0 | 1 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0021 | 0/0 | 4530 | 3 | 0 | 2 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0024 | 0/0 | 4527 | 2 | 1 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0025 | 0/0 | 4529 | 2 | 0 | 0 | 2 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0027 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0028 | 0/0 | 4529 | 2 | 0 | 2 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0031 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0032 | 0/0 | 4529 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0036 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0042 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0043 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0044 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0045 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0046 | 0/0 | 4529 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0047 | 0/0 | 4529 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0048 | 0/0 | 4530 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0057 | 0/0 | 4531 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0059 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0060 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0061 | 0/0 | 4529 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0062 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0063 | 0/0 | 4529 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0064 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0065 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0067 | 0/0 | 4530 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0068 | 0/0 | 4530 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0070 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0074 | 0/0 | 4531 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0075 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0076 | 0/0 | 4529 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0077 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0001t0078 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0003t0001 | 0/0 | 4529 | 12 | 2 | 0 | 10 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0003t0003 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0003t0004 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0003t0014 | 0/0 | 4529 | 3 | 3 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0003t0026 | 0/0 | 4529 | 2 | 0 | 0 | 2 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0003t0031 | 0/0 | 4529 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0004t0001 | 0/0 | 4529 | 5 | 0 | 0 | 5 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0004t0004 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0006t0001 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0006t0027 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0015t0001 | 0/0 | 4529 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0001c0016t0018 | 0/0 | 4530 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0002 | 0/0 | 4528 | 40 | 10 | 3 | 22 | 1 | 4 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0005 | 0/0 | 4528 | 19 | 0 | 7 | 9 | 0 | 3 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0007 | 0/0 | 4525 | 10 | 0 | 4 | 6 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0008 | 0/0 | 4529 | 8 | 0 | 1 | 6 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0010 | 0/0 | 4529 | 5 | 0 | 2 | 2 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0012 | 0/0 | 4525 | 5 | 0 | 0 | 5 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0013 | 0/0 | 4529 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0015 | 0/0 | 4530 | 4 | 2 | 0 | 0 | 0 | 2 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0016 | 0/0 | 4531 | 4 | 2 | 1 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0017 | 0/0 | 4526 | 3 | 0 | 0 | 3 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0019 | 0/0 | 4531 | 3 | 3 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0020 | 0/0 | 4529 | 3 | 0 | 0 | 2 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0022 | 0/0 | 4528 | 3 | 0 | 3 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0023 | 0/0 | 4530 | 3 | 1 | 1 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0029 | 0/0 | 4528 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0030 | 0/0 | 4530 | 2 | 0 | 1 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0033 | 0/0 | 4529 | 2 | 0 | 0 | 1 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0035 | 0/0 | 4525 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0038 | 0/0 | 4525 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0039 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0040 | 0/0 | 4526 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0041 | 0/0 | 4528 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0049 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0050 | 0/0 | 4528 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0051 | 0/0 | 4528 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0053 | 0/0 | 4528 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0054 | 0/0 | 4528 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0055 | 1/0 | 4528 | 1 | 0 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0056 | 0/0 | 4528 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0058 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0066 | 0/0 | 4528 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0069 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0071 | 0/0 | 4528 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0072 | 0/0 | 4528 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0002t0073 | 0/0 | 4529 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0005t0005 | 0/0 | 4528 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0005t0034 | 0/0 | 4533 | 2 | 1 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0007t0010 | 0/0 | 4529 | 2 | 0 | 0 | 0 | 2 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0008t0002 | 0/0 | 4528 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0008t0005 | 0/0 | 4528 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0011t0002 | 0/0 | 4528 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0002c0017t0052 | 0/0 | 4528 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0003c0014t0002 | 0/0 | 4528 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0004c0009t0008 | 0/0 | 4529 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0005c0010t0002 | 0/0 | 4528 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0006c0012t0037 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| a0007c0013t0004 | 0/0 | 4505 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | copy fasta | chr11 | 1384934 | 1467689 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0009g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0009g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0009g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0009g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0009g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0009g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0009g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0009g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0011g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0011g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0011g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0011g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0011g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0013g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0013g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0014g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0018g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0018g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0021g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0021g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0021g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0024g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0024g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0025g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0025g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0027g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0028g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0028g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0031g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0032g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0032g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0036g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0042g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0043g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0044g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0045g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0046g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0047g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0048g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0057g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0059g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0060g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0061g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0062g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0063g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0064g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0065g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0067g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0068g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0070g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0074g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0075g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0076g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0077g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0001t0078g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0014g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0026g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0026g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0003t0031g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0004t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0006t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0006t0027g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0015t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0001c0016t0018g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0007g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0007g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0007g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0007g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0007g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0007g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0007g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0007g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0007g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0008g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0008g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0008g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0008g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0008g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0010g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0010g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0010g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0010g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0012g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0012g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0012g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0012g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0013g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0015g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0015g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0015g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0015g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0016g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0016g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0016g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0016g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0017g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0017g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0017g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0019g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0019g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0019g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0020g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0020g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0020g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0022g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0022g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0023g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0023g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0023g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0029g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0029g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0030g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0030g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0033g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0033g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0035g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0038g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0039g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0040g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0041g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0049g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0050g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0051g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0053g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0054g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0055g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0056g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0058g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0066g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0069g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0071g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0072g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0002t0073g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0005t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0005t0034g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0005t0034g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0007t0010g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0007t0010g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0008t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0008t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0011t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0002c0017t0052g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0003c0014t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0004c0009t0008g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0005c0010t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0006c0012t0037g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| a0007c0013t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0011 | g0310 | EUR | GBR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0136 | EUR | GBR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0193 | EUR | FIN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0214 | EUR | FIN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00323 | hp2 | a0001 | c0001 | t0036 | g0300 | EUR | FIN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00408 | hp2 | a0002 | c0002 | t0008 | g0151 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0070 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00438 | hp1 | a0002 | c0002 | t0033 | g0279 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0138 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00558 | hp2 | a0001 | c0001 | t0025 | g0147 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00609 | hp2 | a0002 | c0002 | t0008 | g0157 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00639 | hp1 | a0001 | c0001 | t0063 | g0253 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00642 | hp1 | a0002 | c0002 | t0016 | g0240 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00642 | hp2 | a0001 | c0003 | t0031 | g0007 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0331 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00673 | hp2 | a0002 | c0002 | t0008 | g0071 | EAS | CHS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0197 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00735 | hp2 | a0002 | c0002 | t0005 | g0198 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00738 | hp1 | a0006 | c0012 | t0037 | g0293 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00738 | hp2 | a0002 | c0002 | t0073 | g0217 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00741 | hp1 | a0001 | c0001 | t0021 | g0221 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01070 | hp1 | a0002 | c0002 | t0010 | g0004 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01071 | hp2 | a0002 | c0002 | t0010 | g0004 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01081 | hp1 | a0002 | c0002 | t0030 | g0174 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01081 | hp2 | a0001 | c0001 | t0021 | g0206 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01099 | hp1 | a0002 | c0002 | t0008 | g0116 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0170 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01109 | hp1 | a0002 | c0002 | t0005 | g0216 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01167 | hp2 | a0002 | c0002 | t0023 | g0223 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0247 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01175 | hp2 | a0002 | c0002 | t0005 | g0276 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01192 | hp1 | a0001 | c0001 | t0014 | g0039 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01243 | hp2 | a0001 | c0001 | t0047 | g0340 | AMR | PUR | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01255 | hp1 | a0002 | c0002 | t0071 | g0249 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01255 | hp2 | a0001 | c0001 | t0068 | g0243 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0106 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01256 | hp2 | a0002 | c0002 | t0022 | g0003 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01257 | hp1 | a0001 | c0001 | t0028 | g0332 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01258 | hp1 | a0001 | c0001 | t0028 | g0333 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01258 | hp2 | a0002 | c0002 | t0022 | g0003 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0215 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01261 | hp2 | a0001 | c0001 | t0018 | g0137 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01346 | hp1 | a0002 | c0002 | t0005 | g0260 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01346 | hp2 | a0002 | c0005 | t0034 | g0056 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0225 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0179 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01433 | hp1 | a0001 | c0015 | t0001 | g0315 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01433 | hp2 | a0002 | c0017 | t0052 | g0008 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0169 | EUR | IBS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01515 | hp2 | a0002 | c0007 | t0010 | g0245 | EUR | IBS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0227 | EUR | IBS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0220 | EUR | IBS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0219 | EUR | IBS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01517 | hp2 | a0002 | c0007 | t0010 | g0244 | EUR | IBS | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01884 | hp1 | a0002 | c0008 | t0005 | g0278 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01884 | hp2 | a0001 | c0001 | t0032 | g0195 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01891 | hp1 | a0002 | c0002 | t0049 | g0117 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01934 | hp1 | a0002 | c0002 | t0005 | g0283 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0314 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01952 | hp1 | a0002 | c0002 | t0005 | g0277 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0318 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01975 | hp2 | a0002 | c0002 | t0007 | g0294 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01978 | hp1 | a0002 | c0002 | t0007 | g0309 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0316 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01981 | hp1 | a0001 | c0001 | t0076 | g0182 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01993 | hp1 | a0002 | c0002 | t0005 | g0281 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0180 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02004 | hp2 | a0002 | c0002 | t0022 | g0204 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02027 | hp1 | a0002 | c0002 | t0005 | g0258 | EAS | KHV | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02027 | hp2 | a0001 | c0001 | t0046 | g0083 | EAS | KHV | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | KHV | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02040 | hp2 | a0002 | c0002 | t0056 | g0337 | EAS | KHV | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02055 | hp1 | a0001 | c0001 | t0064 | g0261 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0159 | EAS | KHV | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02074 | hp2 | a0002 | c0002 | t0051 | g0077 | EAS | KHV | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0320 | EAS | KHV | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | KHV | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0321 | EAS | KHV | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02132 | hp1 | a0002 | c0002 | t0005 | g0259 | EAS | KHV | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02132 | hp2 | a0002 | c0002 | t0005 | g0269 | EAS | KHV | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | CDX | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02165 | hp1 | a0002 | c0002 | t0010 | g0233 | EAS | CDX | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | CDX | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02257 | hp1 | a0002 | c0002 | t0015 | g0028 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02257 | hp2 | a0001 | c0001 | t0027 | g0129 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02258 | hp1 | a0002 | c0002 | t0015 | g0330 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02258 | hp2 | a0002 | c0002 | t0029 | g0025 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02273 | hp1 | a0001 | c0016 | t0018 | g0183 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02273 | hp2 | a0002 | c0002 | t0007 | g0304 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02280 | hp1 | a0002 | c0002 | t0019 | g0021 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02280 | hp2 | a0002 | c0002 | t0058 | g0325 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02293 | hp1 | a0002 | c0002 | t0035 | g0296 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02300 | hp2 | a0002 | c0002 | t0007 | g0308 | AMR | PEL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0020 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02602 | hp1 | a0001 | c0001 | t0021 | g0242 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02602 | hp2 | a0002 | c0002 | t0038 | g0297 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02630 | hp1 | a0001 | c0001 | t0075 | g0202 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0311 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02647 | hp1 | a0001 | c0001 | t0043 | g0050 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02647 | hp2 | a0002 | c0002 | t0016 | g0207 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0172 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0248 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02698 | hp2 | a0002 | c0002 | t0005 | g0212 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02717 | hp1 | a0002 | c0005 | t0034 | g0055 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0024 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0229 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0251 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02738 | hp1 | a0001 | c0001 | t0057 | g0184 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02738 | hp2 | a0002 | c0002 | t0033 | g0286 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0035 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02895 | hp1 | a0001 | c0001 | t0070 | g0210 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02895 | hp2 | a0002 | c0002 | t0069 | g0231 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0146 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02897 | hp2 | a0001 | c0001 | t0032 | g0209 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02922 | hp1 | a0001 | c0003 | t0014 | g0038 | AFR | ESN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ESN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0126 | AFR | ESN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02976 | hp1 | a0001 | c0001 | t0045 | g0040 | AFR | ESN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | ESN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03017 | hp2 | a0002 | c0002 | t0008 | g0167 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03041 | hp1 | a0001 | c0006 | t0001 | g0047 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0291 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03098 | hp1 | a0002 | c0002 | t0029 | g0026 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03130 | hp1 | a0001 | c0001 | t0077 | g0324 | AFR | ESN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03195 | hp1 | a0001 | c0003 | t0014 | g0037 | AFR | ESN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03195 | hp2 | a0002 | c0008 | t0002 | g0326 | AFR | ESN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03225 | hp1 | a0002 | c0002 | t0019 | g0043 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0173 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03239 | hp2 | a0002 | c0002 | t0023 | g0254 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03486 | hp1 | a0002 | c0011 | t0002 | g0032 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03492 | hp1 | a0002 | c0002 | t0066 | g0285 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03516 | hp1 | a0001 | c0001 | t0042 | g0160 | AFR | ESN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | ESN | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03540 | hp1 | a0002 | c0002 | t0019 | g0042 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03579 | hp1 | a0002 | c0005 | t0005 | g0289 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03579 | hp2 | a0001 | c0003 | t0014 | g0036 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0176 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03654 | hp2 | a0001 | c0001 | t0078 | g0205 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03688 | hp1 | a0002 | c0002 | t0005 | g0224 | SAS | STU | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03688 | hp2 | a0002 | c0002 | t0005 | g0250 | SAS | STU | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03704 | hp1 | a0002 | c0002 | t0020 | g0125 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03831 | hp1 | a0002 | c0002 | t0030 | g0171 | SAS | BEB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03831 | hp2 | a0002 | c0002 | t0040 | g0298 | SAS | BEB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0119 | SAS | BEB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0323 | SAS | BEB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03942 | hp1 | a0001 | c0001 | t0067 | g0252 | SAS | BEB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0218 | SAS | BEB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG04115 | hp1 | a0002 | c0002 | t0016 | g0284 | SAS | STU | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG04115 | hp2 | a0001 | c0001 | t0074 | g0213 | SAS | STU | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG04184 | hp1 | a0004 | c0009 | t0008 | g0178 | SAS | BEB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0280 | SAS | BEB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG04199 | hp2 | a0002 | c0002 | t0015 | g0327 | SAS | STU | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG04204 | hp1 | a0002 | c0002 | t0015 | g0027 | SAS | STU | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG04204 | hp2 | a0002 | c0002 | t0010 | g0246 | SAS | STU | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG04228 | hp2 | a0001 | c0001 | t0018 | g0334 | SAS | STU | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18522 | hp1 | a0001 | c0001 | t0013 | g0022 | AFR | YRI | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18522 | hp2 | a0001 | c0001 | t0060 | g0163 | AFR | YRI | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18612 | hp1 | a0002 | c0002 | t0050 | g0165 | EAS | CHB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18612 | hp2 | a0001 | c0001 | t0009 | g0153 | EAS | CHB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18906 | hp1 | a0001 | c0001 | t0044 | g0016 | AFR | YRI | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18906 | hp2 | a0001 | c0006 | t0027 | g0142 | AFR | YRI | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18939 | hp1 | a0002 | c0002 | t0072 | g0273 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18940 | hp2 | a0001 | c0004 | t0001 | g0096 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18944 | hp2 | a0002 | c0002 | t0005 | g0264 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0135 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18947 | hp2 | a0002 | c0002 | t0008 | g0162 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18950 | hp2 | a0002 | c0002 | t0012 | g0349 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18952 | hp2 | a0001 | c0001 | t0011 | g0295 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18953 | hp1 | a0002 | c0002 | t0010 | g0275 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18953 | hp2 | a0007 | c0013 | t0004 | g0065 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0341 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18956 | hp2 | a0002 | c0002 | t0008 | g0078 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18959 | hp2 | a0002 | c0002 | t0020 | g0148 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18963 | hp2 | a0001 | c0001 | t0065 | g0256 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18964 | hp1 | a0001 | c0001 | t0009 | g0187 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18966 | hp1 | a0001 | c0001 | t0009 | g0101 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18966 | hp2 | a0002 | c0002 | t0017 | g0301 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18967 | hp1 | a0002 | c0002 | t0005 | g0262 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18969 | hp2 | a0001 | c0004 | t0001 | g0095 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18970 | hp1 | a0002 | c0002 | t0007 | g0350 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18971 | hp1 | a0001 | c0003 | t0026 | g0354 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18973 | hp1 | a0002 | c0002 | t0041 | g0144 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0338 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18975 | hp1 | a0001 | c0001 | t0009 | g0068 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18975 | hp2 | a0002 | c0002 | t0017 | g0353 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18977 | hp2 | a0002 | c0002 | t0039 | g0344 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18980 | hp2 | a0001 | c0001 | t0011 | g0303 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18982 | hp1 | a0005 | c0010 | t0002 | g0085 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18982 | hp2 | a0002 | c0002 | t0005 | g0274 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18983 | hp1 | a0002 | c0002 | t0012 | g0348 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0134 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18990 | hp2 | a0002 | c0002 | t0007 | g0306 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18993 | hp1 | a0002 | c0002 | t0017 | g0305 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18993 | hp2 | a0001 | c0004 | t0001 | g0094 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18994 | hp1 | a0001 | c0001 | t0011 | g0307 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18995 | hp1 | a0001 | c0001 | t0009 | g0100 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18995 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18999 | hp2 | a0001 | c0001 | t0009 | g0128 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19000 | hp1 | a0001 | c0001 | t0009 | g0122 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19000 | hp2 | a0002 | c0002 | t0007 | g0346 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19002 | hp2 | a0002 | c0002 | t0007 | g0351 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19005 | hp1 | a0002 | c0002 | t0012 | g0006 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19007 | hp2 | a0002 | c0002 | t0053 | g0139 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19009 | hp1 | a0002 | c0002 | t0020 | g0156 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19009 | hp2 | a0001 | c0004 | t0001 | g0093 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19011 | hp1 | a0002 | c0002 | t0008 | g0181 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19012 | hp2 | a0001 | c0004 | t0004 | g0092 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19030 | hp1 | a0002 | c0002 | t0023 | g0255 | AFR | LWK | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0287 | AFR | LWK | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0115 | AFR | LWK | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19043 | hp2 | a0001 | c0001 | t0031 | g0012 | AFR | LWK | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19054 | hp2 | a0002 | c0002 | t0012 | g0006 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19060 | hp2 | a0002 | c0002 | t0007 | g0345 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19067 | hp1 | a0003 | c0014 | t0002 | g0319 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19068 | hp1 | a0001 | c0004 | t0001 | g0091 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19068 | hp2 | a0002 | c0002 | t0054 | g0322 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19070 | hp1 | a0002 | c0002 | t0007 | g0302 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19074 | hp1 | a0001 | c0001 | t0009 | g0120 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19079 | hp1 | a0002 | c0002 | t0005 | g0211 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0336 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19080 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19083 | hp1 | a0002 | c0002 | t0012 | g0347 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19083 | hp2 | a0001 | c0003 | t0001 | g0335 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19088 | hp1 | a0001 | c0001 | t0025 | g0143 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19088 | hp2 | a0001 | c0001 | t0061 | g0266 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | YRI | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0033 | AFR | YRI | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA20129 | hp1 | a0001 | c0003 | t0004 | g0290 | AFR | ASW | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA20129 | hp2 | a0002 | c0002 | t0013 | g0001 | AFR | ASW | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA20752 | hp1 | a0001 | c0001 | t0024 | g0299 | EUR | TSI | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0190 | EUR | TSI | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA20805 | hp1 | a0001 | c0001 | t0048 | g0342 | EUR | TSI | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0226 | EUR | TSI | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0118 | SAS | GIH | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0188 | SAS | GIH | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0282 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02486 | hp1 | a0001 | c0001 | t0062 | g0257 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | ACB | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03471 | hp1 | a0002 | c0002 | t0016 | g0208 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | USA | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | USA | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18955 | hp1 | a0001 | c0001 | t0011 | g0352 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA18955 | hp2 | a0001 | c0003 | t0026 | g0054 | EAS | JPT | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA20300 | hp1 | a0002 | c0002 | t0013 | g0001 | AFR | USA | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | USA | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA21309 | hp1 | a0001 | c0001 | t0059 | g0041 | AFR | LWK | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| NA21309 | hp2 | a0001 | c0001 | t0024 | g0292 | AFR | LWK | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0141 | REF | REF | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0055 | g0131 | REF | REF | BRSK2_chr11_1384934_1467689 | BRSK2 | chr11 | 1384934 | 1467689 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1450675
|
C | T | 1 | a0003 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.1376C>T | p.Thr459Met | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 14/20 | 1727/4528 | 1376/2211 | 459/736 | chr11 | 1450675 | ||
| chr11:1456402
|
AAGGCCAC others(18): Show |
A | 1 | a0007 | 1 | NA18953.hp2 | frameshift_variant | HIGH | c.1724_1748delAGGCCA others(19): Show |
p.Lys575fs | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 17/20 | 2075/4528 | 1724/2211 | 575/736 | chr11 | 1456402 | ||
| chr11:1456412
|
G | C | 1 | a0004 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.1733G>C | p.Gly578Ala | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 17/20 | 2084/4528 | 1733/2211 | 578/736 | chr11 | 1456412 | ||
| chr11:1456652
|
G | A | 1 | a0005 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1904G>A | p.Ser635Asn | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/20 | 2255/4528 | 1904/2211 | 635/736 | chr11 | 1456652 | ||
| chr11:1460695
|
C | T | 1 | a0006 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.2183C>T | p.Pro728Leu | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 2534/4528 | 2183/2211 | 728/736 | chr11 | 1460695 | ||
| chr11:1460700
|
A | G | 2 | a0001a0007 | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
missense_variant | MODERATE | c.2188A>G | p.Thr730Ala | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 2539/4528 | 2188/2211 | 730/736 | chr11 | 1460700 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1436065
|
C | T | 1 | a0002c0017 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.117C>T | p.Cys39Cys | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/20 | 468/4528 | 117/2211 | 39/736 | chr11 | 1436065 | ||
| chr11:1442526
|
C | T | 1 | a0001c0016 | 1 | HG02273.hp1 | synonymous_variant | LOW | c.450C>T | p.Asp150Asp | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 5/20 | 801/4528 | 450/2211 | 150/736 | chr11 | 1442526 | ||
| chr11:1442565
|
G | A | 1 | a0001c0006 | 2 | HG03041.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.489G>A | p.Ala163Ala | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 5/20 | 840/4528 | 489/2211 | 163/736 | chr11 | 1442565 | ||
| chr11:1445381
|
C | T | 2 | a0001c0004a0002c0008 | 8 | HG01884.hp1 HG03195.hp2 NA18940.hp2 others(5): Show |
synonymous_variant | LOW | c.900C>T | p.Pro300Pro | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 10/20 | 1251/4528 | 900/2211 | 300/736 | chr11 | 1445381 | ||
| chr11:1445824
|
A | G | 4 | a0001c0003a0001c0004a0001c0015others(1): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
synonymous_variant | LOW | c.1143A>G | p.Lys381Lys | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/20 | 1494/4528 | 1143/2211 | 381/736 | chr11 | 1445824 | ||
| chr11:1451381
|
G | A | 1 | a0002c0007 | 2 | HG01515.hp2 HG01517.hp2 |
synonymous_variant | LOW | c.1506G>A | p.Pro502Pro | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/20 | 1857/4528 | 1506/2211 | 502/736 | chr11 | 1451381 | ||
| chr11:1456647
|
G | A | 1 | a0001c0015 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.1899G>A | p.Leu633Leu | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/20 | 2250/4528 | 1899/2211 | 633/736 | chr11 | 1456647 | ||
| chr11:1456683
|
G | A | 1 | a0002c0011 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1935G>A | p.Leu645Leu | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/20 | 2286/4528 | 1935/2211 | 645/736 | chr11 | 1456683 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1390000
|
T | TCGG | 3 | a0001c0001t0077a0001c0001t0078a0002c0005t0034 | 4 | HG01346.hp2 HG02717.hp1 HG03130.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-260_-258dupCGG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/20 | 257 | INFO_REALIGN_3_PRIME | chr11 | 1390000 | ||||
| chr11:1390000
|
TCGG | T | 11 | a0001c0001t0011a0001c0001t0024a0001c0001t0036others(8): Show | 31 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-260_-258delCGG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/20 | 258 | INFO_REALIGN_3_PRIME | chr11 | 1390000 | ||||
| chr11:1390028
|
A | C | 1 | a0001c0001t0076 | 1 | HG01981.hp1 | 5_prime_UTR_variant | MODIFIER | c.-257A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/20 | 257 | chr11 | 1390028 | |||||
| chr11:1390090
|
C | A | 3 | a0001c0001t0025a0001c0003t0026a0002c0002t0041 | 5 | HG00558.hp2 NA18955.hp2 NA18971.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-195C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/20 | 195 | chr11 | 1390090 | |||||
| chr11:1390111
|
T | TGGACGCG others(14): Show |
1 | a0001c0001t0043 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-166_-165insAGGGCG others(15): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/20 | 165 | INFO_REALIGN_3_PRIME | chr11 | 1390111 | ||||
| chr11:1390119
|
G | C | 3 | a0001c0001t0027a0001c0001t0042a0001c0006t0027 | 3 | HG02257.hp2 HG03516.hp1 NA18906.hp2 |
5_prime_UTR_variant | MODIFIER | c.-166G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/20 | 166 | chr11 | 1390119 | |||||
| chr11:1390271
|
C | T | 41 | a0001c0001t0003a0001c0001t0006a0001c0001t0011others(38): Show | 138 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-14C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/20 | chr11 | 1390271 | ||||||
| chr11:1460732
|
G | GC | 14 | a0001c0001t0042a0001c0001t0057a0001c0001t0059others(11): Show | 24 | HG00438.hp1 HG00642.hp1 HG00738.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*20dupC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 21 | INFO_REALIGN_3_PRIME | chr11 | 1460732 | ||||
| chr11:1460732
|
GC | G | 37 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(34): Show | 175 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*20delC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 20 | INFO_REALIGN_3_PRIME | chr11 | 1460732 | ||||
| chr11:1460739
|
C | A | 1 | a0002c0002t0035 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*16C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 16 | chr11 | 1460739 | |||||
| chr11:1460743
|
C | G | 3 | a0001c0001t0031a0001c0001t0075a0001c0003t0031 | 3 | HG00642.hp2 HG02630.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*20C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 20 | chr11 | 1460743 | |||||
| chr11:1460776
|
C | T | 1 | a0002c0002t0056 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 53 | chr11 | 1460776 | |||||
| chr11:1460784
|
G | A | 5 | a0001c0001t0018a0001c0001t0021a0001c0001t0036others(2): Show | 8 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*61G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 61 | chr11 | 1460784 | |||||
| chr11:1460784
|
G | C | 1 | a0001c0001t0067 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*61G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 61 | chr11 | 1460784 | |||||
| chr11:1460810
|
G | A | 1 | a0002c0002t0029 | 2 | HG02258.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*87G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 87 | chr11 | 1460810 | |||||
| chr11:1460810
|
G | T | 3 | a0001c0001t0031a0001c0001t0075a0001c0003t0031 | 3 | HG00642.hp2 HG02630.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*87G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 87 | chr11 | 1460810 | |||||
| chr11:1460872
|
C | T | 1 | a0002c0002t0072 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*149C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 149 | chr11 | 1460872 | |||||
| chr11:1461086
|
C | A | 1 | a0002c0002t0039 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*363C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 363 | chr11 | 1461086 | |||||
| chr11:1461087
|
A | G | 1 | a0002c0002t0039 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*364A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 364 | chr11 | 1461087 | |||||
| chr11:1461088
|
G | C | 1 | a0002c0002t0039 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*365G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 365 | chr11 | 1461088 | |||||
| chr11:1461105
|
C | T | 1 | a0001c0001t0047 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*382C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 382 | chr11 | 1461105 | |||||
| chr11:1461120
|
T | C | 2 | a0002c0002t0022a0002c0002t0073 | 4 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*397T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 397 | chr11 | 1461120 | |||||
| chr11:1461133
|
G | A | 1 | a0001c0001t0061 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*410G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 410 | chr11 | 1461133 | |||||
| chr11:1461164
|
G | A | 1 | a0001c0001t0028 | 2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*441G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 441 | chr11 | 1461164 | |||||
| chr11:1461202
|
C | T | 1 | a0002c0005t0034 | 2 | HG01346.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*479C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 479 | chr11 | 1461202 | |||||
| chr11:1461227
|
C | A | 1 | a0001c0001t0062 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*504C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 504 | chr11 | 1461227 | |||||
| chr11:1461252
|
G | A | 1 | a0001c0001t0009 | 8 | NA18612.hp2 NA18964.hp1 NA18966.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*529G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 529 | chr11 | 1461252 | |||||
| chr11:1461258
|
T | C | 68 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(65): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*535T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 535 | chr11 | 1461258 | |||||
| chr11:1461352
|
T | C | 95 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(92): Show | 356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
3_prime_UTR_variant | MODIFIER | c.*629T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 629 | chr11 | 1461352 | |||||
| chr11:1461395
|
G | A | 1 | a0002c0002t0030 | 2 | HG01081.hp1 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*672G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 672 | chr11 | 1461395 | |||||
| chr11:1461490
|
C | T | 42 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(39): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*767C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 767 | chr11 | 1461490 | |||||
| chr11:1461621
|
T | C | 56 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(53): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*898T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 898 | chr11 | 1461621 | |||||
| chr11:1461635
|
G | C | 4 | a0001c0001t0013a0001c0001t0032a0001c0001t0070others(1): Show | 7 | HG01884.hp2 HG02630.hp2 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*912G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 912 | chr11 | 1461635 | |||||
| chr11:1461688
|
G | T | 1 | a0001c0001t0063 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*965G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 965 | chr11 | 1461688 | |||||
| chr11:1461695
|
G | T | 2 | a0001c0001t0042a0001c0001t0060 | 2 | HG03516.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*972G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 972 | chr11 | 1461695 | |||||
| chr11:1461752
|
T | C | 1 | a0002c0002t0051 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1029T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1029 | chr11 | 1461752 | |||||
| chr11:1461887
|
G | GTC | 67 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(64): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*1170_*1171dupCT | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1172 | INFO_REALIGN_3_PRIME | chr11 | 1461887 | ||||
| chr11:1461922
|
G | T | 1 | a0001c0001t0065 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1199G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1199 | chr11 | 1461922 | |||||
| chr11:1461947
|
T | C | 95 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(92): Show | 356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
3_prime_UTR_variant | MODIFIER | c.*1224T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1224 | chr11 | 1461947 | |||||
| chr11:1461950
|
A | G | 5 | a0001c0001t0018a0001c0001t0021a0001c0001t0036others(2): Show | 8 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1227A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1227 | chr11 | 1461950 | |||||
| chr11:1461953
|
G | C | 1 | a0001c0001t0044 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1230G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1230 | chr11 | 1461953 | |||||
| chr11:1461968
|
C | T | 3 | a0001c0001t0042a0001c0001t0059a0001c0001t0060 | 3 | HG03516.hp1 NA18522.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1245C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1245 | chr11 | 1461968 | |||||
| chr11:1462062
|
G | A | 2 | a0002c0002t0023a0002c0002t0049 | 4 | HG01167.hp2 HG01891.hp1 HG03239.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1339G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1339 | chr11 | 1462062 | |||||
| chr11:1462068
|
G | A | 1 | a0001c0001t0045 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1345G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1345 | chr11 | 1462068 | |||||
| chr11:1462173
|
G | T | 3 | a0001c0001t0042a0001c0001t0059a0001c0001t0060 | 3 | HG03516.hp1 NA18522.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1450G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1450 | chr11 | 1462173 | |||||
| chr11:1462214
|
G | A | 1 | a0001c0001t0046 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1491G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1491 | chr11 | 1462214 | |||||
| chr11:1462299
|
G | A | 1 | a0002c0002t0019 | 3 | HG02280.hp1 HG03225.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1576G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1576 | chr11 | 1462299 | |||||
| chr11:1462301
|
C | T | 1 | a0001c0003t0026 | 2 | NA18955.hp2 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1578C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1578 | chr11 | 1462301 | |||||
| chr11:1462306
|
G | A | 1 | a0002c0017t0052 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1583G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1583 | chr11 | 1462306 | |||||
| chr11:1462313
|
A | G | 67 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(64): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*1590A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1590 | chr11 | 1462313 | |||||
| chr11:1462380
|
C | T | 1 | a0002c0002t0054 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1657C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1657 | chr11 | 1462380 | |||||
| chr11:1462485
|
C | T | 1 | a0002c0002t0053 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1762C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1762 | chr11 | 1462485 | |||||
| chr11:1462526
|
G | A | 2 | a0001c0001t0014a0001c0003t0014 | 4 | HG01192.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1803G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 20/20 | 1803 | chr11 | 1462526 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1390425
|
C | A | 38 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(35): Show | 39 | HG00642.hp2 HG01109.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.91+50C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1390425 | ||||||
| chr11:1390699
|
A | T | 1 | a0001c0003t0026g0354 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.91+324A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1390699 | ||||||
| chr11:1390783
|
C | T | 11 | a0001c0001t0011g0352a0002c0002t0007g0345a0002c0002t0007g0346others(8): Show | 12 | NA18950.hp2 NA18955.hp1 NA18970.hp1 others(9): Show |
intron_variant | MODIFIER | c.91+408C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1390783 | ||||||
| chr11:1390830
|
G | T | 3 | a0001c0001t0059g0041a0002c0002t0019g0042a0002c0002t0019g0043 | 3 | HG03225.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.91+455G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1390830 | ||||||
| chr11:1390840
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.91+465G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1390840 | ||||||
| chr11:1391089
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.91+714G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391089 | ||||||
| chr11:1391162
|
C | T | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+787C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391162 | ||||||
| chr11:1391164
|
C | G | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91+789C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391164 | ||||||
| chr11:1391167
|
C | G | 3 | a0001c0001t0001g0328a0001c0001t0001g0329a0002c0002t0015g0327 | 3 | HG03017.hp1 HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.91+792C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391167 | ||||||
| chr11:1391206
|
A | G | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+831A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391206 | ||||||
| chr11:1391239
|
C | T | 1 | a0002c0008t0002g0326 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.91+864C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391239 | ||||||
| chr11:1391340
|
C | T | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+965C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391340 | ||||||
| chr11:1391380
|
G | A | 8 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(5): Show | 8 | HG01243.hp1 HG01943.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.91+1005G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391380 | ||||||
| chr11:1391422
|
G | A | 1 | a0001c0003t0026g0054 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.91+1047G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391422 | ||||||
| chr11:1391481
|
G | A | 1 | a0001c0003t0031g0007 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.91+1106G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391481 | ||||||
| chr11:1391607
|
C | T | 39 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(36): Show | 40 | HG00642.hp2 HG01109.hp2 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.91+1232C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391607 | ||||||
| chr11:1391618
|
A | G | 164 | a0001c0001t0001g0044a0001c0001t0001g0312a0001c0001t0001g0313others(161): Show | 169 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.91+1243A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391618 | ||||||
| chr11:1391826
|
T | C | 164 | a0001c0001t0001g0044a0001c0001t0001g0312a0001c0001t0001g0313others(161): Show | 169 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.91+1451T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391826 | ||||||
| chr11:1391828
|
C | T | 151 | a0001c0001t0001g0044a0001c0001t0001g0312a0001c0001t0001g0313others(148): Show | 156 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.91+1453C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391828 | ||||||
| chr11:1391901
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.91+1526T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1391901 | ||||||
| chr11:1392005
|
T | G | 101 | a0001c0001t0003g0002a0001c0001t0003g0045a0001c0001t0003g0193others(98): Show | 105 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.91+1630T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392005 | ||||||
| chr11:1392018
|
G | T | 2 | a0001c0001t0014g0039a0001c0001t0045g0040 | 2 | HG01192.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.91+1643G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392018 | ||||||
| chr11:1392022
|
G | A | 2 | a0002c0005t0034g0055a0002c0005t0034g0056 | 2 | HG01346.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.91+1647G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392022 | ||||||
| chr11:1392093
|
C | T | 38 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(35): Show | 39 | HG00642.hp2 HG01109.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.91+1718C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392093 | ||||||
| chr11:1392222
|
A | G | 1 | a0001c0001t0003g0288 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.91+1847A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392222 | ||||||
| chr11:1392243
|
G | A | 1 | a0001c0001t0003g0193 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.91+1868G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392243 | ||||||
| chr11:1392347
|
T | C | 60 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.91+1972T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392347 | ||||||
| chr11:1392370
|
G | A | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91+1995G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392370 | ||||||
| chr11:1392409
|
C | T | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+2034C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392409 | ||||||
| chr11:1392427
|
C | T | 32 | a0001c0001t0003g0263a0001c0001t0003g0265a0001c0001t0003g0267others(29): Show | 33 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.91+2052C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392427 | ||||||
| chr11:1392532
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.91+2157G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392532 | ||||||
| chr11:1392586
|
G | A | 150 | a0001c0001t0001g0044a0001c0001t0001g0312a0001c0001t0001g0313others(147): Show | 155 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.91+2211G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392586 | ||||||
| chr11:1392635
|
G | A | 1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.91+2260G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392635 | ||||||
| chr11:1392665
|
G | A | 1 | a0001c0001t0003g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+2290G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392665 | ||||||
| chr11:1392686
|
A | G | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+2311A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392686 | ||||||
| chr11:1392709
|
G | A | 1 | a0001c0001t0032g0195 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.91+2334G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392709 | ||||||
| chr11:1392744
|
T | G | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.91+2369T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392744 | ||||||
| chr11:1392795
|
C | G | 297 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(294): Show | 303 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.91+2420C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392795 | ||||||
| chr11:1392837
|
C | T | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+2462C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392837 | ||||||
| chr11:1392884
|
C | T | 1 | a0001c0001t0065g0256 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.91+2509C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392884 | ||||||
| chr11:1392944
|
C | T | 1 | a0001c0001t0003g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+2569C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1392944 | ||||||
| chr11:1393045
|
C | T | 13 | a0001c0001t0001g0044a0001c0001t0001g0313a0001c0001t0001g0317others(10): Show | 13 | HG01433.hp1 HG01943.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.91+2670C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393045 | ||||||
| chr11:1393174
|
C | T | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91+2799C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393174 | ||||||
| chr11:1393235
|
TTTTGTCC others(9): Show |
T | 17 | a0001c0001t0001g0044a0001c0001t0001g0312a0001c0001t0001g0313others(14): Show | 17 | HG01433.hp1 HG01943.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.91+2871_91+2886del others(16): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1393235 | |||||
| chr11:1393242
|
C | T | 2 | a0002c0002t0033g0286a0002c0002t0066g0285 | 2 | HG02738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.91+2867C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393242 | ||||||
| chr11:1393249
|
G | A | 1 | a0001c0001t0062g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.91+2874G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393249 | ||||||
| chr11:1393265
|
C | T | 38 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(35): Show | 39 | HG00642.hp2 HG01109.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.91+2890C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393265 | ||||||
| chr11:1393350
|
G | A | 23 | a0001c0001t0001g0186a0001c0001t0001g0189a0001c0001t0001g0191others(20): Show | 23 | HG01069.hp1 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.91+2975G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393350 | ||||||
| chr11:1393375
|
T | G | 2 | a0001c0001t0003g0194a0001c0001t0003g0196 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.91+3000T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393375 | ||||||
| chr11:1393392
|
G | A | 1 | a0001c0003t0001g0114 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.91+3017G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393392 | ||||||
| chr11:1393455
|
C | T | 2 | a0001c0001t0001g0168a0002c0002t0015g0330 | 2 | HG02155.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.91+3080C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393455 | ||||||
| chr11:1393475
|
C | T | 17 | a0001c0001t0001g0044a0001c0001t0001g0312a0001c0001t0001g0313others(14): Show | 17 | HG01433.hp1 HG01943.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.91+3100C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393475 | ||||||
| chr11:1393562
|
T | G | 1 | a0002c0017t0052g0008 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.91+3187T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393562 | ||||||
| chr11:1393563
|
G | T | 1 | a0002c0017t0052g0008 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.91+3188G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393563 | ||||||
| chr11:1393576
|
A | G | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3201A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393576 | ||||||
| chr11:1393824
|
C | T | 5 | a0001c0003t0014g0036a0001c0003t0014g0037a0001c0003t0014g0038others(2): Show | 5 | HG00642.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+3449C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393824 | ||||||
| chr11:1393832
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.91+3457G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393832 | ||||||
| chr11:1393892
|
T | TCCTGGAG others(99): Show |
4 | a0001c0001t0001g0009a0001c0001t0014g0039a0001c0001t0045g0040others(1): Show | 4 | HG01192.hp1 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+3596_91+3701dup others(106): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1393892 | |||||
| chr11:1393921
|
A | ATGGAGAT others(99): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02055.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.91+3595_91+3596ins others(106): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1393921 | |||||
| chr11:1393921
|
A | ATGGAGAT others(112): Show |
29 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0029others(26): Show | 30 | HG00642.hp2 HG01109.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.91+3583_91+3701dup others(119): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1393921 | |||||
| chr11:1393921
|
A | ATGGAGAT others(112): Show |
1 | a0001c0001t0001g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.91+3649_91+3650ins others(119): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1393921 | |||||
| chr11:1393921
|
ATGGAGAT others(6): Show |
A | 152 | a0001c0001t0001g0044a0001c0001t0001g0312a0001c0001t0001g0313others(149): Show | 157 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.91+3596_91+3608del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1393921 | |||||
| chr11:1393944
|
G | GC | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3569_91+3570ins others(1): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393944 | ||||||
| chr11:1393945
|
T | C | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3570T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393945 | ||||||
| chr11:1393958
|
T | C | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3583T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393958 | ||||||
| chr11:1393960
|
C | A | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3585C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393960 | ||||||
| chr11:1393966
|
A | G | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3591A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393966 | ||||||
| chr11:1393971
|
T | C | 1 | a0001c0001t0006g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.91+3596T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393971 | ||||||
| chr11:1393973
|
C | A | 1 | a0001c0001t0006g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.91+3598C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393973 | ||||||
| chr11:1393973
|
CTGGAGAT others(6): Show |
C | 9 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(6): Show | 9 | HG01243.hp1 HG01943.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.91+3609_91+3621del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1393973 | |||||
| chr11:1393984
|
C | T | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3609C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393984 | ||||||
| chr11:1393986
|
A | ATGGAGAT others(86): Show |
1 | a0001c0001t0031g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.91+3701_91+3702ins others(93): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1393986 | |||||
| chr11:1393986
|
A | C | 14 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0006g0197others(11): Show | 14 | HG00673.hp1 HG00735.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.91+3611A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393986 | ||||||
| chr11:1393996
|
GT | G | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3622delT | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393996 | ||||||
| chr11:1393997
|
T | C | 1 | a0001c0001t0006g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.91+3622T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1393997 | ||||||
| chr11:1394000
|
C | A | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3625C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394000 | ||||||
| chr11:1394011
|
C | CCATGGAG others(58): Show |
1 | a0001c0001t0006g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.91+3637_91+3638ins others(65): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394011 | |||||
| chr11:1394011
|
C | CCCCTGGA others(72): Show |
3 | a0001c0001t0063g0253a0002c0002t0023g0254a0002c0002t0023g0255 | 3 | HG00639.hp1 HG03239.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.91+3689_91+3767dup others(79): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394011 | |||||
| chr11:1394011
|
C | T | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3636C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394011 | ||||||
| chr11:1394024
|
G | GC | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3651dupC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394024 | |||||
| chr11:1394027
|
A | C | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3652A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394027 | ||||||
| chr11:1394027
|
ATGGAGAT others(6): Show |
A | 1 | a0002c0002t0049g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.91+3689_91+3701del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394027 | |||||
| chr11:1394038
|
T | C | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3663T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394038 | ||||||
| chr11:1394040
|
C | A | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3665C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394040 | ||||||
| chr11:1394051
|
T | TCCTGGAG others(112): Show |
1 | a0002c0017t0052g0008 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.91+3701_91+3702ins others(119): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394051 | |||||
| chr11:1394059
|
A | G | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.91+3684A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394059 | ||||||
| chr11:1394106
|
ATGGAGAT others(6): Show |
A | 1 | a0001c0001t0001g0058 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.91+3755_91+3767del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394106 | |||||
| chr11:1394119
|
CTGGAGAT others(599): Show |
C | 1 | a0002c0002t0016g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.91+3768_91+4373del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394119 | |||||
| chr11:1394169
|
T | C | 1 | a0002c0002t0002g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.91+3794T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394169 | ||||||
| chr11:1394194
|
G | A | 12 | a0001c0001t0001g0044a0001c0001t0001g0313a0001c0001t0001g0317others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.91+3819G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394194 | ||||||
| chr11:1394195
|
G | A | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+3820G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394195 | ||||||
| chr11:1394238
|
ATGGAGAT others(6): Show |
A | 21 | a0001c0001t0001g0044a0001c0001t0001g0312a0001c0001t0001g0313others(18): Show | 21 | HG01346.hp2 HG01433.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.91+3900_91+3912del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394238 | |||||
| chr11:1394288
|
C | T | 10 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(7): Show | 10 | HG01243.hp2 HG02040.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.91+3913C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394288 | ||||||
| chr11:1394290
|
A | C | 10 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(7): Show | 10 | HG01243.hp2 HG02040.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.91+3915A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394290 | ||||||
| chr11:1394300
|
GC | G | 10 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(7): Show | 10 | HG01243.hp2 HG02040.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.91+3929delC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394300 | |||||
| chr11:1394304
|
C | A | 10 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(7): Show | 10 | HG01243.hp2 HG02040.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.91+3929C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394304 | ||||||
| chr11:1394328
|
G | GC | 10 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(7): Show | 10 | HG01243.hp2 HG02040.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.91+3955dupC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394328 | |||||
| chr11:1394331
|
A | C | 10 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(7): Show | 10 | HG01243.hp2 HG02040.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.91+3956A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394331 | ||||||
| chr11:1394331
|
ATGGAGAT others(6): Show |
A | 3 | a0001c0001t0028g0332a0001c0001t0028g0333a0001c0003t0001g0331 | 3 | HG00673.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.91+3980_91+3992del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394331 | |||||
| chr11:1394342
|
T | C | 10 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(7): Show | 10 | HG01243.hp2 HG02040.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.91+3967T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394342 | ||||||
| chr11:1394344
|
C | A | 10 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(7): Show | 10 | HG01243.hp2 HG02040.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.91+3969C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394344 | ||||||
| chr11:1394355
|
TCCTGGAG others(6): Show |
T | 4 | a0001c0001t0045g0040a0001c0003t0014g0037a0002c0002t0015g0027others(1): Show | 4 | HG02257.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+3982_91+3994del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394355 | |||||
| chr11:1394357
|
C | A | 34 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(31): Show | 35 | HG00642.hp2 HG01109.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.91+3982C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394357 | ||||||
| chr11:1394357
|
CTGGAGAT others(6): Show |
C | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91+4006_91+4018del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394357 | |||||
| chr11:1394378
|
G | A | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+4003G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394378 | ||||||
| chr11:1394381
|
C | T | 34 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(31): Show | 35 | HG00642.hp2 HG01109.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.91+4006C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394381 | ||||||
| chr11:1394383
|
A | ATGGAGAT others(6): Show |
4 | a0001c0001t0045g0040a0001c0003t0014g0037a0002c0002t0015g0027others(1): Show | 4 | HG02257.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+4019_91+4031dup others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394383 | |||||
| chr11:1394383
|
A | C | 34 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(31): Show | 35 | HG00642.hp2 HG01109.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.91+4008A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394383 | ||||||
| chr11:1394443
|
T | G | 1 | a0002c0017t0052g0008 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.91+4068T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394443 | ||||||
| chr11:1394460
|
C | T | 4 | a0001c0001t0001g0312a0001c0001t0013g0311a0002c0002t0002g0323others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+4085C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394460 | ||||||
| chr11:1394462
|
A | C | 5 | a0001c0001t0001g0312a0001c0001t0013g0311a0002c0002t0002g0323others(2): Show | 5 | HG02630.hp2 HG02738.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+4087A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394462 | ||||||
| chr11:1394528
|
C | CTGGAGAT others(6): Show |
3 | a0001c0001t0001g0057a0001c0001t0001g0059a0002c0002t0002g0014 | 3 | HG02723.hp1 NA18952.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.91+4164_91+4176dup others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394528 | |||||
| chr11:1394541
|
ATGGAGAT others(6): Show |
A | 6 | a0001c0001t0004g0172a0001c0001t0004g0173a0002c0002t0002g0169others(3): Show | 6 | HG01081.hp1 HG01099.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4190_91+4202del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394541 | |||||
| chr11:1394567
|
CTGGAGAT others(6): Show |
C | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+4203_91+4215del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394567 | |||||
| chr11:1394579
|
CATGGAGA others(5): Show |
C | 2 | a0001c0001t0001g0057a0001c0001t0001g0059 | 2 | NA18952.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.91+4205_91+4216del others(12): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394579 | ||||||
| chr11:1394580
|
ATGGAGAT others(6): Show |
A | 2 | a0002c0002t0005g0258a0002c0002t0005g0259 | 2 | HG02027.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.91+4216_91+4228del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394580 | |||||
| chr11:1394606
|
A | ATGGAGAT others(6): Show |
1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+4255_91+4267dup others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394606 | |||||
| chr11:1394656
|
T | TC | 14 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(11): Show | 14 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.91+4283dupC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394656 | |||||
| chr11:1394660
|
G | A | 1 | a0002c0002t0002g0060 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.91+4285G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394660 | ||||||
| chr11:1394669
|
C | T | 134 | a0001c0001t0003g0002a0001c0001t0003g0045a0001c0001t0003g0193others(131): Show | 139 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.91+4294C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394669 | ||||||
| chr11:1394670
|
CCCTGGAG others(6): Show |
C | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0024g0292 | 3 | HG01943.hp2 HG02145.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.91+4324_91+4336del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394670 | |||||
| chr11:1394683
|
T | TCCTGGAG others(7): Show |
6 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+4320_91+4321ins others(14): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394683 | |||||
| chr11:1394709
|
TCCCTGGA others(46): Show |
T | 1 | a0002c0002t0005g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.91+4389_91+4441del others(53): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394709 | |||||
| chr11:1394710
|
C | G | 3 | a0002c0002t0002g0164a0002c0002t0002g0166a0002c0002t0050g0165 | 3 | HG00544.hp2 NA18612.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.91+4335C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394710 | ||||||
| chr11:1394710
|
CCCTGGAG others(269): Show |
C | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0004g0190 | 3 | HG01123.hp2 HG01891.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.91+4350_91+4625del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394710 | |||||
| chr11:1394725
|
A | ATGGAGAT others(6): Show |
2 | a0001c0001t0006g0251a0001c0001t0067g0252 | 2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.91+4374_91+4386dup others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394725 | |||||
| chr11:1394761
|
GC | G | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+4390delC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394761 | |||||
| chr11:1394765
|
C | A | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+4390C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394765 | ||||||
| chr11:1394776
|
C | T | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+4401C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394776 | ||||||
| chr11:1394778
|
A | C | 13 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0018g0334others(10): Show | 13 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+4403A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394778 | ||||||
| chr11:1394804
|
C | CTGGAGAT others(6): Show |
1 | a0001c0001t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.91+4440_91+4452dup others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394804 | |||||
| chr11:1394817
|
ATGGAGAT others(6): Show |
A | 3 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | HG02698.hp1 HG03492.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.91+4466_91+4478del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394817 | |||||
| chr11:1394817
|
ATGGAGAT others(98): Show |
A | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+4519_91+4623del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394817 | |||||
| chr11:1394853
|
GC | G | 9 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(6): Show | 9 | HG01243.hp1 HG01433.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+4482delC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394853 | |||||
| chr11:1394855
|
C | T | 7 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0052others(4): Show | 7 | HG01243.hp1 HG01943.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+4480C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394855 | ||||||
| chr11:1394857
|
C | A | 1 | a0001c0001t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.91+4482C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394857 | ||||||
| chr11:1394865
|
G | A | 1 | a0001c0001t0003g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.91+4490G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394865 | ||||||
| chr11:1394868
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.91+4493C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394868 | ||||||
| chr11:1394870
|
A | ATGGAGAT others(6): Show |
7 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0052others(4): Show | 7 | HG01243.hp1 HG01943.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+4519_91+4531dup others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394870 | |||||
| chr11:1394870
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.91+4495A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394870 | ||||||
| chr11:1394878
|
G | A | 20 | a0001c0001t0001g0186a0001c0001t0004g0172a0001c0001t0004g0173others(17): Show | 20 | HG01069.hp1 HG01081.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.91+4503G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394878 | ||||||
| chr11:1394883
|
CTGGAGAT others(85): Show |
C | 1 | a0002c0002t0016g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.91+4534_91+4625del others(92): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394883 | |||||
| chr11:1394889
|
A | G | 62 | a0001c0001t0003g0193a0001c0001t0003g0199a0001c0001t0003g0219others(59): Show | 64 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.91+4514A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394889 | ||||||
| chr11:1394909
|
ATGGAGAT others(6): Show |
A | 1 | a0001c0001t0009g0120 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.91+4571_91+4583del others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1394909 | |||||
| chr11:1394947
|
C | T | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.91+4572C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394947 | ||||||
| chr11:1394968
|
A | T | 2 | a0002c0002t0005g0250a0002c0002t0008g0167 | 2 | HG03017.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.91+4593A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1394968 | ||||||
| chr11:1395031
|
G | A | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91+4656G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395031 | ||||||
| chr11:1395095
|
C | T | 1 | a0002c0002t0030g0174 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.91+4720C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395095 | ||||||
| chr11:1395112
|
G | A | 9 | a0001c0001t0001g0044a0001c0001t0001g0313a0001c0001t0001g0317others(6): Show | 9 | HG01433.hp1 HG01943.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+4737G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395112 | ||||||
| chr11:1395217
|
C | T | 1 | a0001c0001t0011g0310 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.91+4842C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395217 | ||||||
| chr11:1395256
|
C | T | 4 | a0001c0001t0004g0172a0001c0001t0004g0173a0002c0002t0030g0171others(1): Show | 4 | HG01081.hp1 HG02683.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+4881C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395256 | ||||||
| chr11:1395275
|
G | A | 4 | a0001c0001t0001g0312a0001c0001t0013g0311a0001c0003t0004g0290others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+4900G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395275 | ||||||
| chr11:1395298
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG01943.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.91+4923C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395298 | ||||||
| chr11:1395314
|
C | T | 9 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(6): Show | 9 | HG01243.hp1 HG01943.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.91+4939C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395314 | ||||||
| chr11:1395347
|
C | T | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+4972C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395347 | ||||||
| chr11:1395368
|
C | T | 1 | a0002c0002t0008g0116 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.91+4993C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395368 | ||||||
| chr11:1395392
|
C | T | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 44 | HG00642.hp2 HG01109.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.91+5017C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395392 | ||||||
| chr11:1395426
|
C | T | 1 | a0002c0002t0008g0162 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.91+5051C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395426 | ||||||
| chr11:1395574
|
C | T | 1 | a0002c0002t0002g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.91+5199C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395574 | ||||||
| chr11:1395578
|
A | G | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0002c0002t0017g0353 | 3 | HG00408.hp1 HG00544.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.91+5203A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395578 | ||||||
| chr11:1395692
|
C | T | 1 | a0001c0001t0006g0248 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.91+5317C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395692 | ||||||
| chr11:1395709
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0004g0051 | 2 | HG01243.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.91+5334C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395709 | ||||||
| chr11:1395758
|
C | T | 4 | a0001c0001t0006g0247a0001c0001t0006g0251a0001c0001t0011g0310others(1): Show | 4 | HG00140.hp1 HG01175.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+5383C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395758 | ||||||
| chr11:1395767
|
C | T | 1 | a0003c0014t0002g0319 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.91+5392C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395767 | ||||||
| chr11:1395845
|
G | T | 1 | a0002c0002t0010g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.91+5470G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395845 | ||||||
| chr11:1395992
|
G | T | 1 | a0002c0011t0002g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.91+5617G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1395992 | ||||||
| chr11:1396055
|
C | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0003g0199 | 3 | HG02055.hp2 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.91+5680C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396055 | ||||||
| chr11:1396166
|
G | GCGTCCCC others(65): Show |
2 | a0001c0001t0003g0280a0001c0001t0011g0307 | 2 | HG04184.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.91+5800_91+5871dup others(72): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396166 | |||||
| chr11:1396166
|
G | GCGTCCCC others(137): Show |
1 | a0002c0002t0008g0162 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(144): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396166 | |||||
| chr11:1396166
|
G | GCGTCCCC others(173): Show |
1 | a0002c0002t0008g0157 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(180): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396166 | |||||
| chr11:1396166
|
G | GCGTCCCC others(137): Show |
1 | a0002c0002t0002g0098 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.91+5907_91+5908ins others(144): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396166 | |||||
| chr11:1396168
|
G | A | 14 | a0001c0001t0004g0175a0001c0001t0004g0177a0001c0001t0021g0206others(11): Show | 14 | HG00738.hp1 HG01081.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.91+5793G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396168 | ||||||
| chr11:1396172
|
C | T | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+5797C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396172 | ||||||
| chr11:1396175
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.91+5800G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396175 | ||||||
| chr11:1396175
|
G | GCTCCTCG others(29): Show |
1 | a0002c0002t0005g0211 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.91+5806_91+5841dup others(36): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396175 | |||||
| chr11:1396175
|
G | GCTCCTGG others(29): Show |
5 | a0001c0001t0001g0107a0001c0001t0042g0160a0002c0002t0002g0318others(2): Show | 5 | HG00280.hp1 HG00735.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+5805_91+5806ins others(36): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396175 | |||||
| chr11:1396175
|
G | GCTCCTGG others(65): Show |
1 | a0001c0001t0004g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.91+5805_91+5806ins others(72): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396175 | |||||
| chr11:1396175
|
G | GCTCCTGG others(101): Show |
2 | a0001c0001t0001g0053a0002c0002t0002g0031 | 2 | HG01943.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.91+5805_91+5806ins others(108): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396175 | |||||
| chr11:1396175
|
G | GCTCCTGG others(137): Show |
2 | a0001c0001t0001g0108a0001c0001t0021g0242 | 2 | HG02300.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.91+5805_91+5806ins others(144): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396175 | |||||
| chr11:1396175
|
G | GCTCCTGG others(173): Show |
3 | a0001c0001t0043g0050a0001c0001t0048g0342a0001c0001t0068g0243 | 3 | HG01255.hp2 HG02647.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.91+5805_91+5806ins others(180): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396175 | |||||
| chr11:1396175
|
G | GCTCCTGG others(245): Show |
2 | a0001c0001t0028g0332a0001c0001t0028g0333 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.91+5805_91+5806ins others(252): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396175 | |||||
| chr11:1396175
|
G | GCTCCTGG others(317): Show |
1 | a0001c0001t0001g0112 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.91+5805_91+5806ins others(324): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396175 | |||||
| chr11:1396175
|
G | GCTCCTGG others(317): Show |
1 | a0001c0001t0001g0191 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.91+5805_91+5806ins others(324): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396175 | |||||
| chr11:1396175
|
GCTCCTCG others(29): Show |
G | 4 | a0001c0001t0001g0105a0001c0001t0003g0241a0001c0001t0004g0106others(1): Show | 4 | HG01256.hp1 HG01257.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+5806_91+5841del others(36): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396175 | |||||
| chr11:1396175
|
GCTCCTCG others(65): Show |
G | 1 | a0001c0001t0001g0104 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.91+5806_91+5877del others(72): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396175 | |||||
| chr11:1396181
|
C | CGTCCCTC others(29): Show |
1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.91+5809_91+5810ins others(36): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396181 | |||||
| chr11:1396181
|
C | CGTCCCTC others(65): Show |
1 | a0001c0001t0001g0048 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.91+5809_91+5810ins others(72): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396181 | |||||
| chr11:1396181
|
C | CGTCTCTC others(65): Show |
1 | a0002c0002t0002g0164 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.91+5841_91+5842ins others(72): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396181 | |||||
| chr11:1396181
|
C | CGTCTCTC others(137): Show |
1 | a0001c0001t0045g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(144): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396181 | |||||
| chr11:1396181
|
C | G | 26 | a0001c0001t0001g0053a0001c0001t0001g0107a0001c0001t0001g0108others(23): Show | 26 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.91+5806C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396181 | ||||||
| chr11:1396181
|
CGTCTCTC others(29): Show |
C | 1 | a0001c0006t0001g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.91+5810_91+5845del others(36): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396181 | |||||
| chr11:1396185
|
T | C | 28 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0048others(25): Show | 28 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.91+5810T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396185 | ||||||
| chr11:1396185
|
T | TCTCTTCC others(65): Show |
1 | a0001c0001t0018g0334 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.91+5841_91+5842ins others(72): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(101): Show |
1 | a0001c0001t0001g0111 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.91+5841_91+5842ins others(108): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(29): Show |
56 | a0001c0001t0001g0057a0001c0001t0001g0076a0001c0001t0001g0082others(53): Show | 56 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.91+5893_91+5928dup others(36): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(137): Show |
1 | a0001c0001t0001g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.91+5877_91+5878ins others(144): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(65): Show |
15 | a0001c0001t0001g0168a0001c0001t0003g0002a0001c0001t0003g0227others(12): Show | 16 | HG00558.hp2 HG01175.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.91+5857_91+5928dup others(72): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(100): Show |
1 | a0001c0003t0026g0054 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.91+5897_91+5898ins others(107): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(101): Show |
14 | a0001c0001t0001g0052a0001c0001t0001g0150a0001c0001t0003g0196others(11): Show | 14 | HG00609.hp1 HG01515.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.91+5821_91+5928dup others(108): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(137): Show |
13 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0192others(10): Show | 13 | HG00408.hp2 HG01099.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+5928_91+5929ins others(144): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(173): Show |
8 | a0001c0001t0001g0154a0001c0001t0003g0230a0001c0001t0003g0287others(5): Show | 8 | HG00621.hp2 HG01891.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.91+5928_91+5929ins others(180): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(209): Show |
2 | a0001c0001t0003g0194a0002c0002t0002g0155 | 2 | HG03540.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.91+5928_91+5929ins others(216): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(245): Show |
1 | a0002c0002t0002g0166 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(252): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(281): Show |
1 | a0001c0001t0004g0185 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(288): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(317): Show |
1 | a0002c0002t0020g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(324): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(389): Show |
1 | a0002c0002t0033g0279 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(396): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(425): Show |
3 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0006g0248 | 3 | HG02683.hp2 HG03017.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.91+5928_91+5929ins others(432): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(173): Show |
1 | a0001c0001t0001g0097 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(180): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(137): Show |
1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.91+5917_91+5918ins others(144): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(209): Show |
1 | a0001c0001t0001g0029 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.91+5907_91+5908ins others(216): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(101): Show |
2 | a0001c0001t0001g0030a0001c0001t0001g0049 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.91+5881_91+5882ins others(108): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(173): Show |
1 | a0002c0002t0002g0103 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.91+5871_91+5872ins others(180): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
T | TCTCTTCC others(137): Show |
1 | a0001c0001t0001g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.91+5852_91+5853ins others(144): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
TCTCTTCC others(29): Show |
T | 61 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0044others(58): Show | 62 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.91+5893_91+5928del others(36): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396185
|
TCTCTTCC others(65): Show |
T | 29 | a0001c0001t0001g0058a0001c0001t0003g0200a0001c0001t0003g0201others(26): Show | 32 | HG00323.hp1 HG01109.hp2 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.91+5857_91+5928del others(72): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396185 | |||||
| chr11:1396211
|
A | ACTCCTGG others(65): Show |
1 | a0001c0001t0004g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.91+5871_91+5872ins others(72): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396211 | |||||
| chr11:1396211
|
A | G | 2 | a0002c0002t0005g0281a0002c0002t0007g0308 | 2 | HG01993.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.91+5836A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396211 | ||||||
| chr11:1396217
|
G | C | 4 | a0002c0002t0005g0211a0002c0002t0005g0260a0002c0002t0005g0281others(1): Show | 4 | HG01346.hp1 HG01993.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+5842G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396217 | ||||||
| chr11:1396221
|
C | CCTCTTCC others(353): Show |
1 | a0001c0001t0076g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(360): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(209): Show |
1 | a0002c0002t0007g0309 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(216): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(245): Show |
1 | a0002c0002t0069g0231 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(252): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(209): Show |
2 | a0001c0001t0003g0232a0002c0002t0016g0207 | 2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.91+5928_91+5929ins others(216): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(101): Show |
8 | a0001c0004t0001g0091a0001c0004t0001g0093a0001c0004t0001g0094others(5): Show | 8 | HG02155.hp1 HG02165.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+5928_91+5929ins others(108): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(245): Show |
1 | a0001c0004t0001g0096 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(252): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(173): Show |
1 | a0002c0002t0016g0208 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(180): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(65): Show |
4 | a0001c0001t0001g0186a0001c0001t0003g0234a0001c0001t0009g0187others(1): Show | 4 | HG02818.hp2 NA18964.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+5907_91+5908ins others(72): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(245): Show |
1 | a0002c0002t0007g0304 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.91+5907_91+5908ins others(252): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(209): Show |
1 | a0002c0002t0017g0305 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.91+5907_91+5908ins others(216): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(101): Show |
3 | a0001c0001t0003g0199a0001c0001t0003g0235a0001c0001t0003g0236 | 3 | HG02622.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.91+5907_91+5908ins others(108): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(245): Show |
1 | a0001c0001t0003g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.91+5907_91+5908ins others(252): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(137): Show |
3 | a0001c0001t0003g0238a0001c0001t0032g0209a0001c0001t0070g0210 | 3 | HG01070.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.91+5907_91+5908ins others(144): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(29): Show |
8 | a0001c0001t0001g0099a0001c0001t0001g0102a0001c0001t0003g0288others(5): Show | 8 | HG01167.hp1 HG02074.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+5871_91+5872ins others(36): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | CCTCTTCC others(65): Show |
1 | a0002c0002t0016g0240 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.91+5871_91+5872ins others(72): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396221 | |||||
| chr11:1396221
|
C | T | 4 | a0002c0002t0005g0211a0002c0002t0005g0260a0002c0002t0005g0281others(1): Show | 4 | HG01346.hp1 HG01993.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+5846C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396221 | ||||||
| chr11:1396232
|
C | CCACCCAC others(29): Show |
2 | a0001c0003t0001g0335a0001c0003t0001g0336 | 2 | NA19080.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.91+5892_91+5893ins others(36): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396232 | |||||
| chr11:1396232
|
C | CCACCCAC others(65): Show |
1 | a0001c0003t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.91+5860_91+5931dup others(72): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396232 | |||||
| chr11:1396235
|
C | CCCACGTC others(101): Show |
1 | a0002c0002t0038g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(108): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396235 | |||||
| chr11:1396247
|
A | ACTCCTCG others(29): Show |
1 | a0001c0001t0060g0163 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.91+5877_91+5878ins others(36): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396247 | |||||
| chr11:1396247
|
A | ACTCCTGG others(29): Show |
1 | a0001c0001t0003g0239 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.91+5907_91+5908ins others(36): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396247 | |||||
| chr11:1396247
|
A | G | 2 | a0001c0001t0004g0188a0002c0002t0033g0286 | 2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.91+5872A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396247 | ||||||
| chr11:1396253
|
G | C | 1 | a0001c0001t0060g0163 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.91+5878G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396253 | ||||||
| chr11:1396257
|
C | CCTCTTCC others(209): Show |
1 | a0001c0001t0004g0173 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.91+5928_91+5929ins others(216): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396257 | |||||
| chr11:1396257
|
C | T | 1 | a0001c0001t0060g0163 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.91+5882C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396257 | ||||||
| chr11:1396271
|
C | CCCACGTC others(29): Show |
1 | a0001c0001t0063g0253 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+5899_91+5934dup others(36): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1396271 | |||||
| chr11:1396372
|
G | A | 1 | a0001c0001t0076g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.91+5997G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396372 | ||||||
| chr11:1396415
|
C | T | 9 | a0001c0001t0001g0150a0001c0003t0014g0036a0001c0003t0014g0037others(6): Show | 9 | HG00609.hp1 HG01433.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.91+6040C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396415 | ||||||
| chr11:1396467
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+6092C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396467 | ||||||
| chr11:1396476
|
G | A | 1 | a0001c0001t0003g0268 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.91+6101G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396476 | ||||||
| chr11:1396603
|
G | A | 1 | a0002c0002t0020g0148 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.91+6228G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396603 | ||||||
| chr11:1396633
|
G | A | 1 | a0002c0002t0002g0103 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.91+6258G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396633 | ||||||
| chr11:1396668
|
C | T | 1 | a0001c0001t0021g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.91+6293C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396668 | ||||||
| chr11:1396745
|
G | A | 1 | a0001c0001t0014g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.91+6370G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396745 | ||||||
| chr11:1396784
|
G | A | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91+6409G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396784 | ||||||
| chr11:1396800
|
C | T | 2 | a0001c0001t0004g0106a0001c0001t0006g0282 | 2 | HG01123.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.91+6425C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396800 | ||||||
| chr11:1396997
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.91+6622G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1396997 | ||||||
| chr11:1397087
|
G | A | 3 | a0002c0002t0002g0015a0002c0002t0033g0286a0002c0002t0066g0285 | 3 | HG02738.hp2 HG03453.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.91+6712G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397087 | ||||||
| chr11:1397122
|
G | A | 1 | a0001c0001t0004g0185 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.91+6747G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397122 | ||||||
| chr11:1397198
|
G | C | 1 | a0002c0002t0005g0264 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.91+6823G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397198 | ||||||
| chr11:1397220
|
A | G | 105 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(102): Show | 107 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.91+6845A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397220 | ||||||
| chr11:1397232
|
C | T | 2 | a0001c0001t0001g0343a0001c0001t0047g0340 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.91+6857C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397232 | ||||||
| chr11:1397247
|
T | C | 1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.91+6872T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397247 | ||||||
| chr11:1397351
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+6976G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397351 | ||||||
| chr11:1397376
|
A | T | 1 | a0001c0003t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.91+7001A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397376 | ||||||
| chr11:1397378
|
C | T | 3 | a0001c0001t0001g0312a0002c0008t0002g0326a0002c0008t0005g0278 | 3 | HG01884.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.91+7003C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397378 | ||||||
| chr11:1397450
|
A | T | 1 | a0001c0001t0001g0102 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.91+7075A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397450 | ||||||
| chr11:1397526
|
C | T | 1 | a0001c0001t0009g0128 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.91+7151C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397526 | ||||||
| chr11:1397543
|
G | A | 1 | a0001c0001t0062g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.91+7168G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397543 | ||||||
| chr11:1397647
|
A | C | 47 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(44): Show | 48 | HG00323.hp2 HG00558.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.91+7272A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397647 | ||||||
| chr11:1397915
|
A | G | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 80 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.91+7540A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397915 | ||||||
| chr11:1397986
|
G | A | 1 | a0002c0017t0052g0008 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.91+7611G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1397986 | ||||||
| chr11:1398031
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.91+7656G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398031 | ||||||
| chr11:1398054
|
A | C | 257 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(254): Show | 260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.91+7679A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398054 | ||||||
| chr11:1398085
|
C | CG | 10 | a0001c0001t0001g0044a0001c0001t0001g0127a0001c0001t0001g0141others(7): Show | 10 | HG00140.hp2 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+7715dupG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1398085 | |||||
| chr11:1398119
|
C | G | 201 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(198): Show | 203 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.91+7744C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398119 | ||||||
| chr11:1398119
|
C | T | 50 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0339others(47): Show | 51 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.91+7744C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398119 | ||||||
| chr11:1398181
|
A | G | 128 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0057others(125): Show | 130 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.91+7806A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398181 | ||||||
| chr11:1398207
|
A | G | 206 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(203): Show | 208 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.91+7832A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398207 | ||||||
| chr11:1398259
|
C | T | 1 | a0002c0002t0005g0258 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.91+7884C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398259 | ||||||
| chr11:1398268
|
G | A | 114 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0049others(111): Show | 115 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.91+7893G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398268 | ||||||
| chr11:1398317
|
G | A | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.91+7942G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398317 | ||||||
| chr11:1398381
|
C | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0023others(41): Show | 45 | HG00323.hp2 HG00558.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.91+8006C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398381 | ||||||
| chr11:1398558
|
G | A | 1 | a0002c0002t0051g0077 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.91+8183G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398558 | ||||||
| chr11:1398589
|
A | C | 1 | a0002c0002t0002g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.91+8214A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398589 | ||||||
| chr11:1398714
|
C | T | 96 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(93): Show | 97 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.91+8339C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398714 | ||||||
| chr11:1398784
|
G | A | 5 | a0001c0001t0031g0012a0001c0001t0032g0195a0001c0001t0032g0209others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+8409G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398784 | ||||||
| chr11:1398882
|
G | C | 1 | a0001c0001t0004g0172 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.91+8507G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398882 | ||||||
| chr11:1398939
|
C | T | 1 | a0001c0001t0011g0352 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.91+8564C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398939 | ||||||
| chr11:1398947
|
C | A | 1 | a0002c0002t0005g0269 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.91+8572C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398947 | ||||||
| chr11:1398947
|
C | T | 1 | a0002c0002t0002g0155 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.91+8572C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398947 | ||||||
| chr11:1398968
|
G | A | 25 | a0001c0001t0001g0046a0001c0001t0001g0113a0001c0001t0001g0154others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.91+8593G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1398968 | ||||||
| chr11:1399049
|
C | T | 58 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(55): Show | 58 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.91+8674C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1399049 | ||||||
| chr11:1399070
|
C | T | 6 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(3): Show | 6 | HG01192.hp1 HG01952.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+8695C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1399070 | ||||||
| chr11:1399188
|
G | GC | 10 | a0001c0001t0001g0044a0001c0001t0001g0127a0001c0001t0001g0141others(7): Show | 10 | HG00140.hp2 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+8819dupC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1399188 | |||||
| chr11:1399192
|
C | A | 2 | a0001c0001t0006g0215a0001c0001t0074g0213 | 2 | HG01261.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.91+8817C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1399192 | ||||||
| chr11:1399311
|
A | AGG | 23 | a0001c0001t0001g0113a0001c0001t0001g0154a0001c0001t0001g0189others(20): Show | 23 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.91+8940_91+8941dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1399311 | |||||
| chr11:1399311
|
A | G | 10 | a0001c0001t0001g0044a0001c0001t0001g0127a0001c0001t0001g0141others(7): Show | 10 | HG00140.hp2 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+8936A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1399311 | ||||||
| chr11:1399327
|
T | C | 252 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(249): Show | 255 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.91+8952T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1399327 | ||||||
| chr11:1399419
|
C | T | 1 | a0001c0001t0011g0310 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.91+9044C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1399419 | ||||||
| chr11:1399634
|
G | T | 1 | a0001c0001t0004g0175 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.91+9259G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1399634 | ||||||
| chr11:1399839
|
A | G | 205 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.91+9464A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1399839 | ||||||
| chr11:1399908
|
T | TGGG | 257 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(254): Show | 260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.91+9533_91+9534ins others(3): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1399908 | ||||||
| chr11:1399968
|
C | T | 35 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0168others(32): Show | 36 | HG00323.hp2 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+9593C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1399968 | ||||||
| chr11:1400167
|
C | T | 2 | a0001c0001t0028g0332a0001c0001t0028g0333 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.91+9792C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1400167 | ||||||
| chr11:1400259
|
A | G | 259 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(256): Show | 262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.91+9884A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1400259 | ||||||
| chr11:1400437
|
C | T | 1 | a0001c0003t0001g0135 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.91+10062C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1400437 | ||||||
| chr11:1400473
|
A | G | 205 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.91+10098A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1400473 | ||||||
| chr11:1400486
|
T | C | 152 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0057others(149): Show | 153 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.91+10111T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1400486 | ||||||
| chr11:1400577
|
G | A | 1 | a0001c0001t0067g0252 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.91+10202G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1400577 | ||||||
| chr11:1400589
|
A | G | 52 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(49): Show | 53 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.91+10214A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1400589 | ||||||
| chr11:1400657
|
CG | C | 25 | a0001c0001t0001g0046a0001c0001t0001g0113a0001c0001t0001g0154others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.91+10288delG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1400657 | |||||
| chr11:1400749
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.91+10374G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1400749 | ||||||
| chr11:1400773
|
C | T | 1 | a0001c0001t0045g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.91+10398C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1400773 | ||||||
| chr11:1400778
|
C | T | 2 | a0002c0007t0010g0244a0002c0007t0010g0245 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.91+10403C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1400778 | ||||||
| chr11:1400917
|
C | T | 38 | a0001c0001t0001g0049a0001c0001t0001g0072a0001c0001t0001g0087others(35): Show | 39 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.91+10542C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1400917 | ||||||
| chr11:1400990
|
A | G | 48 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 49 | HG00323.hp2 HG00558.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.91+10615A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1400990 | ||||||
| chr11:1401053
|
A | G | 8 | a0001c0001t0001g0168a0001c0001t0001g0186a0001c0001t0001g0317others(5): Show | 8 | HG00558.hp1 HG02129.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+10678A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401053 | ||||||
| chr11:1401157
|
C | T | 1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.91+10782C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401157 | ||||||
| chr11:1401163
|
C | G | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+10788C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401163 | ||||||
| chr11:1401284
|
C | G | 1 | a0002c0017t0052g0008 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.91+10909C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401284 | ||||||
| chr11:1401329
|
C | T | 2 | a0001c0001t0003g0227a0001c0001t0003g0241 | 2 | HG01257.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.91+10954C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401329 | ||||||
| chr11:1401496
|
C | T | 152 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0057others(149): Show | 153 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.91+11121C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401496 | ||||||
| chr11:1401564
|
T | C | 152 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0057others(149): Show | 153 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.91+11189T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401564 | ||||||
| chr11:1401569
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.91+11194C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401569 | ||||||
| chr11:1401590
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.91+11215G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401590 | ||||||
| chr11:1401608
|
C | T | 26 | a0001c0001t0001g0046a0001c0001t0001g0113a0001c0001t0001g0154others(23): Show | 26 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.91+11233C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401608 | ||||||
| chr11:1401663
|
CT | C | 3 | a0001c0001t0001g0048a0001c0001t0043g0050a0002c0002t0002g0015 | 3 | HG02647.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.91+11289delT | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401663 | ||||||
| chr11:1401673
|
G | A | 1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.91+11298G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401673 | ||||||
| chr11:1401703
|
A | G | 1 | a0001c0001t0003g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.91+11328A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401703 | ||||||
| chr11:1401706
|
A | T | 3 | a0001c0001t0009g0153a0002c0002t0008g0151a0005c0010t0002g0085 | 3 | HG00408.hp2 NA18612.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.91+11331A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401706 | ||||||
| chr11:1401755
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+11380G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401755 | ||||||
| chr11:1401762
|
G | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0003g0002others(2): Show | 6 | HG02572.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+11387G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401762 | ||||||
| chr11:1401818
|
C | T | 1 | a0007c0013t0004g0065 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.91+11443C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401818 | ||||||
| chr11:1401946
|
C | T | 151 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0057others(148): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.91+11571C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1401946 | ||||||
| chr11:1402042
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0107 | 2 | HG00280.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.91+11667C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402042 | ||||||
| chr11:1402060
|
G | A | 1 | a0001c0001t0004g0090 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.91+11685G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402060 | ||||||
| chr11:1402105
|
C | T | 1 | a0001c0003t0001g0135 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.91+11730C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402105 | ||||||
| chr11:1402183
|
C | T | 1 | a0002c0002t0008g0167 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.91+11808C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402183 | ||||||
| chr11:1402205
|
G | A | 6 | a0001c0001t0001g0049a0001c0001t0003g0200a0001c0001t0003g0201others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+11830G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402205 | ||||||
| chr11:1402221
|
C | T | 14 | a0001c0001t0001g0044a0001c0001t0001g0192a0001c0001t0001g0312others(11): Show | 14 | HG00642.hp1 HG01070.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.91+11846C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402221 | ||||||
| chr11:1402232
|
A | C | 1 | a0001c0001t0006g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.91+11857A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402232 | ||||||
| chr11:1402389
|
A | G | 25 | a0001c0001t0001g0046a0001c0001t0001g0113a0001c0001t0001g0154others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.91+12014A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402389 | ||||||
| chr11:1402487
|
T | C | 205 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.91+12112T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402487 | ||||||
| chr11:1402495
|
G | A | 126 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.91+12120G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402495 | ||||||
| chr11:1402507
|
G | T | 1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.91+12132G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402507 | ||||||
| chr11:1402540
|
A | G | 151 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0057others(148): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.91+12165A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402540 | ||||||
| chr11:1402629
|
AG | A | 49 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(46): Show | 50 | HG00323.hp2 HG00558.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.91+12256delG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1402629 | |||||
| chr11:1402728
|
C | A | 1 | a0001c0001t0001g0343 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.91+12353C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402728 | ||||||
| chr11:1402754
|
C | T | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.91+12379C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402754 | ||||||
| chr11:1402779
|
G | A | 2 | a0001c0001t0006g0215a0001c0001t0074g0213 | 2 | HG01261.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.91+12404G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402779 | ||||||
| chr11:1402832
|
C | G | 25 | a0001c0001t0001g0046a0001c0001t0001g0113a0001c0001t0001g0154others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.91+12457C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402832 | ||||||
| chr11:1402851
|
G | C | 25 | a0001c0001t0001g0046a0001c0001t0001g0113a0001c0001t0001g0154others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.91+12476G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402851 | ||||||
| chr11:1402932
|
G | C | 1 | a0001c0001t0001g0111 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.91+12557G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402932 | ||||||
| chr11:1402950
|
G | A | 1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.91+12575G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1402950 | ||||||
| chr11:1403037
|
A | G | 131 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0057others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.91+12662A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403037 | ||||||
| chr11:1403044
|
G | A | 131 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0057others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.91+12669G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403044 | ||||||
| chr11:1403055
|
G | A | 1 | a0003c0014t0002g0319 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.91+12680G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403055 | ||||||
| chr11:1403057
|
G | T | 3 | a0001c0001t0009g0068a0001c0001t0009g0100a0001c0001t0009g0101 | 3 | NA18966.hp1 NA18975.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.91+12682G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403057 | ||||||
| chr11:1403076
|
G | A | 105 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(102): Show | 106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.91+12701G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403076 | ||||||
| chr11:1403085
|
C | T | 1 | a0001c0001t0014g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.91+12710C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403085 | ||||||
| chr11:1403112
|
T | C | 205 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.91+12737T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403112 | ||||||
| chr11:1403170
|
T | C | 157 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(154): Show | 158 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.91+12795T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403170 | ||||||
| chr11:1403409
|
TGCTGGGG others(5): Show |
T | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+13039_91+13050d others(14): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1403409 | |||||
| chr11:1403521
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0004g0190 | 3 | HG01123.hp2 HG01891.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.91+13146G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403521 | ||||||
| chr11:1403531
|
G | A | 1 | a0001c0001t0075g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+13156G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403531 | ||||||
| chr11:1403542
|
A | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+13167A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403542 | ||||||
| chr11:1403616
|
C | T | 24 | a0001c0001t0001g0168a0001c0001t0001g0186a0001c0001t0001g0317others(21): Show | 24 | HG00323.hp2 HG00558.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.91+13241C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403616 | ||||||
| chr11:1403700
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+13325C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403700 | ||||||
| chr11:1403784
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+13409G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403784 | ||||||
| chr11:1403951
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.91+13576C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403951 | ||||||
| chr11:1403995
|
C | G | 1 | a0001c0001t0001g0048 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.91+13620C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1403995 | ||||||
| chr11:1404007
|
C | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(46): Show | 50 | HG00323.hp2 HG00558.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.91+13632C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404007 | ||||||
| chr11:1404104
|
C | T | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91+13729C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404104 | ||||||
| chr11:1404207
|
C | T | 1 | a0005c0010t0002g0085 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.91+13832C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404207 | ||||||
| chr11:1404233
|
C | T | 25 | a0001c0001t0001g0046a0001c0001t0001g0113a0001c0001t0001g0154others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.91+13858C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404233 | ||||||
| chr11:1404344
|
C | G | 1 | a0001c0001t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.91+13969C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404344 | ||||||
| chr11:1404375
|
A | G | 257 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(254): Show | 260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.91+14000A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404375 | ||||||
| chr11:1404415
|
A | G | 105 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(102): Show | 106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.91+14040A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404415 | ||||||
| chr11:1404432
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.91+14057C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404432 | ||||||
| chr11:1404506
|
G | A | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.91+14131G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404506 | ||||||
| chr11:1404603
|
G | A | 3 | a0001c0001t0004g0314a0001c0001t0004g0316a0002c0002t0002g0318 | 3 | HG01943.hp1 HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.91+14228G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404603 | ||||||
| chr11:1404680
|
C | T | 169 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(166): Show | 171 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.91+14305C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404680 | ||||||
| chr11:1404753
|
C | T | 1 | a0002c0002t0016g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.91+14378C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404753 | ||||||
| chr11:1404772
|
A | G | 27 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.91+14397A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404772 | ||||||
| chr11:1404848
|
G | C | 23 | a0001c0001t0001g0113a0001c0001t0001g0154a0001c0001t0001g0189others(20): Show | 23 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.91+14473G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404848 | ||||||
| chr11:1404891
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+14516C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404891 | ||||||
| chr11:1404957
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+14582A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1404957 | ||||||
| chr11:1405016
|
T | TGGCTCTC others(47): Show |
1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+14681_91+14682i others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1405016 | |||||
| chr11:1405016
|
T | TGGCTCTC others(47): Show |
252 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(249): Show | 255 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.91+14656_91+14709d others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1405016 | |||||
| chr11:1405016
|
T | TGGCTCTC others(47): Show |
2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.91+14675_91+14676i others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1405016 | |||||
| chr11:1405018
|
G | GCTCTCTG others(47): Show |
95 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0099others(92): Show | 98 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.91+14696_91+14697i others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1405018 | |||||
| chr11:1405315
|
G | A | 27 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0003g0193others(24): Show | 27 | HG00280.hp2 HG01081.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.91+14940G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1405315 | ||||||
| chr11:1405323
|
ATGTGTGT others(22): Show |
A | 1 | a0002c0002t0007g0350 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.91+14959_91+14987d others(31): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1405323 | |||||
| chr11:1405476
|
G | A | 1 | a0002c0002t0002g0103 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.91+15101G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1405476 | ||||||
| chr11:1405582
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+15207G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1405582 | ||||||
| chr11:1405604
|
G | A | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 73 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.91+15229G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1405604 | ||||||
| chr11:1405697
|
G | A | 1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.91+15322G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1405697 | ||||||
| chr11:1405805
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0107 | 2 | HG00280.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.91+15430G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1405805 | ||||||
| chr11:1405845
|
C | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+15470C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1405845 | ||||||
| chr11:1405906
|
C | T | 1 | a0001c0001t0075g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+15531C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1405906 | ||||||
| chr11:1405929
|
G | A | 4 | a0001c0001t0003g0230a0001c0001t0003g0234a0001c0001t0003g0238others(1): Show | 4 | HG01070.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+15554G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1405929 | ||||||
| chr11:1406074
|
C | G | 1 | a0001c0001t0006g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.91+15699C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406074 | ||||||
| chr11:1406241
|
C | CGGTGGA | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+15866_91+15867i others(8): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406241 | ||||||
| chr11:1406243
|
G | C | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+15868G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406243 | ||||||
| chr11:1406244
|
C | A | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+15869C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406244 | ||||||
| chr11:1406300
|
A | G | 2 | a0001c0001t0003g0263a0001c0001t0011g0307 | 2 | NA18994.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.91+15925A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406300 | ||||||
| chr11:1406376
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+16001G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406376 | ||||||
| chr11:1406378
|
G | A | 23 | a0001c0001t0001g0113a0001c0001t0001g0154a0001c0001t0001g0189others(20): Show | 23 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.91+16003G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406378 | ||||||
| chr11:1406545
|
TG | T | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+16176delG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1406545 | |||||
| chr11:1406585
|
C | T | 5 | a0001c0001t0031g0012a0001c0001t0032g0195a0001c0001t0032g0209others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+16210C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406585 | ||||||
| chr11:1406700
|
G | A | 3 | a0002c0002t0019g0021a0002c0002t0019g0042a0002c0002t0019g0043 | 3 | HG02280.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.91+16325G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406700 | ||||||
| chr11:1406747
|
G | A | 22 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(19): Show | 22 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.91+16372G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406747 | ||||||
| chr11:1406846
|
G | A | 1 | a0002c0002t0007g0351 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.91+16471G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406846 | ||||||
| chr11:1406908
|
G | A | 23 | a0001c0001t0001g0113a0001c0001t0001g0154a0001c0001t0001g0189others(20): Show | 23 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.91+16533G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406908 | ||||||
| chr11:1406947
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+16572G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406947 | ||||||
| chr11:1406950
|
C | T | 1 | a0002c0002t0010g0004 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.91+16575C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406950 | ||||||
| chr11:1406965
|
G | C | 1 | a0001c0001t0062g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.91+16590G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1406965 | ||||||
| chr11:1407079
|
G | A | 19 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0134others(16): Show | 19 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.91+16704G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1407079 | ||||||
| chr11:1407134
|
C | T | 1 | a0001c0001t0004g0084 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.91+16759C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1407134 | ||||||
| chr11:1407146
|
C | T | 2 | a0001c0003t0001g0115a0001c0003t0001g0146 | 2 | HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.91+16771C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1407146 | ||||||
| chr11:1407358
|
C | A | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+16983C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1407358 | ||||||
| chr11:1407432
|
C | T | 1 | a0002c0002t0010g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.91+17057C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1407432 | ||||||
| chr11:1407550
|
A | G | 205 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.91+17175A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1407550 | ||||||
| chr11:1407626
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+17251C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1407626 | ||||||
| chr11:1407820
|
C | G | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 73 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.91+17445C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1407820 | ||||||
| chr11:1407932
|
G | A | 46 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(43): Show | 47 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.91+17557G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1407932 | ||||||
| chr11:1408163
|
G | A | 3 | a0002c0002t0007g0302a0002c0002t0007g0306a0002c0002t0017g0305 | 3 | NA18990.hp2 NA18993.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.91+17788G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408163 | ||||||
| chr11:1408386
|
G | A | 77 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 78 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.91+18011G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408386 | ||||||
| chr11:1408569
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+18194T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408569 | ||||||
| chr11:1408658
|
C | T | 51 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 52 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.91+18283C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408658 | ||||||
| chr11:1408764
|
G | GGT | 6 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(3): Show | 6 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+18402_91+18403d others(4): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1408764 | |||||
| chr11:1408776
|
TGTTTGG | T | 126 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.91+18402_91+18407d others(8): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408776 | ||||||
| chr11:1408779
|
TTGGC | T | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 73 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.91+18407_91+18410d others(6): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1408779 | |||||
| chr11:1408783
|
C | T | 126 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.91+18408C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408783 | ||||||
| chr11:1408811
|
TGG | T | 4 | a0001c0001t0003g0228a0001c0001t0013g0022a0001c0001t0013g0311others(1): Show | 4 | HG02145.hp2 HG02630.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+18437_91+18438d others(4): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408811 | ||||||
| chr11:1408812
|
G | GGT | 71 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0072others(68): Show | 73 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.91+18459_91+18460d others(4): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1408812 | |||||
| chr11:1408812
|
G | T | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(37): Show | 41 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.91+18437G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408812 | ||||||
| chr11:1408832
|
T | G | 1 | a0001c0001t0045g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.91+18457T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408832 | ||||||
| chr11:1408832
|
T | TGGG | 4 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(1): Show | 4 | HG01192.hp1 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+18458_91+18459i others(5): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1408832 | |||||
| chr11:1408834
|
T | G | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+18459T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408834 | ||||||
| chr11:1408860
|
T | G | 1 | a0001c0003t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.91+18485T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408860 | ||||||
| chr11:1408932
|
G | A | 3 | a0001c0001t0004g0314a0001c0001t0004g0316a0002c0002t0002g0318 | 3 | HG01943.hp1 HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.91+18557G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408932 | ||||||
| chr11:1408960
|
C | T | 25 | a0001c0001t0001g0046a0001c0001t0001g0113a0001c0001t0001g0154others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.91+18585C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408960 | ||||||
| chr11:1408969
|
T | G | 124 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(121): Show | 126 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.91+18594T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408969 | ||||||
| chr11:1408971
|
T | G | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+18596T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1408971 | ||||||
| chr11:1408984
|
GTGTA | G | 25 | a0001c0001t0001g0046a0001c0001t0001g0113a0001c0001t0001g0154others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.91+18613_91+18616d others(6): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1408984 | |||||
| chr11:1408986
|
GTA | G | 47 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(44): Show | 48 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.91+18613_91+18614d others(4): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1408986 | |||||
| chr11:1409056
|
A | G | 134 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0049others(131): Show | 135 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.91+18681A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409056 | ||||||
| chr11:1409056
|
A | T | 71 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(68): Show | 72 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.91+18681A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409056 | ||||||
| chr11:1409231
|
G | A | 23 | a0001c0001t0001g0113a0001c0001t0001g0154a0001c0001t0001g0189others(20): Show | 23 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.91+18856G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409231 | ||||||
| chr11:1409282
|
C | T | 1 | a0001c0001t0075g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+18907C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409282 | ||||||
| chr11:1409393
|
T | G | 1 | a0001c0001t0001g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.91+19018T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409393 | ||||||
| chr11:1409425
|
C | T | 26 | a0001c0001t0001g0046a0001c0001t0001g0113a0001c0001t0001g0154others(23): Show | 26 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.91+19050C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409425 | ||||||
| chr11:1409491
|
A | G | 52 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(49): Show | 53 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.91+19116A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409491 | ||||||
| chr11:1409539
|
T | C | 77 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 78 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.91+19164T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409539 | ||||||
| chr11:1409550
|
C | T | 129 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 130 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.91+19175C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409550 | ||||||
| chr11:1409552
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.91+19177G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409552 | ||||||
| chr11:1409560
|
T | C | 127 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(124): Show | 128 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.91+19185T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409560 | ||||||
| chr11:1409569
|
G | C | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 79 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.91+19194G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409569 | ||||||
| chr11:1409603
|
C | T | 1 | a0005c0010t0002g0085 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.91+19228C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409603 | ||||||
| chr11:1409626
|
G | A | 1 | a0001c0001t0003g0241 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.91+19251G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409626 | ||||||
| chr11:1409673
|
G | T | 31 | a0001c0001t0001g0127a0001c0001t0001g0141a0001c0001t0004g0136others(28): Show | 31 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.91+19298G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409673 | ||||||
| chr11:1409686
|
T | C | 259 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(256): Show | 262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.91+19311T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409686 | ||||||
| chr11:1409853
|
C | T | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 73 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.91+19478C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409853 | ||||||
| chr11:1409867
|
G | A | 1 | a0001c0001t0078g0205 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.91+19492G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409867 | ||||||
| chr11:1409904
|
A | AGAGTCCG others(76): Show |
7 | a0002c0002t0005g0211a0002c0002t0005g0260a0002c0002t0005g0281others(4): Show | 7 | HG01346.hp1 HG01934.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+19553_91+19635d others(85): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1409904 | |||||
| chr11:1409923
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.91+19548G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409923 | ||||||
| chr11:1409957
|
C | A | 1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.91+19582C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409957 | ||||||
| chr11:1409991
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.91+19616T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1409991 | ||||||
| chr11:1409993
|
CGTGTTTG others(76): Show |
C | 25 | a0001c0001t0001g0046a0001c0001t0001g0113a0001c0001t0001g0154others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.91+19700_91+19782d others(85): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1409993 | |||||
| chr11:1410037
|
G | A | 3 | a0002c0002t0038g0297a0002c0002t0040g0298a0002c0002t0071g0249 | 3 | HG01255.hp1 HG02602.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.91+19662G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410037 | ||||||
| chr11:1410076
|
T | C | 5 | a0001c0003t0014g0036a0001c0003t0014g0037a0001c0003t0014g0038others(2): Show | 5 | HG00642.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+19701T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410076 | ||||||
| chr11:1410207
|
A | ACAGAGTC others(161): Show |
1 | a0002c0002t0051g0077 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.91+19908_91+20075d others(170): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1410207 | |||||
| chr11:1410207
|
ACAGAGTC others(49): Show |
A | 23 | a0001c0001t0001g0058a0001c0003t0001g0070a0001c0003t0001g0114others(20): Show | 23 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.91+19940_91+19995d others(58): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1410207 | |||||
| chr11:1410207
|
ACAGAGTC others(105): Show |
A | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91+19884_91+19995d others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1410207 | |||||
| chr11:1410207
|
ACAGAGTC others(161): Show |
A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+19908_91+20075d others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1410207 | |||||
| chr11:1410215
|
C | T | 1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.91+19840C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410215 | ||||||
| chr11:1410262
|
TGCAGAGT others(105): Show |
T | 2 | a0001c0001t0032g0209a0001c0001t0070g0210 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.91+19964_91+20075d others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1410262 | |||||
| chr11:1410296
|
G | A | 45 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 46 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.91+19921G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410296 | ||||||
| chr11:1410308
|
C | T | 1 | a0001c0001t0046g0083 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.91+19933C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410308 | ||||||
| chr11:1410318
|
T | GGCAGAGT others(49): Show |
1 | a0002c0002t0002g0126 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.91+19943delTinsGGC others(54): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410318 | ||||||
| chr11:1410348
|
C | T | 1 | a0002c0002t0020g0125 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.91+19973C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410348 | ||||||
| chr11:1410407
|
C | T | 2 | a0001c0001t0003g0222a0001c0001t0065g0256 | 2 | NA18963.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.91+20032C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410407 | ||||||
| chr11:1410408
|
G | A | 1 | a0002c0002t0002g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.91+20033G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410408 | ||||||
| chr11:1410421
|
G | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(67): Show | 71 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.91+20046G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410421 | ||||||
| chr11:1410431
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0059g0041 | 3 | HG02055.hp2 HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.91+20056G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410431 | ||||||
| chr11:1410449
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+20074G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410449 | ||||||
| chr11:1410450
|
G | T | 2 | a0002c0005t0034g0055a0002c0005t0034g0056 | 2 | HG01346.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.91+20075G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410450 | ||||||
| chr11:1410455
|
G | A | 1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.91+20080G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410455 | ||||||
| chr11:1410506
|
G | A | 1 | a0002c0002t0020g0148 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.91+20131G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410506 | ||||||
| chr11:1410548
|
C | T | 1 | a0002c0002t0002g0088 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.91+20173C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410548 | ||||||
| chr11:1410594
|
C | T | 2 | a0001c0001t0014g0039a0001c0001t0045g0040 | 2 | HG01192.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.91+20219C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410594 | ||||||
| chr11:1410700
|
C | A | 23 | a0001c0001t0001g0113a0001c0001t0001g0154a0001c0001t0001g0189others(20): Show | 23 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.91+20325C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410700 | ||||||
| chr11:1410807
|
C | T | 23 | a0001c0001t0001g0192a0001c0003t0001g0070a0001c0003t0001g0114others(20): Show | 23 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.91+20432C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410807 | ||||||
| chr11:1410849
|
G | A | 1 | a0001c0001t0075g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+20474G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410849 | ||||||
| chr11:1410888
|
C | T | 2 | a0002c0005t0034g0055a0002c0005t0034g0056 | 2 | HG01346.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.91+20513C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1410888 | ||||||
| chr11:1411016
|
C | G | 1 | a0001c0003t0001g0338 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.91+20641C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411016 | ||||||
| chr11:1411016
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.91+20641C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411016 | ||||||
| chr11:1411058
|
A | C | 1 | a0002c0002t0010g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.91+20683A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411058 | ||||||
| chr11:1411151
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+20776C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411151 | ||||||
| chr11:1411191
|
C | G | 23 | a0001c0001t0001g0113a0001c0001t0001g0154a0001c0001t0001g0189others(20): Show | 23 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.91+20816C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411191 | ||||||
| chr11:1411305
|
C | T | 1 | a0002c0002t0017g0301 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.91+20930C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411305 | ||||||
| chr11:1411447
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+21072C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411447 | ||||||
| chr11:1411461
|
T | C | 73 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 74 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.91+21086T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411461 | ||||||
| chr11:1411669
|
C | T | 1 | a0002c0002t0023g0223 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.91+21294C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411669 | ||||||
| chr11:1411719
|
C | T | 23 | a0001c0001t0001g0168a0001c0001t0001g0186a0001c0001t0001g0317others(20): Show | 23 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.91+21344C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411719 | ||||||
| chr11:1411852
|
G | A | 3 | a0001c0001t0003g0265a0001c0001t0003g0271a0001c0001t0061g0266 | 3 | NA18969.hp1 NA19079.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.91+21477G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411852 | ||||||
| chr11:1411863
|
C | A | 2 | a0001c0001t0006g0229a0001c0001t0006g0248 | 2 | HG02683.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.91+21488C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411863 | ||||||
| chr11:1411955
|
A | AGTCCTGC others(29): Show |
2 | a0001c0001t0028g0332a0001c0001t0028g0333 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.91+21611_91+21612i others(38): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1411955 | |||||
| chr11:1411955
|
A | AGTCCTGC others(29): Show |
37 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(34): Show | 38 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.91+21782_91+21817d others(38): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1411955 | |||||
| chr11:1411955
|
A | AGTCCTGC others(65): Show |
1 | a0001c0001t0003g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+21746_91+21817d others(74): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1411955 | |||||
| chr11:1411955
|
AGTCCTGC others(29): Show |
A | 5 | a0001c0003t0014g0036a0001c0003t0014g0037a0001c0003t0014g0038others(2): Show | 5 | HG00642.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+21782_91+21817d others(38): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1411955 | |||||
| chr11:1411963
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.91+21588G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411963 | ||||||
| chr11:1411965
|
T | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG01943.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.91+21590T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411965 | ||||||
| chr11:1411991
|
C | T | 23 | a0001c0001t0001g0113a0001c0001t0001g0154a0001c0001t0001g0189others(20): Show | 23 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.91+21616C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1411991 | ||||||
| chr11:1412023
|
G | A | 2 | a0001c0001t0001g0127a0002c0002t0023g0254 | 2 | HG03239.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.91+21648G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412023 | ||||||
| chr11:1412056
|
G | A | 53 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(50): Show | 53 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.91+21681G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412056 | ||||||
| chr11:1412064
|
G | A | 1 | a0002c0002t0040g0298 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.91+21689G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412064 | ||||||
| chr11:1412070
|
CGGTGGGT others(389): Show |
C | 1 | a0002c0002t0049g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.91+21716_91+22111d others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1412070 | |||||
| chr11:1412084
|
T | C | 1 | a0002c0002t0010g0233 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.91+21709T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412084 | ||||||
| chr11:1412120
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.91+21745T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412120 | ||||||
| chr11:1412121
|
CAGCTGCG others(389): Show |
C | 2 | a0001c0001t0003g0228a0001c0001t0004g0121 | 2 | HG02129.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.91+21752_91+22147d others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1412121 | |||||
| chr11:1412122
|
A | G | 1 | a0002c0002t0008g0181 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.91+21747A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412122 | ||||||
| chr11:1412135
|
C | T | 2 | a0002c0002t0005g0259a0002c0002t0010g0246 | 2 | HG02132.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.91+21760C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412135 | ||||||
| chr11:1412156
|
T | C | 94 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(91): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.91+21781T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412156 | ||||||
| chr11:1412157
|
CAGCTGCG others(29): Show |
C | 1 | a0001c0001t0003g0235 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.91+21818_91+21853d others(38): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1412157 | |||||
| chr11:1412157
|
CAGCTGCG others(353): Show |
C | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(67): Show | 71 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.91+21788_91+22147d others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1412157 | |||||
| chr11:1412166
|
C | T | 1 | a0002c0002t0008g0151 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.91+21791C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412166 | ||||||
| chr11:1412166
|
CGCCCCGT others(245): Show |
C | 94 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(91): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.91+21818_91+22069d others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1412166 | |||||
| chr11:1412178
|
CGGTGGGT others(281): Show |
C | 1 | a0001c0001t0001g0102 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.91+21818_91+22105d others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1412178 | |||||
| chr11:1412192
|
T | C | 1 | a0002c0002t0015g0027 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.91+21817T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412192 | ||||||
| chr11:1412193
|
G | C | 61 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(58): Show | 62 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.91+21818G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412193 | ||||||
| chr11:1412193
|
G | GAGCTGCG others(29): Show |
1 | a0002c0002t0002g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.91+21998_91+22033d others(38): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1412193 | |||||
| chr11:1412229
|
C | CAGCTGCG others(101): Show |
1 | a0002c0002t0002g0132 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.91+21961_91+21962i others(110): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1412229 | |||||
| chr11:1412229
|
C | G | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+21854C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412229 | ||||||
| chr11:1412250
|
CGGTGGGT others(209): Show |
C | 1 | a0002c0002t0015g0027 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.91+21896_91+22111d others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1412250 | |||||
| chr11:1412265
|
C | G | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+21890C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412265 | ||||||
| chr11:1412300
|
T | C | 1 | a0001c0003t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.91+21925T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412300 | ||||||
| chr11:1412336
|
T | C | 17 | a0001c0001t0001g0127a0001c0001t0001g0141a0001c0001t0004g0136others(14): Show | 17 | HG00140.hp2 HG01099.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.91+21961T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412336 | ||||||
| chr11:1412346
|
CGCCCCGT others(65): Show |
C | 2 | a0002c0002t0007g0351a0002c0002t0017g0353 | 2 | NA18975.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.91+22019_91+22090d others(74): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1412346 | |||||
| chr11:1412372
|
T | C | 22 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(19): Show | 22 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.91+21997T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412372 | ||||||
| chr11:1412373
|
C | G | 1 | a0002c0002t0007g0304 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.91+21998C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412373 | ||||||
| chr11:1412382
|
CGCCCCGT others(29): Show |
C | 22 | a0001c0001t0001g0048a0001c0001t0001g0313a0001c0001t0003g0232others(19): Show | 23 | HG01192.hp1 HG01952.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.91+22034_91+22069d others(38): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1412382 | |||||
| chr11:1412394
|
CGGTGGGT others(65): Show |
C | 8 | a0001c0001t0001g0127a0001c0001t0001g0141a0001c0001t0004g0136others(5): Show | 8 | HG00140.hp2 HG01099.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+22034_91+22105d others(74): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1412394 | |||||
| chr11:1412408
|
T | C | 22 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(19): Show | 22 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.91+22033T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412408 | ||||||
| chr11:1412409
|
G | C | 26 | a0001c0001t0001g0192a0001c0001t0003g0235a0001c0003t0001g0070others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.91+22034G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412409 | ||||||
| chr11:1412418
|
T | C | 34 | a0001c0001t0001g0192a0001c0001t0003g0194a0001c0001t0003g0196others(31): Show | 34 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.91+22043T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412418 | ||||||
| chr11:1412444
|
T | C | 22 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(19): Show | 22 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.91+22069T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412444 | ||||||
| chr11:1412460
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG00408.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.91+22085G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412460 | ||||||
| chr11:1412466
|
T | C | 126 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0057others(123): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.91+22091T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412466 | ||||||
| chr11:1412576
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+22201C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412576 | ||||||
| chr11:1412621
|
C | T | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 79 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.91+22246C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412621 | ||||||
| chr11:1412625
|
G | A | 1 | a0002c0002t0002g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.91+22250G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412625 | ||||||
| chr11:1412666
|
G | T | 205 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.91+22291G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412666 | ||||||
| chr11:1412702
|
G | A | 3 | a0001c0001t0003g0193a0001c0001t0028g0332a0001c0001t0028g0333 | 3 | HG00280.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.91+22327G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412702 | ||||||
| chr11:1412811
|
A | AGCCCTGG others(41): Show |
5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+22461_91+22462i others(50): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1412811 | |||||
| chr11:1412906
|
G | A | 127 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(124): Show | 128 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.91+22531G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412906 | ||||||
| chr11:1412917
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.91+22542G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412917 | ||||||
| chr11:1412942
|
A | G | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+22567A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412942 | ||||||
| chr11:1412982
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+22607C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1412982 | ||||||
| chr11:1413122
|
G | A | 2 | a0001c0001t0004g0173a0001c0001t0004g0188 | 2 | HG03239.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.91+22747G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413122 | ||||||
| chr11:1413214
|
C | T | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 73 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.92-22826C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413214 | ||||||
| chr11:1413221
|
T | G | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-22819T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413221 | ||||||
| chr11:1413238
|
G | A | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.92-22802G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413238 | ||||||
| chr11:1413265
|
G | T | 1 | a0001c0001t0001g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.92-22775G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413265 | ||||||
| chr11:1413324
|
C | G | 1 | a0001c0003t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.92-22716C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413324 | ||||||
| chr11:1413324
|
C | T | 1 | a0001c0001t0003g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-22716C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413324 | ||||||
| chr11:1413349
|
G | A | 2 | a0001c0001t0001g0046a0001c0003t0003g0291 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.92-22691G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413349 | ||||||
| chr11:1413354
|
G | C | 1 | a0001c0001t0001g0089 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.92-22686G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413354 | ||||||
| chr11:1413450
|
T | C | 206 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(203): Show | 208 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.92-22590T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413450 | ||||||
| chr11:1413454
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-22586G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413454 | ||||||
| chr11:1413529
|
C | T | 25 | a0001c0001t0001g0046a0001c0001t0001g0113a0001c0001t0001g0154others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.92-22511C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413529 | ||||||
| chr11:1413536
|
C | T | 4 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0099others(1): Show | 4 | NA18939.hp2 NA18940.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-22504C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413536 | ||||||
| chr11:1413718
|
A | G | 1 | a0002c0002t0007g0346 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.92-22322A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413718 | ||||||
| chr11:1413871
|
G | A | 1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.92-22169G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413871 | ||||||
| chr11:1413913
|
T | C | 204 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(201): Show | 206 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.92-22127T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413913 | ||||||
| chr11:1413920
|
T | C | 258 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(255): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.92-22120T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1413920 | ||||||
| chr11:1414099
|
G | A | 204 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(201): Show | 206 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.92-21941G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414099 | ||||||
| chr11:1414149
|
C | T | 204 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(201): Show | 206 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.92-21891C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414149 | ||||||
| chr11:1414167
|
G | A | 2 | a0001c0003t0001g0114a0001c0003t0001g0134 | 2 | NA18970.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.92-21873G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414167 | ||||||
| chr11:1414296
|
A | T | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92-21744A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414296 | ||||||
| chr11:1414298
|
G | C | 127 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(124): Show | 128 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.92-21742G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414298 | ||||||
| chr11:1414347
|
A | G | 2 | a0001c0003t0001g0115a0001c0003t0001g0146 | 2 | HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.92-21693A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414347 | ||||||
| chr11:1414359
|
G | A | 1 | a0002c0002t0005g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.92-21681G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414359 | ||||||
| chr11:1414465
|
C | T | 1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.92-21575C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414465 | ||||||
| chr11:1414499
|
C | A | 13 | a0001c0001t0001g0044a0001c0001t0001g0312a0001c0001t0003g0199others(10): Show | 13 | HG00642.hp1 HG01070.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.92-21541C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414499 | ||||||
| chr11:1414568
|
G | T | 1 | a0001c0001t0003g0241 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.92-21472G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414568 | ||||||
| chr11:1414622
|
C | T | 6 | a0001c0001t0001g0066a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 6 | HG01123.hp1 HG01256.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-21418C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414622 | ||||||
| chr11:1414623
|
A | G | 204 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(201): Show | 206 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.92-21417A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414623 | ||||||
| chr11:1414645
|
C | T | 1 | a0001c0001t0006g0226 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.92-21395C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414645 | ||||||
| chr11:1414663
|
C | T | 2 | a0001c0001t0001g0046a0001c0003t0003g0291 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.92-21377C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414663 | ||||||
| chr11:1414664
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0003g0002others(2): Show | 6 | HG02572.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-21376G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414664 | ||||||
| chr11:1414735
|
C | T | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 73 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.92-21305C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414735 | ||||||
| chr11:1414756
|
T | C | 1 | a0002c0002t0016g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.92-21284T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414756 | ||||||
| chr11:1414824
|
G | C | 127 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(124): Show | 128 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.92-21216G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414824 | ||||||
| chr11:1414830
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92-21210G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414830 | ||||||
| chr11:1414916
|
G | A | 127 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(124): Show | 128 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.92-21124G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1414916 | ||||||
| chr11:1415094
|
C | CT | 25 | a0001c0001t0001g0011a0001c0001t0032g0209a0001c0003t0001g0070others(22): Show | 25 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.92-20928dupT | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1415094 | |||||
| chr11:1415094
|
C | CTT | 102 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(99): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.92-20929_92-20928d others(4): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1415094 | |||||
| chr11:1415094
|
CT | C | 28 | a0001c0001t0001g0046a0001c0001t0001g0113a0001c0001t0001g0123others(25): Show | 28 | HG00639.hp2 HG01069.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.92-20928delT | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1415094 | |||||
| chr11:1415156
|
G | A | 9 | a0001c0001t0001g0127a0001c0001t0001g0141a0001c0001t0004g0136others(6): Show | 9 | HG00140.hp2 HG01099.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-20884G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1415156 | ||||||
| chr11:1415193
|
G | C | 127 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(124): Show | 128 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.92-20847G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1415193 | ||||||
| chr11:1415341
|
G | A | 1 | a0002c0002t0007g0308 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.92-20699G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1415341 | ||||||
| chr11:1415484
|
G | C | 204 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(201): Show | 206 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.92-20556G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1415484 | ||||||
| chr11:1415538
|
C | G | 1 | a0001c0001t0075g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.92-20502C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1415538 | ||||||
| chr11:1415540
|
G | A | 1 | a0002c0002t0002g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.92-20500G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1415540 | ||||||
| chr11:1415771
|
GTGGTCCC others(11): Show |
G | 128 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(125): Show | 129 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.92-20247_92-20230d others(20): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1415771 | |||||
| chr11:1415799
|
C | A | 1 | a0001c0001t0004g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.92-20241C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1415799 | ||||||
| chr11:1415980
|
A | G | 1 | a0002c0002t0007g0346 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.92-20060A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1415980 | ||||||
| chr11:1416009
|
A | G | 26 | a0001c0001t0001g0113a0001c0001t0001g0154a0001c0001t0001g0189others(23): Show | 27 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.92-20031A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416009 | ||||||
| chr11:1416067
|
C | T | 127 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(124): Show | 128 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.92-19973C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416067 | ||||||
| chr11:1416259
|
C | T | 1 | a0002c0002t0007g0309 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.92-19781C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416259 | ||||||
| chr11:1416280
|
C | T | 1 | a0002c0002t0058g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-19760C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416280 | ||||||
| chr11:1416290
|
G | A | 1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.92-19750G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416290 | ||||||
| chr11:1416364
|
G | A | 2 | a0001c0003t0001g0115a0001c0003t0001g0146 | 2 | HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.92-19676G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416364 | ||||||
| chr11:1416489
|
C | T | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-19551C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416489 | ||||||
| chr11:1416528
|
C | G | 46 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(43): Show | 47 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.92-19512C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416528 | ||||||
| chr11:1416549
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.92-19491C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416549 | ||||||
| chr11:1416552
|
T | C | 204 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(201): Show | 206 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.92-19488T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416552 | ||||||
| chr11:1416728
|
G | A | 1 | a0002c0002t0002g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92-19312G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416728 | ||||||
| chr11:1416742
|
G | A | 1 | a0001c0001t0059g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-19298G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416742 | ||||||
| chr11:1416856
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-19184C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416856 | ||||||
| chr11:1416873
|
T | C | 204 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(201): Show | 206 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.92-19167T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416873 | ||||||
| chr11:1416887
|
G | A | 2 | a0001c0001t0064g0261a0004c0009t0008g0178 | 2 | HG02055.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.92-19153G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416887 | ||||||
| chr11:1416935
|
C | T | 3 | a0001c0001t0003g0194a0001c0001t0003g0196a0001c0001t0003g0237 | 3 | HG02559.hp1 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.92-19105C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416935 | ||||||
| chr11:1416943
|
G | A | 3 | a0001c0001t0009g0153a0002c0002t0008g0151a0005c0010t0002g0085 | 3 | HG00408.hp2 NA18612.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.92-19097G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416943 | ||||||
| chr11:1416953
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.92-19087G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1416953 | ||||||
| chr11:1417145
|
C | T | 2 | a0001c0001t0003g0228a0002c0002t0005g0281 | 2 | HG01993.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.92-18895C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1417145 | ||||||
| chr11:1417296
|
T | A | 13 | a0002c0002t0002g0013a0002c0002t0002g0014a0002c0002t0002g0018others(10): Show | 13 | HG01109.hp2 HG01433.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.92-18744T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1417296 | ||||||
| chr11:1417449
|
C | G | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-18591C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1417449 | ||||||
| chr11:1417478
|
ACCTGTGT others(563): Show |
A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-18505_92-17936d others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1417478 | |||||
| chr11:1417535
|
A | C | 125 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.92-18505A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1417535 | ||||||
| chr11:1417535
|
A | T | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 79 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.92-18505A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1417535 | ||||||
| chr11:1417622
|
C | CCTGTGTC others(41): Show |
168 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(165): Show | 170 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.92-18274_92-18227d others(50): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1417622 | |||||
| chr11:1417732
|
C | CTGTTGGC others(41): Show |
5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-18261_92-18260i others(50): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1417732 | |||||
| chr11:1417784
|
T | TGGCTGTT others(41): Show |
25 | a0001c0001t0001g0046a0001c0001t0001g0154a0001c0001t0001g0189others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.92-18227_92-18226i others(50): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1417784 | |||||
| chr11:1417784
|
TGGCTGTT others(40): Show |
T | 1 | a0002c0002t0007g0304 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.92-18179_92-18133d others(49): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1417784 | |||||
| chr11:1417813
|
C | CACTGTGT others(421): Show |
1 | a0001c0016t0018g0183 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.92-18227_92-18226i others(430): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1417813 | ||||||
| chr11:1417813
|
C | CCTGTGTC others(420): Show |
24 | a0001c0001t0001g0046a0001c0001t0001g0189a0001c0001t0001g0191others(21): Show | 24 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.92-18164_92-17738d others(429): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1417813 | |||||
| chr11:1417831
|
G | T | 2 | a0001c0001t0006g0247a0002c0002t0015g0330 | 2 | HG01175.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.92-18209G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1417831 | ||||||
| chr11:1417878
|
G | T | 2 | a0001c0001t0001g0058a0002c0005t0005g0289 | 2 | HG03579.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.92-18162G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1417878 | ||||||
| chr11:1417906
|
ACACTGTG others(41): Show |
A | 2 | a0001c0001t0006g0247a0002c0002t0015g0330 | 2 | HG01175.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.92-18132_92-18085d others(50): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1417906 | |||||
| chr11:1417973
|
T | G | 2 | a0001c0001t0006g0247a0002c0002t0015g0330 | 2 | HG01175.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.92-18067T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1417973 | ||||||
| chr11:1418069
|
G | T | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-17971G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418069 | ||||||
| chr11:1418096
|
CACTGTGT others(42): Show |
C | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-17943_92-17895d others(51): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418096 | ||||||
| chr11:1418163
|
T | G | 1 | a0002c0002t0056g0337 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.92-17877T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418163 | ||||||
| chr11:1418167
|
T | A | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-17873T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418167 | ||||||
| chr11:1418174
|
T | C | 1 | a0002c0002t0002g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.92-17866T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418174 | ||||||
| chr11:1418181
|
T | A | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-17859T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418181 | ||||||
| chr11:1418188
|
G | T | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-17852G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418188 | ||||||
| chr11:1418191
|
A | T | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-17849A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418191 | ||||||
| chr11:1418210
|
G | T | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-17830G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418210 | ||||||
| chr11:1418210
|
GGGCTGTT others(90): Show |
G | 1 | a0001c0001t0025g0147 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.92-17800_92-17704d others(99): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1418210 | |||||
| chr11:1418235
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-17805G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418235 | ||||||
| chr11:1418258
|
G | T | 2 | a0002c0002t0005g0250a0002c0002t0015g0330 | 2 | HG02258.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.92-17782G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418258 | ||||||
| chr11:1418301
|
C | CTGTGGGC others(133): Show |
1 | a0001c0001t0001g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.92-17738_92-17737i others(142): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1418301 | |||||
| chr11:1418311
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.92-17729T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418311 | ||||||
| chr11:1418325
|
A | T | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-17715A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418325 | ||||||
| chr11:1418332
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.92-17708G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418332 | ||||||
| chr11:1418335
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.92-17705A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418335 | ||||||
| chr11:1418354
|
T | G | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-17686T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418354 | ||||||
| chr11:1418356
|
T | G | 2 | a0001c0001t0001g0154a0002c0002t0015g0330 | 2 | HG02258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.92-17684T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418356 | ||||||
| chr11:1418388
|
A | G | 2 | a0001c0001t0001g0154a0002c0002t0015g0330 | 2 | HG02258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.92-17652A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418388 | ||||||
| chr11:1418401
|
T | G | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-17639T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418401 | ||||||
| chr11:1418436
|
G | GTCCTGCT others(231): Show |
1 | a0001c0001t0001g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.92-17574_92-17573i others(240): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1418436 | |||||
| chr11:1418497
|
G | T | 104 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(101): Show | 105 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.92-17543G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418497 | ||||||
| chr11:1418514
|
G | C | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-17526G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418514 | ||||||
| chr11:1418544
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.92-17496T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418544 | ||||||
| chr11:1418661
|
G | A | 24 | a0001c0001t0001g0154a0001c0001t0001g0189a0001c0001t0001g0191others(21): Show | 24 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.92-17379G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418661 | ||||||
| chr11:1418664
|
G | T | 94 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(91): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.92-17376G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418664 | ||||||
| chr11:1418691
|
G | A | 4 | a0001c0001t0032g0195a0001c0001t0032g0209a0001c0001t0070g0210others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-17349G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418691 | ||||||
| chr11:1418833
|
C | T | 1 | a0001c0001t0065g0256 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.92-17207C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1418833 | ||||||
| chr11:1419145
|
T | C | 204 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(201): Show | 206 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.92-16895T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1419145 | ||||||
| chr11:1419148
|
C | CG | 51 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(48): Show | 52 | HG00323.hp2 HG00741.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.92-16884dupG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1419148 | |||||
| chr11:1419155
|
G | A | 125 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.92-16885G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1419155 | ||||||
| chr11:1419249
|
T | C | 53 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(50): Show | 54 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.92-16791T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1419249 | ||||||
| chr11:1419291
|
G | A | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.92-16749G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1419291 | ||||||
| chr11:1419318
|
G | A | 46 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(43): Show | 47 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.92-16722G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1419318 | ||||||
| chr11:1419528
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-16512T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1419528 | ||||||
| chr11:1419546
|
G | T | 126 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.92-16494G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1419546 | ||||||
| chr11:1419891
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.92-16149C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1419891 | ||||||
| chr11:1419949
|
T | C | 1 | a0001c0001t0009g0122 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.92-16091T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1419949 | ||||||
| chr11:1419949
|
TTCCTGAG others(9): Show |
T | 9 | a0001c0001t0001g0127a0001c0001t0001g0141a0001c0001t0004g0136others(6): Show | 9 | HG00140.hp2 HG01099.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-16087_92-16072d others(18): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1419949 | |||||
| chr11:1419973
|
T | G | 22 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(19): Show | 22 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.92-16067T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1419973 | ||||||
| chr11:1419987
|
C | G | 1 | a0002c0002t0008g0078 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.92-16053C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1419987 | ||||||
| chr11:1420022
|
G | A | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.92-16018G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420022 | ||||||
| chr11:1420056
|
C | G | 4 | a0001c0001t0001g0087a0001c0001t0001g0107a0002c0002t0008g0157others(1): Show | 4 | HG00280.hp1 HG00609.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-15984C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420056 | ||||||
| chr11:1420153
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-15887C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420153 | ||||||
| chr11:1420170
|
G | A | 24 | a0001c0001t0001g0154a0001c0001t0001g0189a0001c0001t0001g0191others(21): Show | 24 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.92-15870G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420170 | ||||||
| chr11:1420213
|
C | G | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 79 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.92-15827C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420213 | ||||||
| chr11:1420244
|
G | A | 3 | a0001c0001t0004g0314a0001c0001t0004g0316a0002c0002t0002g0318 | 3 | HG01943.hp1 HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.92-15796G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420244 | ||||||
| chr11:1420254
|
T | C | 126 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.92-15786T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420254 | ||||||
| chr11:1420274
|
C | T | 1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.92-15766C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420274 | ||||||
| chr11:1420321
|
T | C | 1 | a0002c0002t0002g0133 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.92-15719T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420321 | ||||||
| chr11:1420323
|
T | C | 126 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.92-15717T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420323 | ||||||
| chr11:1420380
|
G | A | 1 | a0002c0002t0005g0262 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.92-15660G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420380 | ||||||
| chr11:1420482
|
A | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0003g0002others(2): Show | 6 | HG02572.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-15558A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420482 | ||||||
| chr11:1420513
|
G | A | 2 | a0001c0001t0003g0227a0001c0001t0003g0241 | 2 | HG01257.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.92-15527G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420513 | ||||||
| chr11:1420518
|
G | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 79 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.92-15522G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420518 | ||||||
| chr11:1420766
|
C | T | 126 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.92-15274C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420766 | ||||||
| chr11:1420929
|
C | T | 73 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 74 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.92-15111C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420929 | ||||||
| chr11:1420996
|
C | T | 125 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.92-15044C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1420996 | ||||||
| chr11:1421049
|
G | A | 1 | a0001c0001t0001g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.92-14991G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421049 | ||||||
| chr11:1421057
|
C | G | 2 | a0002c0002t0002g0169a0002c0002t0002g0170 | 2 | HG01099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.92-14983C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421057 | ||||||
| chr11:1421111
|
C | T | 1 | a0001c0001t0003g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.92-14929C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421111 | ||||||
| chr11:1421267
|
A | G | 1 | a0001c0001t0075g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.92-14773A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421267 | ||||||
| chr11:1421325
|
T | C | 206 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(203): Show | 208 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.92-14715T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421325 | ||||||
| chr11:1421432
|
A | G | 2 | a0002c0002t0002g0159a0002c0002t0020g0125 | 2 | HG02074.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.92-14608A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421432 | ||||||
| chr11:1421439
|
CTTTG | C | 7 | a0001c0001t0001g0073a0001c0001t0004g0080a0001c0001t0004g0081others(4): Show | 7 | HG00438.hp2 NA18939.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-14596_92-14593d others(6): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1421439 | |||||
| chr11:1421465
|
C | T | 1 | a0001c0001t0003g0002 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.92-14575C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421465 | ||||||
| chr11:1421526
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.92-14514G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421526 | ||||||
| chr11:1421538
|
A | G | 6 | a0001c0001t0001g0066a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 6 | HG01123.hp1 HG01256.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-14502A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421538 | ||||||
| chr11:1421554
|
C | T | 9 | a0001c0001t0001g0127a0001c0001t0001g0141a0001c0001t0004g0136others(6): Show | 9 | HG00140.hp2 HG01099.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-14486C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421554 | ||||||
| chr11:1421567
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-14473C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421567 | ||||||
| chr11:1421699
|
C | T | 3 | a0002c0002t0005g0264a0002c0002t0005g0276a0002c0002t0010g0275 | 3 | HG01175.hp2 NA18944.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.92-14341C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421699 | ||||||
| chr11:1421778
|
G | C | 3 | a0001c0001t0004g0314a0001c0001t0004g0316a0002c0002t0002g0318 | 3 | HG01943.hp1 HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.92-14262G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421778 | ||||||
| chr11:1421954
|
G | A | 26 | a0001c0001t0001g0046a0001c0001t0001g0154a0001c0001t0001g0189others(23): Show | 26 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.92-14086G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1421954 | ||||||
| chr11:1422032
|
C | T | 1 | a0002c0002t0058g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-14008C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422032 | ||||||
| chr11:1422052
|
G | A | 125 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(122): Show | 126 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.92-13988G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422052 | ||||||
| chr11:1422055
|
C | T | 333 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(330): Show | 338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.92-13985C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422055 | ||||||
| chr11:1422066
|
T | C | 256 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(253): Show | 259 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.92-13974T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422066 | ||||||
| chr11:1422067
|
G | A | 46 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(43): Show | 47 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.92-13973G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422067 | ||||||
| chr11:1422084
|
C | T | 126 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.92-13956C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422084 | ||||||
| chr11:1422168
|
C | T | 34 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0168others(31): Show | 35 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.92-13872C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422168 | ||||||
| chr11:1422216
|
C | G | 1 | a0001c0003t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.92-13824C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422216 | ||||||
| chr11:1422245
|
A | G | 2 | a0001c0001t0063g0253a0002c0002t0005g0198 | 2 | HG00639.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.92-13795A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422245 | ||||||
| chr11:1422323
|
G | T | 3 | a0001c0001t0001g0048a0001c0001t0043g0050a0002c0002t0002g0015 | 3 | HG02647.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.92-13717G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422323 | ||||||
| chr11:1422332
|
C | T | 94 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(91): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.92-13708C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422332 | ||||||
| chr11:1422454
|
C | T | 46 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(43): Show | 47 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.92-13586C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422454 | ||||||
| chr11:1422466
|
G | A | 42 | a0001c0001t0001g0044a0001c0001t0001g0312a0001c0001t0001g0339others(39): Show | 42 | HG00280.hp2 HG00642.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.92-13574G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422466 | ||||||
| chr11:1422518
|
A | G | 204 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(201): Show | 206 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.92-13522A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422518 | ||||||
| chr11:1422549
|
C | A | 182 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 184 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.92-13491C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422549 | ||||||
| chr11:1422612
|
C | T | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 73 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.92-13428C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422612 | ||||||
| chr11:1422654
|
C | G | 2 | a0001c0001t0001g0317a0001c0001t0011g0303 | 2 | NA18980.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.92-13386C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422654 | ||||||
| chr11:1422696
|
A | T | 1 | a0001c0001t0001g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.92-13344A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422696 | ||||||
| chr11:1422825
|
A | AG | 6 | a0001c0001t0001g0069a0001c0001t0003g0263a0001c0001t0018g0137others(3): Show | 6 | HG00408.hp2 HG01261.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-13210dupG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1422825 | |||||
| chr11:1422869
|
C | T | 1 | a0001c0003t0014g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.92-13171C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422869 | ||||||
| chr11:1422939
|
G | A | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(246): Show | 252 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.92-13101G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1422939 | ||||||
| chr11:1423011
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92-13029C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423011 | ||||||
| chr11:1423058
|
A | G | 2 | a0001c0003t0001g0115a0001c0003t0001g0146 | 2 | HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.92-12982A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423058 | ||||||
| chr11:1423069
|
C | G | 1 | a0001c0001t0003g0280 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.92-12971C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423069 | ||||||
| chr11:1423098
|
C | G | 108 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0057others(105): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.92-12942C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423098 | ||||||
| chr11:1423171
|
T | G | 1 | a0001c0001t0006g0218 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.92-12869T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423171 | ||||||
| chr11:1423180
|
C | T | 1 | a0002c0002t0005g0274 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.92-12860C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423180 | ||||||
| chr11:1423190
|
T | C | 2 | a0001c0001t0003g0228a0002c0005t0005g0289 | 2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.92-12850T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423190 | ||||||
| chr11:1423237
|
G | A | 1 | a0001c0001t0013g0311 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.92-12803G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423237 | ||||||
| chr11:1423243
|
G | A | 2 | a0001c0001t0001g0046a0001c0003t0003g0291 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.92-12797G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423243 | ||||||
| chr11:1423259
|
C | T | 1 | a0001c0006t0001g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.92-12781C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423259 | ||||||
| chr11:1423298
|
C | T | 22 | a0001c0001t0001g0154a0001c0001t0001g0189a0001c0001t0001g0191others(19): Show | 22 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.92-12742C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423298 | ||||||
| chr11:1423325
|
A | G | 2 | a0001c0001t0001g0046a0001c0003t0003g0291 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.92-12715A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423325 | ||||||
| chr11:1423338
|
T | C | 2 | a0002c0008t0002g0326a0002c0008t0005g0278 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.92-12702T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423338 | ||||||
| chr11:1423361
|
G | A | 2 | a0001c0001t0001g0072a0002c0002t0008g0078 | 2 | HG01496.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.92-12679G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423361 | ||||||
| chr11:1423369
|
G | T | 2 | a0002c0002t0005g0269a0002c0002t0020g0125 | 2 | HG02132.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.92-12671G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423369 | ||||||
| chr11:1423486
|
G | T | 1 | a0001c0003t0001g0070 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.92-12554G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423486 | ||||||
| chr11:1423659
|
C | CTGCCCCA others(25): Show |
1 | a0001c0001t0001g0102 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.92-12374_92-12373i others(34): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(185): Show |
1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.92-12374_92-12373i others(194): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(217): Show |
2 | a0001c0003t0014g0036a0001c0003t0031g0007 | 2 | HG00642.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.92-12374_92-12373i others(226): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(281): Show |
4 | a0001c0003t0014g0037a0001c0003t0014g0038a0001c0004t0001g0091others(1): Show | 4 | HG01433.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-12374_92-12373i others(290): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(313): Show |
14 | a0001c0003t0001g0070a0001c0003t0001g0134a0001c0003t0001g0135others(11): Show | 14 | HG00423.hp1 HG00558.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.92-12374_92-12373i others(322): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(377): Show |
2 | a0001c0001t0001g0343a0001c0001t0047g0340 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.92-12374_92-12373i others(386): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(409): Show |
2 | a0001c0001t0003g0234a0002c0002t0002g0035 | 2 | HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.92-12374_92-12373i others(418): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(537): Show |
1 | a0002c0005t0034g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92-12374_92-12373i others(546): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(569): Show |
1 | a0002c0005t0034g0056 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.92-12374_92-12373i others(578): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(313): Show |
1 | a0001c0003t0001g0114 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.92-12374_92-12373i others(322): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(377): Show |
1 | a0002c0002t0002g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.92-12374_92-12373i others(386): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(409): Show |
1 | a0002c0011t0002g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.92-12374_92-12373i others(418): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(281): Show |
1 | a0001c0001t0003g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.92-12374_92-12373i others(290): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(345): Show |
1 | a0001c0003t0001g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.92-12374_92-12373i others(354): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(377): Show |
1 | a0002c0002t0002g0014 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92-12374_92-12373i others(386): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(409): Show |
20 | a0001c0001t0001g0044a0001c0001t0001g0312a0001c0001t0003g0199others(17): Show | 20 | HG00642.hp1 HG01070.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-12374_92-12373i others(418): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(441): Show |
4 | a0001c0001t0003g0237a0001c0001t0003g0287a0002c0002t0029g0025others(1): Show | 4 | HG02258.hp2 HG02572.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-12374_92-12373i others(450): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(473): Show |
2 | a0001c0001t0003g0194a0001c0001t0003g0196 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.92-12374_92-12373i others(482): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(345): Show |
3 | a0001c0001t0028g0332a0001c0001t0028g0333a0002c0002t0002g0169 | 3 | HG01257.hp1 HG01258.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.92-12374_92-12373i others(354): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423659
|
C | CTGCCCCA others(377): Show |
8 | a0001c0001t0001g0339a0001c0001t0003g0193a0001c0001t0004g0173others(5): Show | 8 | HG00280.hp2 HG01081.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-12374_92-12373i others(386): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423659 | |||||
| chr11:1423667
|
A | AGCCTCCC others(185): Show |
2 | a0001c0001t0001g0189a0001c0001t0001g0191 | 2 | HG01123.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.92-12357_92-12356i others(194): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(217): Show |
1 | a0001c0001t0004g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.92-12357_92-12356i others(226): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(569): Show |
3 | a0001c0001t0004g0314a0001c0001t0004g0316a0002c0002t0002g0318 | 3 | HG01943.hp1 HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.92-12357_92-12356i others(578): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(665): Show |
1 | a0001c0001t0057g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.92-12357_92-12356i others(674): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(633): Show |
3 | a0001c0001t0006g0229a0001c0001t0006g0251a0001c0003t0003g0291 | 3 | HG02735.hp1 HG02735.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.92-12357_92-12356i others(642): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(666): Show |
1 | a0001c0001t0068g0243 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.92-12357_92-12356i others(675): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(665): Show |
10 | a0001c0001t0001g0154a0001c0001t0004g0161a0001c0001t0004g0172others(7): Show | 10 | HG00639.hp2 HG01192.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-12357_92-12356i others(674): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(697): Show |
2 | a0001c0001t0004g0175a0001c0001t0004g0179 | 2 | HG01361.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.92-12357_92-12356i others(706): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(729): Show |
2 | a0001c0001t0004g0180a0001c0001t0004g0185 | 2 | HG01069.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.92-12357_92-12356i others(738): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(729): Show |
1 | a0001c0001t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.92-12357_92-12356i others(738): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(25): Show |
4 | a0001c0001t0001g0130a0001c0001t0004g0051a0002c0002t0005g0276others(1): Show | 4 | HG01175.hp2 HG01243.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-12231_92-12200d others(34): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(89): Show |
1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92-12295_92-12200d others(98): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(249): Show |
2 | a0001c0003t0026g0054a0001c0003t0026g0354 | 2 | NA18955.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.92-12200_92-12199i others(258): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(89): Show |
1 | a0001c0001t0045g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.92-12328_92-12327i others(98): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | AGCCTCCC others(25): Show |
1 | a0001c0001t0014g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.92-12360_92-12359i others(34): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
A | G | 81 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(78): Show | 82 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.92-12373A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423667 | ||||||
| chr11:1423667
|
AGCCTCCC others(25): Show |
A | 16 | a0001c0001t0001g0034a0001c0001t0001g0150a0001c0001t0003g0263others(13): Show | 16 | HG00609.hp1 HG00639.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.92-12231_92-12200d others(34): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423667
|
AGCCTCCC others(57): Show |
A | 1 | a0001c0001t0009g0153 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.92-12263_92-12200d others(66): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423667 | |||||
| chr11:1423699
|
G | A | 1 | a0001c0001t0057g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.92-12341G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423699 | ||||||
| chr11:1423699
|
G | GGCCTCCC others(57): Show |
3 | a0001c0001t0001g0048a0001c0001t0043g0050a0002c0002t0002g0015 | 3 | HG02647.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.92-12328_92-12327i others(66): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423699 | |||||
| chr11:1423711
|
T | TGGGCGTT others(314): Show |
1 | a0001c0003t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.92-12200_92-12199i others(323): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423711 | |||||
| chr11:1423716
|
G | GTTCCGGG others(313): Show |
1 | a0001c0003t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.92-12264_92-12263i others(322): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423716 | |||||
| chr11:1423731
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0043g0050a0002c0002t0002g0015 | 3 | HG02647.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.92-12309G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423731 | ||||||
| chr11:1423763
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0043g0050a0002c0002t0002g0015 | 3 | HG02647.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.92-12277G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423763 | ||||||
| chr11:1423772
|
C | T | 9 | a0001c0001t0003g0288a0001c0001t0004g0190a0001c0001t0018g0137others(6): Show | 9 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-12268C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423772 | ||||||
| chr11:1423777
|
G | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0029 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.92-12263G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423777 | ||||||
| chr11:1423780
|
G | A | 17 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0127others(14): Show | 18 | HG00639.hp2 HG01192.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.92-12260G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423780 | ||||||
| chr11:1423804
|
C | A | 24 | a0001c0001t0001g0154a0001c0001t0001g0189a0001c0001t0001g0191others(21): Show | 24 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.92-12236C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423804 | ||||||
| chr11:1423826
|
A | AGGCCTCC others(345): Show |
2 | a0001c0001t0003g0002a0001c0001t0003g0203 | 3 | HG02723.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.92-12200_92-12199i others(354): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423826 | |||||
| chr11:1423826
|
A | AGGCCTCC others(313): Show |
1 | a0001c0001t0003g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92-12200_92-12199i others(322): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423826 | |||||
| chr11:1423826
|
A | AGGCCTCC others(377): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0029 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.92-12200_92-12199i others(386): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1423826 | |||||
| chr11:1423841
|
A | G | 4 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0099others(1): Show | 4 | NA18939.hp2 NA18940.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-12199A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1423841 | ||||||
| chr11:1424005
|
T | C | 201 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(198): Show | 203 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.92-12035T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424005 | ||||||
| chr11:1424123
|
T | C | 1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.92-11917T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424123 | ||||||
| chr11:1424132
|
A | G | 119 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(116): Show | 120 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.92-11908A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424132 | ||||||
| chr11:1424201
|
G | T | 1 | a0001c0001t0003g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.92-11839G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424201 | ||||||
| chr11:1424204
|
A | G | 1 | a0001c0001t0003g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.92-11836A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424204 | ||||||
| chr11:1424259
|
C | T | 1 | a0002c0002t0002g0014 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92-11781C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424259 | ||||||
| chr11:1424260
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92-11780G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424260 | ||||||
| chr11:1424267
|
G | A | 256 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(253): Show | 259 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.92-11773G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424267 | ||||||
| chr11:1424394
|
A | G | 2 | a0001c0003t0004g0290a0002c0002t0058g0325 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.92-11646A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424394 | ||||||
| chr11:1424453
|
A | G | 163 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(160): Show | 164 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.92-11587A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424453 | ||||||
| chr11:1424632
|
C | G | 1 | a0007c0013t0004g0065 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.92-11408C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424632 | ||||||
| chr11:1424736
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.92-11304T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424736 | ||||||
| chr11:1424737
|
C | CG | 105 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(102): Show | 106 | HG00280.hp2 HG00558.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.92-11296dupG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1424737 | |||||
| chr11:1424817
|
A | G | 109 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(106): Show | 110 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.92-11223A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424817 | ||||||
| chr11:1424823
|
G | T | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-11217G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424823 | ||||||
| chr11:1424834
|
T | A | 109 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(106): Show | 110 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.92-11206T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424834 | ||||||
| chr11:1424939
|
G | A | 3 | a0001c0001t0003g0194a0001c0001t0003g0196a0001c0001t0003g0237 | 3 | HG02559.hp1 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.92-11101G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424939 | ||||||
| chr11:1424978
|
C | T | 103 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(100): Show | 104 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.92-11062C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1424978 | ||||||
| chr11:1424980
|
C | CG | 5 | a0001c0001t0003g0263a0001c0001t0024g0299a0001c0003t0001g0146others(2): Show | 5 | HG01255.hp1 HG01515.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-11056dupG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1424980 | |||||
| chr11:1425006
|
C | A | 2 | a0001c0001t0001g0072a0002c0002t0008g0078 | 2 | HG01496.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.92-11034C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1425006 | ||||||
| chr11:1425074
|
T | C | 83 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(80): Show | 84 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.92-10966T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1425074 | ||||||
| chr11:1425093
|
G | A | 12 | a0001c0001t0001g0073a0001c0001t0004g0080a0001c0001t0004g0081others(9): Show | 12 | HG00438.hp2 HG02027.hp2 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.92-10947G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1425093 | ||||||
| chr11:1425125
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-10915C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1425125 | ||||||
| chr11:1425347
|
C | T | 78 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(75): Show | 79 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.92-10693C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1425347 | ||||||
| chr11:1425445
|
C | T | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.92-10595C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1425445 | ||||||
| chr11:1425446
|
G | A | 1 | a0002c0002t0002g0126 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.92-10594G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1425446 | ||||||
| chr11:1425463
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.92-10577C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1425463 | ||||||
| chr11:1425474
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-10566C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1425474 | ||||||
| chr11:1425665
|
C | G | 2 | a0001c0001t0001g0186a0003c0014t0002g0319 | 2 | NA19067.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.92-10375C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1425665 | ||||||
| chr11:1425682
|
G | A | 6 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(3): Show | 6 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-10358G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1425682 | ||||||
| chr11:1425710
|
C | T | 1 | a0001c0001t0006g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.92-10330C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1425710 | ||||||
| chr11:1425767
|
G | A | 1 | a0001c0001t0044g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.92-10273G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1425767 | ||||||
| chr11:1426071
|
G | GCCTGTGC others(10): Show |
1 | a0002c0002t0016g0208 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.92-9968_92-9952dup others(17): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1426071 | |||||
| chr11:1426217
|
TGGGGATG others(17): Show |
T | 153 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(150): Show | 153 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.92-9775_92-9752del others(24): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1426217 | |||||
| chr11:1426241
|
C | CGGGGATG others(89): Show |
1 | a0001c0001t0003g0002 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.92-9776_92-9775ins others(96): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1426241 | |||||
| chr11:1426241
|
CGGGGATG others(41): Show |
C | 3 | a0001c0001t0009g0068a0001c0001t0009g0100a0001c0001t0009g0101 | 3 | NA18966.hp1 NA18975.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.92-9775_92-9728del others(48): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1426241 | |||||
| chr11:1426437
|
C | T | 98 | a0001c0001t0001g0044a0001c0001t0001g0057a0001c0001t0001g0058others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.92-9603C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1426437 | ||||||
| chr11:1426453
|
C | T | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.92-9587C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1426453 | ||||||
| chr11:1426456
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.92-9584C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1426456 | ||||||
| chr11:1426716
|
T | G | 1 | a0001c0001t0001g0089 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.92-9324T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1426716 | ||||||
| chr11:1426778
|
C | T | 24 | a0001c0001t0001g0154a0001c0001t0001g0189a0001c0001t0001g0191others(21): Show | 24 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.92-9262C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1426778 | ||||||
| chr11:1426785
|
T | G | 1 | a0001c0001t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92-9255T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1426785 | ||||||
| chr11:1426850
|
A | T | 1 | a0001c0004t0001g0095 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.92-9190A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1426850 | ||||||
| chr11:1426851
|
G | T | 1 | a0001c0004t0001g0095 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.92-9189G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1426851 | ||||||
| chr11:1426889
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-9151C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1426889 | ||||||
| chr11:1426928
|
T | TG | 10 | a0001c0001t0001g0010a0001c0001t0004g0316a0001c0001t0018g0137others(7): Show | 10 | HG01081.hp2 HG01255.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-9105dupG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1426928 | |||||
| chr11:1426936
|
C | T | 24 | a0001c0001t0001g0154a0001c0001t0001g0189a0001c0001t0001g0191others(21): Show | 24 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.92-9104C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1426936 | ||||||
| chr11:1426937
|
G | A | 1 | a0001c0001t0003g0280 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.92-9103G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1426937 | ||||||
| chr11:1427009
|
G | A | 1 | a0002c0002t0002g0320 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.92-9031G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1427009 | ||||||
| chr11:1427011
|
G | A | 1 | a0001c0001t0004g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.92-9029G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1427011 | ||||||
| chr11:1427079
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92-8961G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1427079 | ||||||
| chr11:1427107
|
G | A | 27 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.92-8933G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1427107 | ||||||
| chr11:1427155
|
T | G | 2 | a0001c0001t0001g0067a0001c0001t0004g0084 | 2 | NA18947.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.92-8885T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1427155 | ||||||
| chr11:1427173
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-8867G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1427173 | ||||||
| chr11:1427445
|
C | T | 1 | a0002c0002t0002g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.92-8595C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1427445 | ||||||
| chr11:1427446
|
G | A | 1 | a0002c0002t0008g0181 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.92-8594G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1427446 | ||||||
| chr11:1427627
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0059g0041 | 3 | HG02055.hp2 HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.92-8413C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1427627 | ||||||
| chr11:1427873
|
C | T | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.92-8167C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1427873 | ||||||
| chr11:1427952
|
G | A | 1 | a0001c0001t0003g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.92-8088G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1427952 | ||||||
| chr11:1428051
|
C | A | 2 | a0001c0001t0001g0046a0001c0003t0003g0291 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.92-7989C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428051 | ||||||
| chr11:1428143
|
G | A | 45 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 46 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.92-7897G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428143 | ||||||
| chr11:1428146
|
C | T | 8 | a0001c0001t0001g0048a0001c0001t0001g0192a0001c0001t0014g0039others(5): Show | 8 | HG01192.hp1 HG02647.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-7894C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428146 | ||||||
| chr11:1428147
|
G | A | 2 | a0002c0008t0002g0326a0002c0008t0005g0278 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.92-7893G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428147 | ||||||
| chr11:1428176
|
G | A | 6 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(3): Show | 6 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-7864G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428176 | ||||||
| chr11:1428517
|
G | A | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.92-7523G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428517 | ||||||
| chr11:1428541
|
C | T | 4 | a0001c0001t0001g0048a0001c0001t0003g0228a0001c0001t0043g0050others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-7499C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428541 | ||||||
| chr11:1428591
|
A | G | 44 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(41): Show | 45 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.92-7449A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428591 | ||||||
| chr11:1428647
|
C | T | 2 | a0001c0001t0006g0214a0006c0012t0037g0293 | 2 | HG00323.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.92-7393C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428647 | ||||||
| chr11:1428669
|
G | T | 46 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0099others(43): Show | 48 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.92-7371G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428669 | ||||||
| chr11:1428765
|
A | T | 159 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(156): Show | 160 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.92-7275A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428765 | ||||||
| chr11:1428829
|
A | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.92-7211A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428829 | ||||||
| chr11:1428839
|
G | C | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92-7201G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428839 | ||||||
| chr11:1428948
|
T | C | 1 | a0007c0013t0004g0065 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.92-7092T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428948 | ||||||
| chr11:1428952
|
C | T | 3 | a0001c0001t0009g0068a0001c0001t0009g0100a0001c0001t0009g0101 | 3 | NA18966.hp1 NA18975.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.92-7088C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1428952 | ||||||
| chr11:1429001
|
T | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-7039T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429001 | ||||||
| chr11:1429025
|
C | T | 106 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(103): Show | 107 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.92-7015C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429025 | ||||||
| chr11:1429028
|
G | T | 2 | a0002c0002t0033g0286a0002c0002t0066g0285 | 2 | HG02738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.92-7012G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429028 | ||||||
| chr11:1429048
|
CAT | C | 3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92-6991_92-6990del others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429048 | ||||||
| chr11:1429091
|
C | T | 3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92-6949C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429091 | ||||||
| chr11:1429093
|
T | C | 158 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(155): Show | 159 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.92-6947T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429093 | ||||||
| chr11:1429094
|
G | A | 1 | a0002c0002t0002g0088 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.92-6946G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429094 | ||||||
| chr11:1429126
|
CTGGGTGT others(15): Show |
C | 1 | a0002c0002t0008g0078 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.92-6897_92-6876del others(22): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429126 | |||||
| chr11:1429205
|
G | A | 162 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(159): Show | 163 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.92-6835G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429205 | ||||||
| chr11:1429210
|
C | T | 2 | a0001c0001t0018g0334a0001c0001t0067g0252 | 2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.92-6830C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429210 | ||||||
| chr11:1429223
|
C | T | 3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92-6817C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429223 | ||||||
| chr11:1429235
|
GGTGTGTC others(88): Show |
G | 106 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(103): Show | 107 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.92-6793_92-6699del others(95): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429235 | |||||
| chr11:1429246
|
G | C | 1 | a0001c0001t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92-6794G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429246 | ||||||
| chr11:1429275
|
G | A | 1 | a0002c0002t0005g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.92-6765G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429275 | ||||||
| chr11:1429317
|
G | A | 9 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0024g0299others(6): Show | 10 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-6723G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429317 | ||||||
| chr11:1429322
|
C | T | 3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92-6718C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429322 | ||||||
| chr11:1429387
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-6653G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429387 | ||||||
| chr11:1429407
|
G | GGGTGTGC others(6): Show |
1 | a0001c0003t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.92-6632_92-6631ins others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429407 | |||||
| chr11:1429407
|
G | GGTGTGCA others(5): Show |
158 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(155): Show | 159 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.92-6625_92-6624ins others(12): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429407 | |||||
| chr11:1429407
|
G | GTGTGCAC others(4): Show |
3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92-6633_92-6632ins others(11): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429407 | ||||||
| chr11:1429456
|
A | C | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.92-6584A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429456 | ||||||
| chr11:1429465
|
T | C | 162 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(159): Show | 163 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.92-6575T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429465 | ||||||
| chr11:1429466
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-6574G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429466 | ||||||
| chr11:1429467
|
C | T | 2 | a0001c0001t0001g0046a0001c0003t0003g0291 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.92-6573C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429467 | ||||||
| chr11:1429468
|
G | A | 2 | a0001c0001t0001g0102a0002c0002t0002g0079 | 2 | NA19081.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.92-6572G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429468 | ||||||
| chr11:1429478
|
G | A | 3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92-6562G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429478 | ||||||
| chr11:1429511
|
C | G | 3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92-6529C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429511 | ||||||
| chr11:1429511
|
C | T | 2 | a0001c0003t0001g0115a0001c0003t0001g0146 | 2 | HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.92-6529C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429511 | ||||||
| chr11:1429523
|
G | GCTGTGCC others(40): Show |
2 | a0001c0001t0014g0039a0001c0001t0044g0016 | 2 | HG01192.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92-6500_92-6499ins others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429523 | |||||
| chr11:1429523
|
G | GCTGTGCC others(181): Show |
1 | a0001c0001t0045g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.92-6500_92-6499ins others(188): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429523 | |||||
| chr11:1429523
|
GCTGTGCC others(465): Show |
G | 2 | a0001c0001t0001g0191a0001c0001t0004g0185 | 2 | HG01069.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.92-6510_92-6039del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429523 | |||||
| chr11:1429523
|
GCTGTGCC others(1740): Show |
G | 1 | a0001c0001t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.92-6510_92-4764del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429523 | |||||
| chr11:1429523
|
GCTGTGCC others(1881): Show |
G | 2 | a0002c0005t0034g0055a0002c0005t0034g0056 | 2 | HG01346.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.92-6510_92-4623del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429523 | |||||
| chr11:1429523
|
GCTGTGCC others(2827): Show |
G | 3 | a0001c0001t0001g0059a0001c0001t0001g0130a0001c0001t0003g0268 | 3 | HG00621.hp1 HG01496.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.92-6322_92-3489del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429523 | |||||
| chr11:1429523
|
GCTGTGCC others(2874): Show |
G | 40 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0061others(37): Show | 40 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.92-6510_92-3630del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429523 | |||||
| chr11:1429523
|
GCTGTGCC others(2921): Show |
G | 10 | a0001c0001t0001g0082a0001c0001t0001g0097a0001c0001t0003g0194others(7): Show | 10 | HG00642.hp1 HG01081.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-6510_92-3583del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429523 | |||||
| chr11:1429523
|
GCTGTGCC others(2968): Show |
G | 4 | a0001c0001t0003g0002a0001c0001t0003g0045a0001c0001t0003g0196others(1): Show | 5 | HG02559.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-6510_92-3536del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429523 | |||||
| chr11:1429523
|
GCTGTGCC others(3438): Show |
G | 13 | a0002c0002t0002g0013a0002c0002t0002g0014a0002c0002t0002g0018others(10): Show | 13 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-6510_92-3066del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429523 | |||||
| chr11:1429523
|
GCTGTGCC others(3485): Show |
G | 1 | a0002c0017t0052g0008 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.92-6510_92-3019del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429523 | |||||
| chr11:1429530
|
C | T | 80 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0066others(77): Show | 80 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.92-6510C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429530 | ||||||
| chr11:1429530
|
CCAGCAGT others(87): Show |
C | 1 | a0002c0002t0020g0148 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.92-6158_92-6065del others(94): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429530 | |||||
| chr11:1429530
|
CCAGCAGT others(700): Show |
C | 1 | a0002c0002t0002g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92-6416_92-5710del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429530 | |||||
| chr11:1429530
|
CCAGCAGT others(2921): Show |
C | 2 | a0001c0001t0001g0343a0001c0001t0047g0340 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.92-6416_92-3489del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429530 | |||||
| chr11:1429541
|
CGTCTTCT others(1922): Show |
C | 1 | a0001c0003t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.92-6496_92-4568del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429541 | |||||
| chr11:1429550
|
CGGTCTGG others(418): Show |
C | 3 | a0001c0001t0004g0190a0001c0001t0048g0342a0001c0001t0057g0184 | 3 | HG02738.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.92-6369_92-5945del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429550 | |||||
| chr11:1429551
|
G | A | 9 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0089others(6): Show | 9 | HG00438.hp2 HG01981.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.92-6489G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429551 | ||||||
| chr11:1429577
|
T | C | 8 | a0001c0001t0001g0048a0001c0001t0001g0192a0001c0001t0014g0039others(5): Show | 8 | HG01192.hp1 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-6463T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429577 | ||||||
| chr11:1429577
|
TCAGCAGT others(2686): Show |
T | 1 | a0001c0001t0001g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.92-6416_92-3724del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429577 | |||||
| chr11:1429577
|
TCAGCAGT others(2733): Show |
T | 1 | a0001c0001t0001g0102 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.92-6416_92-3677del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429577 | |||||
| chr11:1429577
|
TCAGCAGT others(2780): Show |
T | 3 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0073 | 3 | HG00438.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.92-6275_92-3489del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429577 | |||||
| chr11:1429577
|
TCAGCAGT others(3015): Show |
T | 1 | a0001c0001t0003g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.92-6416_92-3395del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429577 | |||||
| chr11:1429577
|
TCAGCAGT others(3203): Show |
T | 1 | a0001c0003t0001g0135 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.92-6416_92-3207del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429577 | |||||
| chr11:1429580
|
G | GCAGTGAG others(40): Show |
2 | a0002c0007t0010g0244a0002c0007t0010g0245 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.92-6414_92-6413ins others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429580 | |||||
| chr11:1429597
|
CGGTCTGG others(2639): Show |
C | 1 | a0001c0001t0006g0248 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.92-6416_92-3771del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429597 | |||||
| chr11:1429624
|
T | C | 33 | a0001c0001t0001g0048a0001c0001t0001g0192a0001c0001t0004g0175others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.92-6416T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429624 | ||||||
| chr11:1429624
|
T | TCAGCAGT others(326): Show |
1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92-6394_92-6393ins others(333): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429624 | |||||
| chr11:1429624
|
TCAGCAGT others(2639): Show |
T | 1 | a0001c0001t0003g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.92-6369_92-3724del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429624 | |||||
| chr11:1429624
|
TCAGCAGT others(2733): Show |
T | 17 | a0001c0001t0001g0113a0001c0001t0001g0339a0001c0001t0003g0193others(14): Show | 17 | HG00280.hp2 HG01257.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.92-6228_92-3489del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429624 | |||||
| chr11:1429624
|
TCAGCAGT others(2921): Show |
T | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.92-6369_92-3442del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429624 | |||||
| chr11:1429624
|
TCAGCAGT others(2968): Show |
T | 3 | a0001c0001t0001g0312a0001c0001t0003g0234a0002c0005t0005g0289 | 3 | HG02818.hp2 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.92-6369_92-3395del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429624 | |||||
| chr11:1429624
|
TCAGCAGT others(3015): Show |
T | 1 | a0001c0001t0003g0238 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.92-6369_92-3348del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429624 | |||||
| chr11:1429644
|
C | T | 8 | a0001c0001t0001g0087a0001c0001t0001g0107a0001c0001t0006g0197others(5): Show | 9 | HG00280.hp1 HG00609.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.92-6396C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429644 | ||||||
| chr11:1429644
|
CGGTCTGG others(1127): Show |
C | 3 | a0001c0001t0004g0175a0001c0001t0004g0180a0001c0016t0018g0183 | 3 | HG01993.hp2 HG02273.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.92-6369_92-5236del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429644 | |||||
| chr11:1429644
|
CGGTCTGG others(2592): Show |
C | 7 | a0001c0001t0004g0172a0001c0001t0004g0314a0001c0001t0004g0316others(4): Show | 7 | HG01943.hp1 HG01975.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-6369_92-3771del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429644 | |||||
| chr11:1429645
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0011g0295 | 2 | NA18952.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.92-6395G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429645 | ||||||
| chr11:1429671
|
T | C | 39 | a0001c0001t0001g0048a0001c0001t0001g0066a0001c0001t0001g0189others(36): Show | 39 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.92-6369T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429671 | ||||||
| chr11:1429671
|
TCAGCAGT others(2592): Show |
T | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.92-6322_92-3724del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429671 | |||||
| chr11:1429691
|
CGGTCTGG others(1080): Show |
C | 4 | a0001c0001t0004g0161a0001c0001t0004g0179a0001c0001t0006g0215others(1): Show | 4 | HG00639.hp2 HG01261.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-6322_92-5236del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429691 | |||||
| chr11:1429691
|
CGGTCTGG others(2214): Show |
C | 1 | a0001c0001t0001g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.92-6322_92-4102del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429691 | |||||
| chr11:1429704
|
TTTTGCCA others(417): Show |
T | 1 | a0001c0001t0068g0243 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.92-6332_92-5909del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429704 | |||||
| chr11:1429718
|
T | C | 7 | a0001c0001t0001g0048a0001c0001t0003g0228a0001c0001t0004g0177others(4): Show | 7 | HG01192.hp1 HG01192.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-6322T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429718 | ||||||
| chr11:1429718
|
TCAGCAGT others(2639): Show |
T | 2 | a0001c0001t0001g0089a0001c0001t0011g0295 | 2 | NA18952.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.92-6134_92-3489del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429718 | |||||
| chr11:1429718
|
TCAGCAGT others(2921): Show |
T | 1 | a0001c0001t0006g0247 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.92-6275_92-3348del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429718 | |||||
| chr11:1429738
|
CGGTCTGG others(2167): Show |
C | 1 | a0001c0001t0004g0177 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.92-6275_92-4102del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429738 | |||||
| chr11:1429765
|
T | C | 7 | a0001c0001t0001g0048a0001c0001t0001g0192a0001c0001t0003g0228others(4): Show | 7 | HG01192.hp1 HG02145.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-6275T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429765 | ||||||
| chr11:1429787
|
GTCTGGTC others(3342): Show |
G | 4 | a0001c0003t0014g0036a0001c0003t0014g0037a0001c0003t0014g0038others(1): Show | 4 | HG00642.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-6252_92-2904del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429787 | ||||||
| chr11:1429792
|
G | A | 1 | a0002c0002t0020g0148 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.92-6248G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429792 | ||||||
| chr11:1429812
|
T | C | 7 | a0001c0001t0001g0048a0001c0001t0001g0066a0001c0001t0014g0039others(4): Show | 7 | HG01192.hp1 HG01981.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-6228T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429812 | ||||||
| chr11:1429834
|
GTCTGGTC others(1879): Show |
G | 1 | a0001c0003t0001g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.92-6205_92-4320del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429834 | ||||||
| chr11:1429859
|
T | C | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-6181T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429859 | ||||||
| chr11:1429859
|
TCAGCAGT others(1033): Show |
T | 6 | a0001c0001t0001g0313a0002c0002t0007g0294a0002c0002t0007g0304others(3): Show | 6 | HG01952.hp2 HG01975.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-6064_92-5025del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429859 | |||||
| chr11:1429881
|
GTCTGGTC others(604): Show |
G | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.92-6158_92-5548del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429881 | ||||||
| chr11:1429881
|
GTCTGGTC others(3201): Show |
G | 19 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0134others(16): Show | 19 | HG00423.hp1 HG00558.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.92-6158_92-2951del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429881 | ||||||
| chr11:1429886
|
G | A | 1 | a0002c0002t0005g0258 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.92-6154G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429886 | ||||||
| chr11:1429906
|
T | C | 5 | a0001c0001t0001g0048a0001c0001t0014g0039a0001c0001t0043g0050others(2): Show | 5 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-6134T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429906 | ||||||
| chr11:1429906
|
TCAGCAGT others(986): Show |
T | 30 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0123others(27): Show | 31 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.92-6064_92-5072del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429906 | |||||
| chr11:1429926
|
CGGTCTGG others(42): Show |
C | 17 | a0001c0001t0064g0261a0001c0001t0076g0182a0002c0002t0002g0098others(14): Show | 17 | HG00544.hp2 HG01099.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.92-6064_92-6016del others(49): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429926 | |||||
| chr11:1429926
|
CGGTCTGG others(1836): Show |
C | 1 | a0002c0002t0005g0258 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.92-6064_92-4222del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429926 | |||||
| chr11:1429933
|
G | A | 20 | a0001c0001t0001g0099a0001c0001t0009g0153a0001c0001t0009g0187others(17): Show | 20 | HG00140.hp1 HG00408.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-6107G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429933 | ||||||
| chr11:1429953
|
T | C | 6 | a0001c0001t0001g0048a0001c0001t0001g0192a0001c0001t0014g0039others(3): Show | 6 | HG01192.hp1 HG02647.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-6087T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429953 | ||||||
| chr11:1429953
|
T | TCAGCAGT others(136): Show |
1 | a0001c0001t0078g0205 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.92-6065_92-6064ins others(143): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429953 | |||||
| chr11:1429953
|
TCAGCAGT others(136): Show |
T | 5 | a0001c0001t0009g0153a0001c0001t0018g0334a0001c0001t0067g0252others(2): Show | 5 | HG00408.hp2 HG03942.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-6064_92-5922del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429953 | |||||
| chr11:1429953
|
TCAGCAGT others(939): Show |
T | 5 | a0002c0002t0002g0132a0002c0002t0017g0301a0002c0002t0022g0003others(2): Show | 6 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-6064_92-5119del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429953 | |||||
| chr11:1429973
|
CGG | C | 105 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.92-6064_92-6063del others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429973 | |||||
| chr11:1429973
|
CGGGGTCT others(655): Show |
C | 1 | a0002c0002t0020g0125 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.92-6064_92-5403del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429973 | |||||
| chr11:1429975
|
G | GTCTGGTC others(38): Show |
1 | a0001c0001t0006g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.92-6065_92-6064ins others(45): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429975 | ||||||
| chr11:1429975
|
G | GTCTGGTC others(85): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0107 | 2 | HG00280.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.92-6065_92-6064ins others(92): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429975 | ||||||
| chr11:1429975
|
GGGTCTGG others(40): Show |
G | 1 | a0002c0002t0002g0086 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.92-5991_92-5945del others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1429975 | |||||
| chr11:1429982
|
G | A | 13 | a0001c0001t0006g0214a0002c0002t0002g0098a0002c0002t0002g0164others(10): Show | 13 | HG00323.hp1 HG00544.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.92-6058G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1429982 | ||||||
| chr11:1430002
|
T | C | 8 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0192others(5): Show | 8 | HG01192.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-6038T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430002 | ||||||
| chr11:1430049
|
T | C | 11 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0003g0228others(8): Show | 11 | HG01192.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-5991T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430049 | ||||||
| chr11:1430049
|
TCAGCAGT others(416): Show |
T | 1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.92-5897_92-5475del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430049 | |||||
| chr11:1430049
|
TCAGCAGT others(2214): Show |
T | 1 | a0002c0002t0005g0277 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.92-5474_92-3254del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430049 | |||||
| chr11:1430069
|
C | CGG | 7 | a0001c0001t0001g0023a0001c0001t0001g0066a0001c0001t0001g0087others(4): Show | 7 | HG00280.hp1 HG01884.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-5970_92-5969dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430069 | |||||
| chr11:1430071
|
GTCTGGTC others(273): Show |
G | 1 | a0002c0002t0002g0158 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.92-5968_92-5689del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430071 | ||||||
| chr11:1430081
|
GTTTTGCC others(512): Show |
G | 1 | a0002c0002t0007g0345 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.92-5956_92-5438del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430081 | |||||
| chr11:1430096
|
C | T | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(97): Show | 101 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.92-5944C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430096 | ||||||
| chr11:1430116
|
C | CGG | 12 | a0001c0001t0001g0168a0001c0001t0003g0241a0001c0001t0004g0121others(9): Show | 12 | HG00735.hp1 HG01257.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.92-5923_92-5922dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430116 | |||||
| chr11:1430116
|
C | CGGTCTGG others(91): Show |
4 | a0001c0001t0001g0034a0001c0001t0003g0220a0001c0001t0004g0136others(1): Show | 4 | HG00140.hp2 HG01516.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-5875_92-5874ins others(98): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430116 | |||||
| chr11:1430116
|
C | CGGTCTGG others(42): Show |
6 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0004g0051others(3): Show | 6 | HG00673.hp2 HG01243.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-5898_92-5897ins others(49): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430116 | |||||
| chr11:1430118
|
GTCTGGTC others(557): Show |
G | 1 | a0002c0002t0007g0306 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.92-5921_92-5358del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430118 | ||||||
| chr11:1430118
|
GTCTGGTC others(604): Show |
G | 10 | a0001c0001t0001g0099a0001c0001t0009g0187a0001c0001t0011g0310others(7): Show | 10 | HG00140.hp1 HG01255.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-5921_92-5311del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430118 | ||||||
| chr11:1430118
|
GTCTGGTC others(888): Show |
G | 1 | a0002c0002t0002g0152 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.92-5921_92-5027del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430118 | ||||||
| chr11:1430118
|
GTCTGGTC others(935): Show |
G | 2 | a0001c0001t0024g0299a0002c0002t0002g0119 | 2 | HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.92-5921_92-4980del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430118 | ||||||
| chr11:1430118
|
GTCTGGTC others(2588): Show |
G | 1 | a0001c0001t0003g0227 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.92-5921_92-3327del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430118 | ||||||
| chr11:1430143
|
C | T | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 63 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.92-5897C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430143 | ||||||
| chr11:1430143
|
CCAGCAGT others(40): Show |
C | 2 | a0001c0001t0003g0222a0001c0001t0003g0270 | 2 | NA18945.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.92-5756_92-5710del others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430143 | |||||
| chr11:1430163
|
C | CGG | 25 | a0001c0001t0001g0049a0001c0001t0001g0168a0001c0001t0001g0186others(22): Show | 25 | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.92-5876_92-5875dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430163 | |||||
| chr11:1430163
|
C | CGGGGTCT others(44): Show |
16 | a0001c0001t0001g0030a0001c0001t0001g0052a0001c0001t0001g0053others(13): Show | 17 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-5875_92-5874ins others(51): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430163 | |||||
| chr11:1430163
|
C | CGGTCTGG others(91): Show |
7 | a0001c0001t0001g0141a0001c0001t0013g0022a0002c0002t0016g0284others(4): Show | 7 | HG01167.hp2 HG01891.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-5851_92-5850ins others(98): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430163 | |||||
| chr11:1430163
|
C | G | 1 | a0001c0001t0059g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-5877C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430163 | ||||||
| chr11:1430165
|
GTCTGGTC others(38): Show |
G | 11 | a0002c0002t0002g0098a0002c0002t0002g0164a0002c0002t0002g0166others(8): Show | 11 | HG00544.hp2 HG01099.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.92-5874_92-5830del others(45): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430165 | ||||||
| chr11:1430165
|
GTCTGGTC others(557): Show |
G | 2 | a0001c0001t0006g0214a0002c0002t0005g0216 | 2 | HG00323.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.92-5874_92-5311del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430165 | ||||||
| chr11:1430190
|
T | C | 73 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 74 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.92-5850T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430190 | ||||||
| chr11:1430190
|
T | TCAGCAGT others(42): Show |
1 | a0002c0002t0010g0004 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.92-5828_92-5827ins others(49): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430190 | |||||
| chr11:1430190
|
T | TCAGCAGT others(91): Show |
1 | a0002c0002t0010g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.92-5828_92-5827ins others(98): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430190 | |||||
| chr11:1430202
|
GTCTTCTG others(2872): Show |
G | 1 | a0001c0001t0001g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.92-5758_92-2880del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430202 | |||||
| chr11:1430210
|
C | CGG | 20 | a0001c0001t0001g0186a0001c0001t0001g0192a0001c0001t0003g0219others(17): Show | 21 | HG00639.hp1 HG01099.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.92-5829_92-5828dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430210 | |||||
| chr11:1430210
|
C | CGGGGTCT others(44): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02055.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.92-5828_92-5827ins others(51): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430210 | |||||
| chr11:1430210
|
C | CGGTCTGG others(91): Show |
1 | a0001c0001t0001g0127 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.92-5804_92-5803ins others(98): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430210 | |||||
| chr11:1430212
|
GTCTGGTC others(38): Show |
G | 1 | a0001c0001t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92-5827_92-5783del others(45): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430212 | ||||||
| chr11:1430237
|
T | C | 85 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0023others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.92-5803T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430237 | ||||||
| chr11:1430257
|
C | CGG | 8 | a0001c0001t0001g0192a0001c0001t0009g0153a0001c0001t0018g0334others(5): Show | 8 | HG00408.hp2 HG01099.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-5782_92-5781dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430257 | |||||
| chr11:1430257
|
C | CGGTCTGG others(42): Show |
1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92-5782_92-5734dup others(49): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430257 | |||||
| chr11:1430279
|
T | TGTGCCCA others(40): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02055.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.92-5757_92-5756ins others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430279 | |||||
| chr11:1430284
|
T | C | 92 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(89): Show | 95 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.92-5756T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430284 | ||||||
| chr11:1430284
|
TCAGCAGT others(845): Show |
T | 2 | a0002c0002t0005g0262a0002c0002t0041g0144 | 2 | NA18967.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.92-5615_92-4764del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430284 | |||||
| chr11:1430284
|
TCAGCAGT others(1268): Show |
T | 2 | a0002c0002t0002g0320a0002c0002t0005g0274 | 2 | HG02080.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.92-5615_92-4341del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430284 | |||||
| chr11:1430304
|
CGGTCTGG others(798): Show |
C | 2 | a0001c0001t0018g0334a0001c0001t0067g0252 | 2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.92-5568_92-4764del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430304 | |||||
| chr11:1430331
|
C | T | 15 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0003g0239others(12): Show | 15 | HG00408.hp2 HG00609.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.92-5709C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430331 | ||||||
| chr11:1430353
|
GTCTGGTC others(796): Show |
G | 1 | a0002c0002t0058g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-5686_92-4884del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430353 | ||||||
| chr11:1430373
|
T | C | 1 | a0007c0013t0004g0065 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.92-5667T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430373 | ||||||
| chr11:1430378
|
C | T | 16 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0087others(13): Show | 16 | HG00280.hp1 HG00639.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.92-5662C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430378 | ||||||
| chr11:1430378
|
CCAGCAGT others(1033): Show |
C | 1 | a0002c0002t0050g0165 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.92-5474_92-4435del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430378 | |||||
| chr11:1430395
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92-5645C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430395 | ||||||
| chr11:1430398
|
C | CGGGGTCT others(140): Show |
1 | a0001c0001t0078g0205 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.92-5640_92-5639ins others(147): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430398 | |||||
| chr11:1430398
|
CGGTCTGG others(230): Show |
C | 6 | a0002c0002t0002g0098a0002c0002t0002g0164a0002c0002t0002g0166others(3): Show | 6 | HG00544.hp2 HG02040.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-5615_92-5379del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430398 | |||||
| chr11:1430425
|
C | T | 45 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0030others(42): Show | 45 | HG00323.hp2 HG00673.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.92-5615C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430425 | ||||||
| chr11:1430472
|
C | T | 53 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0023others(50): Show | 54 | HG00323.hp2 HG00408.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.92-5568C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430472 | ||||||
| chr11:1430472
|
CCAGCAGT others(87): Show |
C | 1 | a0002c0002t0005g0269 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.92-5521_92-5428del others(94): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430472 | |||||
| chr11:1430472
|
CCAGCAGT others(939): Show |
C | 1 | a0001c0001t0057g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.92-5474_92-4529del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430472 | |||||
| chr11:1430492
|
CGGTCTGG others(610): Show |
C | 1 | a0001c0001t0004g0185 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.92-5474_92-4858del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430492 | |||||
| chr11:1430512
|
A | G | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.92-5528A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430512 | ||||||
| chr11:1430519
|
C | CCAGCAGT others(42): Show |
8 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0004g0051others(5): Show | 8 | HG00673.hp2 HG01243.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-5499_92-5498ins others(49): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430519 | |||||
| chr11:1430519
|
C | T | 26 | a0001c0001t0001g0023a0001c0001t0001g0087a0001c0001t0001g0107others(23): Show | 28 | HG00280.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.92-5521C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430519 | ||||||
| chr11:1430519
|
CCAGCAGT others(420): Show |
C | 3 | a0001c0001t0009g0153a0002c0002t0008g0151a0005c0010t0002g0085 | 3 | HG00408.hp2 NA18612.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.92-5404_92-4978del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430519 | |||||
| chr11:1430519
|
CCAGCAGT others(845): Show |
C | 1 | a0001c0001t0001g0048 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.92-5427_92-4576del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430519 | |||||
| chr11:1430539
|
C | CGG | 5 | a0001c0001t0001g0023a0001c0001t0006g0197a0001c0001t0006g0226others(2): Show | 5 | HG00735.hp1 HG00738.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-5500_92-5499dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430539 | |||||
| chr11:1430539
|
CGGTCTGG others(89): Show |
C | 3 | a0002c0002t0002g0158a0002c0002t0002g0169a0002c0002t0002g0170 | 3 | HG01099.hp2 HG01515.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.92-5404_92-5309del others(96): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430539 | |||||
| chr11:1430539
|
CGGTCTGG others(1697): Show |
C | 4 | a0001c0001t0001g0191a0001c0001t0004g0190a0001c0001t0048g0342others(1): Show | 4 | HG01255.hp2 HG01891.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-5474_92-3771del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430539 | |||||
| chr11:1430544
|
T | C | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92-5496T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430544 | ||||||
| chr11:1430566
|
T | C | 44 | a0001c0001t0001g0049a0001c0001t0001g0127a0001c0001t0001g0141others(41): Show | 46 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.92-5474T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430566 | ||||||
| chr11:1430586
|
C | CGG | 37 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0030others(34): Show | 37 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.92-5453_92-5452dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430586 | |||||
| chr11:1430586
|
C | CGGGGTCT others(44): Show |
1 | a0001c0001t0001g0317 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.92-5452_92-5451ins others(51): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430586 | |||||
| chr11:1430586
|
C | CGGTCTGG others(88): Show |
1 | a0001c0001t0003g0219 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.92-5428_92-5427ins others(95): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430586 | |||||
| chr11:1430586
|
CGGTCTGG others(185): Show |
C | 1 | a0001c0001t0043g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.92-5427_92-5236del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430586 | |||||
| chr11:1430591
|
T | C | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92-5449T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430591 | ||||||
| chr11:1430609
|
G | C | 1 | a0002c0002t0007g0345 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.92-5431G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430609 | ||||||
| chr11:1430613
|
T | C | 19 | a0001c0001t0001g0049a0001c0001t0001g0127a0001c0001t0014g0039others(16): Show | 20 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-5427T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430613 | ||||||
| chr11:1430633
|
CGG | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0192a0001c0001t0003g0239others(15): Show | 18 | HG00438.hp1 HG00609.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.92-5404_92-5403del others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430633 | |||||
| chr11:1430635
|
G | GGGTCTGG others(87): Show |
3 | a0001c0001t0003g0200a0001c0001t0003g0201a0002c0002t0008g0071 | 3 | HG00673.hp2 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.92-5379_92-5378ins others(94): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430635 | |||||
| chr11:1430635
|
G | GGGTCTGG others(228): Show |
1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92-5332_92-5331ins others(235): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430635 | |||||
| chr11:1430635
|
G | GTCTGGTC others(134): Show |
1 | a0006c0012t0037g0293 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.92-5405_92-5404ins others(141): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430635 | ||||||
| chr11:1430635
|
G | GTCTGGTC others(326): Show |
1 | a0001c0001t0001g0127 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.92-5405_92-5404ins others(333): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430635 | ||||||
| chr11:1430635
|
G | GTCTGGTC others(181): Show |
1 | a0007c0013t0004g0065 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.92-5405_92-5404ins others(188): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430635 | ||||||
| chr11:1430635
|
GGGTCTGG others(230): Show |
G | 3 | a0002c0002t0002g0075a0002c0002t0002g0086a0002c0002t0005g0005 | 4 | NA18995.hp2 NA18999.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-5378_92-5142del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430635 | |||||
| chr11:1430662
|
T | C | 17 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0107others(14): Show | 17 | HG00280.hp1 HG00735.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-5378T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430662 | ||||||
| chr11:1430662
|
T | TCAGCAGT others(40): Show |
1 | a0001c0001t0063g0253 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.92-5332_92-5331ins others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430662 | |||||
| chr11:1430682
|
C | CGG | 20 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0141others(17): Show | 21 | HG00140.hp2 HG01167.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.92-5357_92-5356dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430682 | |||||
| chr11:1430684
|
GTCTGGTC others(228): Show |
G | 1 | a0002c0002t0019g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.92-5355_92-5121del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430684 | ||||||
| chr11:1430684
|
GTCTGGTC others(275): Show |
G | 1 | a0002c0002t0033g0279 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.92-5355_92-5074del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430684 | ||||||
| chr11:1430709
|
T | C | 10 | a0001c0001t0001g0023a0001c0001t0001g0192a0001c0001t0003g0228others(7): Show | 10 | HG00639.hp1 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-5331T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430709 | ||||||
| chr11:1430729
|
C | CGG | 33 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 33 | HG00323.hp2 HG00741.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.92-5310_92-5309dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430729 | |||||
| chr11:1430729
|
C | CGGTCTGG others(330): Show |
1 | a0001c0001t0044g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.92-5285_92-5284ins others(337): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430729 | |||||
| chr11:1430742
|
TTTTGCCA others(513): Show |
T | 1 | a0002c0002t0007g0345 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.92-5294_92-4775del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430742 | |||||
| chr11:1430756
|
T | C | 21 | a0001c0001t0001g0023a0001c0001t0001g0127a0001c0001t0003g0200others(18): Show | 21 | HG00639.hp1 HG00673.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.92-5284T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430756 | ||||||
| chr11:1430756
|
T | TCAGCAGT others(42): Show |
5 | a0001c0001t0001g0168a0001c0001t0004g0121a0001c0001t0025g0143others(2): Show | 5 | HG01167.hp2 HG01891.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-5261_92-5213dup others(49): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430756 | |||||
| chr11:1430756
|
T | TCAGCAGT others(87): Show |
2 | a0002c0007t0010g0244a0002c0007t0010g0245 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.92-5262_92-5261ins others(94): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430756 | |||||
| chr11:1430776
|
CGG | C | 32 | a0001c0001t0001g0023a0001c0001t0001g0099a0001c0001t0001g0192others(29): Show | 32 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.92-5261_92-5260del others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430776 | |||||
| chr11:1430776
|
CGGGGTCT others(326): Show |
C | 1 | a0002c0002t0002g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.92-5261_92-4929del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430776 | |||||
| chr11:1430778
|
G | GTCTGGTC others(38): Show |
1 | a0002c0002t0010g0233 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.92-5262_92-5261ins others(45): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430778 | ||||||
| chr11:1430778
|
G | GTCTGGTC others(134): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0107 | 2 | HG00280.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.92-5262_92-5261ins others(141): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430778 | ||||||
| chr11:1430805
|
C | T | 26 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0099others(23): Show | 27 | HG00140.hp1 HG00735.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.92-5235C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430805 | ||||||
| chr11:1430825
|
C | CGG | 18 | a0001c0001t0001g0141a0001c0001t0001g0186a0001c0001t0004g0136others(15): Show | 19 | HG00140.hp2 HG00639.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.92-5214_92-5213dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430825 | |||||
| chr11:1430827
|
GTCTGGTC others(1266): Show |
G | 1 | a0001c0001t0003g0222 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.92-5212_92-3940del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430827 | ||||||
| chr11:1430852
|
C | T | 22 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0049others(19): Show | 23 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.92-5188C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430852 | ||||||
| chr11:1430852
|
CCAGCAGT others(87): Show |
C | 1 | a0002c0002t0008g0181 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.92-5141_92-5048del others(94): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430852 | |||||
| chr11:1430872
|
C | CGG | 6 | a0001c0001t0001g0009a0001c0001t0001g0192a0001c0001t0004g0051others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-5167_92-5166dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430872 | |||||
| chr11:1430872
|
C | CGGGGTCT others(238): Show |
1 | a0001c0001t0045g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.92-5166_92-5165ins others(245): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430872 | |||||
| chr11:1430874
|
GTCTGGTC others(132): Show |
G | 1 | a0001c0001t0076g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.92-5165_92-5027del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430874 | ||||||
| chr11:1430899
|
C | T | 53 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 54 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.92-5141C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430899 | ||||||
| chr11:1430899
|
CCAGCAGT others(371): Show |
C | 3 | a0001c0001t0001g0099a0001c0001t0009g0187a0002c0002t0002g0155 | 3 | NA18944.hp1 NA18964.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.92-4953_92-4576del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430899 | |||||
| chr11:1430926
|
G | A | 19 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0123others(16): Show | 20 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-5114G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430926 | ||||||
| chr11:1430946
|
T | C | 38 | a0001c0001t0001g0009a0001c0001t0001g0127a0001c0001t0003g0200others(35): Show | 38 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.92-5094T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430946 | ||||||
| chr11:1430946
|
TCAGCAGT others(1080): Show |
T | 1 | a0002c0002t0005g0269 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.92-4930_92-3844del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430946 | |||||
| chr11:1430966
|
C | CGG | 5 | a0001c0001t0003g0239a0002c0002t0002g0169a0002c0002t0002g0170others(2): Show | 5 | HG00741.hp2 HG01099.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-5073_92-5072dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430966 | |||||
| chr11:1430966
|
C | CGGTCTGG others(334): Show |
1 | a0001c0001t0014g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.92-5048_92-5047ins others(341): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1430966 | |||||
| chr11:1430993
|
T | C | 48 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0049others(45): Show | 49 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.92-5047T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1430993 | ||||||
| chr11:1431013
|
C | CGG | 15 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0027g0129others(12): Show | 16 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.92-5026_92-5025dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431013 | |||||
| chr11:1431040
|
T | C | 54 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0052others(51): Show | 55 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.92-5000T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431040 | ||||||
| chr11:1431060
|
C | CGG | 6 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0031g0012others(3): Show | 6 | HG01099.hp1 HG01943.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-4979_92-4978dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431060 | |||||
| chr11:1431060
|
CGGTCTGG others(42): Show |
C | 7 | a0001c0001t0006g0214a0001c0001t0011g0310a0002c0002t0007g0306others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-4953_92-4905del others(49): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431060 | |||||
| chr11:1431087
|
T | C | 90 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0023others(87): Show | 91 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.92-4953T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431087 | ||||||
| chr11:1431087
|
T | TCAGCAGT others(40): Show |
2 | a0001c0001t0004g0121a0001c0001t0025g0143 | 2 | HG02129.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.92-4931_92-4930ins others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431087 | |||||
| chr11:1431107
|
CGG | C | 63 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0049others(60): Show | 65 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.92-4930_92-4929del others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431107 | |||||
| chr11:1431109
|
G | GTCTGGTC others(38): Show |
2 | a0001c0001t0027g0129a0006c0012t0037g0293 | 2 | HG00738.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.92-4931_92-4930ins others(45): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431109 | ||||||
| chr11:1431109
|
G | GTCTGGTC others(87): Show |
1 | a0001c0001t0001g0168 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.92-4931_92-4930ins others(94): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431109 | ||||||
| chr11:1431109
|
G | GTCTGGTC others(85): Show |
1 | a0002c0002t0008g0071 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.92-4931_92-4930ins others(92): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431109 | ||||||
| chr11:1431109
|
G | GTCTGGTC others(179): Show |
1 | a0002c0002t0008g0116 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.92-4931_92-4930ins others(186): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431109 | ||||||
| chr11:1431109
|
GGGTCTGG others(40): Show |
G | 1 | a0002c0002t0019g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.92-4810_92-4764del others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431109 | |||||
| chr11:1431109
|
GGGTCTGG others(134): Show |
G | 5 | a0002c0002t0002g0098a0002c0002t0002g0164a0002c0002t0002g0166others(2): Show | 5 | HG00544.hp2 HG02040.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-4904_92-4764del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431109 | |||||
| chr11:1431136
|
C | T | 52 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0069others(49): Show | 54 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.92-4904C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431136 | ||||||
| chr11:1431147
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.92-4893C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431147 | ||||||
| chr11:1431156
|
C | CGG | 11 | a0001c0001t0001g0072a0001c0001t0001g0123a0001c0001t0001g0124others(8): Show | 12 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.92-4883_92-4882dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431156 | |||||
| chr11:1431156
|
CGGTCTGG others(1080): Show |
C | 1 | a0001c0001t0003g0270 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.92-4763_92-3677del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431156 | |||||
| chr11:1431158
|
GTCTGGTC others(38): Show |
G | 2 | a0001c0001t0001g0186a0002c0002t0019g0042 | 2 | HG03540.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.92-4881_92-4837del others(45): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431158 | ||||||
| chr11:1431158
|
GTCTGGTC others(85): Show |
G | 1 | a0002c0002t0022g0204 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.92-4881_92-4790del others(92): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431158 | ||||||
| chr11:1431158
|
GTCTGGTC others(794): Show |
G | 1 | a0002c0002t0020g0148 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.92-4881_92-4081del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431158 | ||||||
| chr11:1431183
|
C | T | 46 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0063others(43): Show | 48 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.92-4857C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431183 | ||||||
| chr11:1431183
|
CCAGCAGT others(87): Show |
C | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.92-4810_92-4717del others(94): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431183 | |||||
| chr11:1431183
|
CCAGCAGT others(228): Show |
C | 1 | a0002c0002t0002g0159 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.92-4763_92-4529del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431183 | |||||
| chr11:1431195
|
G | A | 1 | a0001c0001t0043g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.92-4845G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431195 | ||||||
| chr11:1431205
|
GTCTGGTC others(38): Show |
G | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-4834_92-4790del others(45): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431205 | ||||||
| chr11:1431230
|
C | T | 21 | a0001c0001t0001g0009a0001c0001t0001g0049a0001c0001t0001g0052others(18): Show | 22 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.92-4810C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431230 | ||||||
| chr11:1431230
|
CCAGCAGT others(40): Show |
C | 1 | a0001c0001t0001g0186 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.92-4622_92-4576del others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431230 | |||||
| chr11:1431230
|
CCAGCAGT others(87): Show |
C | 1 | a0001c0001t0024g0299 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.92-4669_92-4576del others(94): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431230 | |||||
| chr11:1431252
|
GTCTGGTC others(226): Show |
G | 1 | a0002c0002t0002g0158 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.92-4787_92-4555del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431252 | ||||||
| chr11:1431265
|
T | C | 1 | a0002c0002t0007g0345 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.92-4775T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431265 | ||||||
| chr11:1431277
|
T | C | 121 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0063others(118): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.92-4763T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431277 | ||||||
| chr11:1431277
|
TCAGCAGT others(1080): Show |
T | 5 | a0001c0001t0003g0265a0001c0001t0003g0271a0001c0001t0061g0266others(2): Show | 5 | NA18944.hp2 NA18953.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-4340_92-3254del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431277 | |||||
| chr11:1431297
|
C | CGG | 4 | a0001c0001t0001g0009a0001c0001t0001g0192a0001c0001t0043g0050others(1): Show | 4 | HG02486.hp2 HG02647.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-4742_92-4741dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431297 | |||||
| chr11:1431297
|
C | CGGTCTGG others(89): Show |
1 | a0002c0002t0008g0071 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.92-4742_92-4647dup others(96): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431297 | |||||
| chr11:1431297
|
CGGTCTGG others(939): Show |
C | 1 | a0001c0001t0001g0072 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.92-4716_92-3771del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431297 | |||||
| chr11:1431299
|
GTCTGGTC others(85): Show |
G | 1 | a0002c0002t0008g0181 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.92-4740_92-4649del others(92): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431299 | ||||||
| chr11:1431324
|
T | C | 83 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(80): Show | 84 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.92-4716T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431324 | ||||||
| chr11:1431324
|
T | TCAGCAGT others(138): Show |
1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92-4694_92-4693ins others(145): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431324 | |||||
| chr11:1431346
|
GTCTGGTC others(510): Show |
G | 1 | a0002c0002t0053g0139 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.92-4693_92-4177del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431346 | ||||||
| chr11:1431371
|
T | C | 86 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0023others(83): Show | 88 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.92-4669T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431371 | ||||||
| chr11:1431393
|
GTCTGGTC others(132): Show |
G | 5 | a0002c0002t0002g0098a0002c0002t0002g0164a0002c0002t0002g0166others(2): Show | 5 | HG00544.hp2 HG02040.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-4646_92-4508del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431393 | ||||||
| chr11:1431393
|
GTCTGGTC others(273): Show |
G | 1 | a0001c0001t0006g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.92-4646_92-4367del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431393 | ||||||
| chr11:1431399
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92-4641T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431399 | ||||||
| chr11:1431418
|
T | C | 101 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(98): Show | 105 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.92-4622T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431418 | ||||||
| chr11:1431418
|
TCAGCAGT others(40): Show |
T | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.92-4387_92-4341del others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431418 | |||||
| chr11:1431418
|
TCAGCAGT others(1127): Show |
T | 2 | a0001c0001t0065g0256a0002c0002t0005g0276 | 2 | HG01175.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.92-4340_92-3207del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431418 | |||||
| chr11:1431430
|
GTCTTCTG others(1644): Show |
G | 1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.92-4575_92-2925del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431430 | |||||
| chr11:1431432
|
C | T | 2 | a0001c0001t0006g0215a0001c0001t0074g0213 | 2 | HG01261.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.92-4608C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431432 | ||||||
| chr11:1431438
|
C | CGG | 5 | a0002c0002t0002g0075a0002c0002t0002g0086a0002c0002t0005g0005others(2): Show | 6 | HG00438.hp1 HG00673.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-4601_92-4600dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431438 | |||||
| chr11:1431440
|
GTCTGGTC others(179): Show |
G | 2 | a0001c0001t0011g0310a0002c0002t0008g0167 | 2 | HG00140.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.92-4599_92-4414del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431440 | ||||||
| chr11:1431440
|
GTCTGGTC others(273): Show |
G | 4 | a0002c0002t0007g0306a0002c0002t0020g0125a0002c0002t0040g0298others(1): Show | 4 | HG01255.hp1 HG03704.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-4599_92-4320del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431440 | ||||||
| chr11:1431440
|
GTCTGGTC others(416): Show |
G | 1 | a0002c0002t0002g0103 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.92-4599_92-4177del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431440 | ||||||
| chr11:1431448
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.92-4592A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431448 | ||||||
| chr11:1431465
|
C | T | 19 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0107others(16): Show | 19 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.92-4575C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431465 | ||||||
| chr11:1431471
|
G | T | 1 | a0001c0003t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.92-4569G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431471 | ||||||
| chr11:1431474
|
A | G | 1 | a0002c0002t0007g0345 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.92-4566A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431474 | ||||||
| chr11:1431476
|
C | T | 1 | a0001c0001t0025g0143 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.92-4564C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431476 | ||||||
| chr11:1431479
|
C | T | 1 | a0001c0016t0018g0183 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.92-4561C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431479 | ||||||
| chr11:1431485
|
C | CGG | 8 | a0001c0001t0001g0087a0001c0001t0001g0107a0001c0001t0009g0153others(5): Show | 8 | HG00280.hp1 HG00408.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-4554_92-4553dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431485 | |||||
| chr11:1431487
|
GTCTGGTC others(38): Show |
G | 1 | a0002c0002t0019g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.92-4552_92-4508del others(45): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431487 | ||||||
| chr11:1431487
|
GTCTGGTC others(132): Show |
G | 1 | a0001c0001t0043g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.92-4552_92-4414del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431487 | ||||||
| chr11:1431512
|
C | T | 20 | a0001c0001t0001g0048a0001c0001t0001g0087a0001c0001t0001g0107others(17): Show | 20 | HG00280.hp1 HG00408.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.92-4528C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431512 | ||||||
| chr11:1431512
|
CCAGCAGT others(986): Show |
C | 3 | a0001c0001t0004g0175a0001c0001t0004g0180a0001c0016t0018g0183 | 3 | HG01993.hp2 HG02273.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.92-4340_92-3348del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431512 | |||||
| chr11:1431532
|
C | CGG | 4 | a0002c0002t0002g0169a0002c0002t0002g0170a0002c0002t0010g0233others(1): Show | 4 | HG01099.hp2 HG01515.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-4507_92-4506dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431532 | |||||
| chr11:1431532
|
CGGTCTGG others(704): Show |
C | 4 | a0002c0002t0002g0075a0002c0002t0002g0086a0002c0002t0005g0005others(1): Show | 5 | HG00438.hp1 NA18995.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-4270_92-3560del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431532 | |||||
| chr11:1431559
|
C | T | 18 | a0001c0001t0001g0087a0001c0001t0001g0107a0001c0001t0003g0200others(15): Show | 18 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.92-4481C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431559 | ||||||
| chr11:1431579
|
C | CGGGGTCT others(138): Show |
2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.92-4459_92-4458ins others(145): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431579 | |||||
| chr11:1431606
|
C | T | 18 | a0001c0001t0001g0087a0001c0001t0001g0107a0001c0001t0006g0197others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.92-4434C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431606 | ||||||
| chr11:1431626
|
C | CGG | 8 | a0001c0001t0001g0087a0001c0001t0001g0107a0002c0002t0002g0159others(5): Show | 8 | HG00280.hp1 HG00738.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-4413_92-4412dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431626 | |||||
| chr11:1431626
|
C | T | 1 | a0002c0002t0023g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.92-4414C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431626 | ||||||
| chr11:1431653
|
C | CCAGCAGT others(40): Show |
6 | a0001c0001t0001g0049a0001c0001t0003g0228a0001c0001t0031g0012others(3): Show | 7 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-4317_92-4271dup others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431653 | |||||
| chr11:1431653
|
C | T | 62 | a0001c0001t0001g0087a0001c0001t0001g0107a0001c0001t0001g0313others(59): Show | 64 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.92-4387C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431653 | ||||||
| chr11:1431673
|
C | A | 1 | a0001c0001t0013g0022 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.92-4367C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431673 | ||||||
| chr11:1431673
|
C | CGG | 4 | a0001c0001t0006g0197a0001c0001t0006g0226a0002c0002t0010g0233others(1): Show | 4 | HG00735.hp1 HG02165.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-4366_92-4365dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431673 | |||||
| chr11:1431673
|
C | CGGTCTGG others(749): Show |
1 | a0002c0002t0023g0254 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.92-4341_92-4340ins others(756): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431673 | |||||
| chr11:1431673
|
CGGTCTGG others(89): Show |
C | 2 | a0002c0002t0019g0042a0002c0002t0019g0043 | 2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.92-4270_92-4175del others(96): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431673 | |||||
| chr11:1431673
|
CGGTCTGG others(563): Show |
C | 1 | a0001c0001t0057g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.92-4340_92-3771del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431673 | |||||
| chr11:1431675
|
GTCTGGTC others(181): Show |
G | 1 | a0002c0002t0002g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92-4364_92-4177del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431675 | ||||||
| chr11:1431700
|
T | C | 67 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0023others(64): Show | 68 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.92-4340T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431700 | ||||||
| chr11:1431720
|
C | CGG | 9 | a0001c0001t0006g0225a0001c0001t0018g0334a0001c0001t0067g0252others(6): Show | 10 | HG00621.hp2 HG00738.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-4319_92-4318dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431720 | |||||
| chr11:1431720
|
C | CGGTCTGG others(702): Show |
1 | a0001c0001t0021g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.92-4294_92-4293ins others(709): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431720 | |||||
| chr11:1431720
|
C | CGGTCTGG others(749): Show |
1 | a0001c0001t0003g0288 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.92-4294_92-4293ins others(756): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431720 | |||||
| chr11:1431720
|
CGGTCTGG others(42): Show |
C | 2 | a0002c0002t0002g0158a0002c0002t0015g0330 | 2 | HG02155.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.92-4270_92-4222del others(49): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431720 | |||||
| chr11:1431720
|
CGGTCTGG others(185): Show |
C | 2 | a0001c0001t0018g0137a0002c0008t0005g0278 | 2 | HG01261.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.92-4293_92-4102del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431720 | |||||
| chr11:1431720
|
CGGTCTGG others(516): Show |
C | 5 | a0001c0001t0001g0046a0002c0002t0019g0021a0002c0005t0034g0055others(2): Show | 5 | HG01346.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-4293_92-3771del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431720 | |||||
| chr11:1431747
|
T | C | 57 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(54): Show | 58 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.92-4293T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431747 | ||||||
| chr11:1431747
|
TCAGCAGT others(610): Show |
T | 1 | a0002c0002t0008g0181 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.92-4270_92-3654del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431747 | |||||
| chr11:1431767
|
CGG | C | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(90): Show | 96 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.92-4270_92-4269del others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431767 | |||||
| chr11:1431767
|
CGGGGTCT others(138): Show |
C | 1 | a0002c0002t0005g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.92-4270_92-4126del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431767 | |||||
| chr11:1431769
|
G | GTCTGGTC others(180): Show |
1 | a0002c0002t0008g0078 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.92-4271_92-4270ins others(187): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431769 | ||||||
| chr11:1431769
|
G | GTCTGGTC others(38): Show |
1 | a0001c0006t0027g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.92-4271_92-4270ins others(45): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431769 | ||||||
| chr11:1431769
|
G | GTCTGGTC others(230): Show |
1 | a0002c0002t0015g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.92-4271_92-4270ins others(237): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431769 | ||||||
| chr11:1431769
|
G | GTCTGGTC others(273): Show |
1 | a0002c0002t0049g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.92-4271_92-4270ins others(280): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431769 | ||||||
| chr11:1431769
|
G | GTCTGGTC others(85): Show |
3 | a0001c0001t0021g0206a0001c0001t0021g0221a0001c0001t0036g0300 | 3 | HG00323.hp2 HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.92-4271_92-4270ins others(92): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431769 | ||||||
| chr11:1431769
|
G | GTCTGGTC others(132): Show |
1 | a0001c0001t0001g0053 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.92-4271_92-4270ins others(139): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431769 | ||||||
| chr11:1431769
|
G | GTCTGGTC others(179): Show |
1 | a0001c0001t0001g0052 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.92-4271_92-4270ins others(186): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431769 | ||||||
| chr11:1431769
|
G | GTCTGGTC others(226): Show |
1 | a0001c0001t0004g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.92-4271_92-4270ins others(233): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431769 | ||||||
| chr11:1431769
|
G | GTCTGGTC others(273): Show |
1 | a0002c0002t0023g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.92-4271_92-4270ins others(280): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431769 | ||||||
| chr11:1431769
|
G | GTCTGGTC others(418): Show |
1 | a0001c0001t0001g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.92-4271_92-4270ins others(425): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431769 | ||||||
| chr11:1431769
|
G | GTCTGGTC others(2171): Show |
1 | a0002c0002t0016g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.92-4271_92-4270ins others(2178): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431769 | ||||||
| chr11:1431769
|
G | GTCTGGTC others(2502): Show |
1 | a0002c0002t0010g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.92-4271_92-4270ins others(2509): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431769 | ||||||
| chr11:1431769
|
GGGTCTGG others(40): Show |
G | 1 | a0001c0001t0001g0048 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.92-4174_92-4128del others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431769 | |||||
| chr11:1431796
|
T | C | 49 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(46): Show | 50 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.92-4244T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431796 | ||||||
| chr11:1431816
|
C | CGG | 7 | a0001c0001t0001g0010a0001c0001t0006g0197a0001c0001t0006g0214others(4): Show | 7 | HG00323.hp1 HG00735.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-4223_92-4222dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431816 | |||||
| chr11:1431816
|
CGGTCTGG others(89): Show |
C | 1 | a0002c0002t0002g0159 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.92-4197_92-4102del others(96): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431816 | |||||
| chr11:1431818
|
GTCTGGTC others(465): Show |
G | 1 | a0002c0002t0002g0132 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.92-4221_92-3750del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431818 | ||||||
| chr11:1431818
|
GTCTGGTC others(1264): Show |
G | 1 | a0001c0003t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.92-4221_92-2951del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431818 | ||||||
| chr11:1431818
|
GTCTGGTC others(1311): Show |
G | 1 | a0001c0003t0001g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.92-4221_92-2904del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431818 | ||||||
| chr11:1431843
|
T | C | 53 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.92-4197T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431843 | ||||||
| chr11:1431843
|
TCAGCAGT others(89): Show |
T | 1 | a0002c0002t0002g0170 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.92-4150_92-4055del others(96): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431843 | |||||
| chr11:1431863
|
C | CGG | 13 | a0001c0001t0003g0288a0001c0001t0018g0334a0001c0001t0021g0242others(10): Show | 14 | HG00621.hp2 HG00738.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.92-4176_92-4175dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431863 | |||||
| chr11:1431863
|
CGGTCTGG others(42): Show |
C | 2 | a0001c0001t0011g0310a0002c0002t0008g0167 | 2 | HG00140.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.92-4150_92-4102del others(49): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431863 | |||||
| chr11:1431865
|
GTCTGGTC others(87): Show |
G | 3 | a0001c0001t0009g0153a0002c0002t0008g0151a0005c0010t0002g0085 | 3 | HG00408.hp2 NA18612.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.92-4174_92-4081del others(94): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431865 | ||||||
| chr11:1431865
|
GTCTGGTC others(418): Show |
G | 17 | a0001c0001t0001g0313a0002c0002t0002g0149a0002c0002t0007g0294others(14): Show | 18 | HG01952.hp2 HG01975.hp2 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.92-4174_92-3750del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431865 | ||||||
| chr11:1431865
|
GTCTGGTC others(465): Show |
G | 1 | a0002c0002t0017g0301 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.92-4174_92-3703del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431865 | ||||||
| chr11:1431865
|
GTCTGGTC others(1264): Show |
G | 2 | a0001c0001t0006g0215a0001c0001t0074g0213 | 2 | HG01261.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.92-4174_92-2904del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431865 | ||||||
| chr11:1431890
|
T | C | 59 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(56): Show | 60 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.92-4150T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431890 | ||||||
| chr11:1431890
|
T | TCAGCAGT others(40): Show |
1 | a0001c0001t0003g0201 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.92-4128_92-4127ins others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431890 | |||||
| chr11:1431890
|
T | TCAGCAGT others(89): Show |
1 | a0001c0001t0003g0200 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.92-4128_92-4127ins others(96): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431890 | |||||
| chr11:1431910
|
CGG | C | 53 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(50): Show | 55 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.92-4127_92-4126del others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431910 | |||||
| chr11:1431912
|
G | GTCTGGTC others(38): Show |
3 | a0001c0001t0001g0011a0001c0001t0003g0220a0001c0001t0059g0041 | 3 | HG01516.hp2 HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.92-4128_92-4127ins others(45): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431912 | ||||||
| chr11:1431912
|
G | GTCTGGTC others(85): Show |
1 | a0002c0002t0005g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.92-4128_92-4127ins others(92): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431912 | ||||||
| chr11:1431912
|
G | GTCTGGTC others(988): Show |
1 | a0001c0001t0044g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.92-4128_92-4127ins others(995): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431912 | ||||||
| chr11:1431912
|
G | GTCTGGTC others(183): Show |
1 | a0002c0002t0008g0116 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.92-4128_92-4127ins others(190): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431912 | ||||||
| chr11:1431912
|
G | GTCTGGTC others(39): Show |
1 | a0001c0001t0003g0219 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.92-4128_92-4127ins others(46): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431912 | ||||||
| chr11:1431912
|
GGGTCTGG others(40): Show |
G | 5 | a0002c0002t0002g0098a0002c0002t0002g0164a0002c0002t0002g0166others(2): Show | 5 | HG00544.hp2 HG02040.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-4007_92-3961del others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431912 | |||||
| chr11:1431912
|
GGGTCTGG others(1217): Show |
G | 3 | a0001c0001t0004g0161a0001c0001t0004g0179a0001c0001t0004g0185 | 3 | HG00639.hp2 HG01069.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.92-4103_92-2880del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431912 | |||||
| chr11:1431939
|
C | T | 42 | a0001c0001t0001g0063a0001c0001t0001g0099a0001c0001t0001g0123others(39): Show | 43 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.92-4101C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431939 | ||||||
| chr11:1431951
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92-4089G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431951 | ||||||
| chr11:1431951
|
GTCTTCTG others(370): Show |
G | 1 | a0002c0002t0007g0345 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.92-4088_92-3712del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431951 | ||||||
| chr11:1431959
|
C | CGG | 8 | a0001c0001t0001g0087a0001c0001t0001g0107a0001c0001t0003g0201others(5): Show | 8 | HG00280.hp1 HG01099.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-4080_92-4079dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431959 | |||||
| chr11:1431959
|
C | CGGGGTCT others(2132): Show |
1 | a0001c0001t0001g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.92-4079_92-4078ins others(2139): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431959 | |||||
| chr11:1431986
|
C | T | 10 | a0001c0001t0001g0192a0001c0001t0003g0267a0001c0001t0003g0272others(7): Show | 10 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-4054C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1431986 | ||||||
| chr11:1431986
|
CCAGCAGT others(1123): Show |
C | 1 | a0001c0001t0043g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.92-4009_92-2880del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1431986 | |||||
| chr11:1432006
|
C | CGG | 10 | a0001c0001t0001g0023a0001c0001t0001g0087a0001c0001t0001g0107others(7): Show | 10 | HG00280.hp1 HG00673.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-4033_92-4032dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432006 | |||||
| chr11:1432006
|
C | CGGGGTCT others(1795): Show |
1 | a0002c0002t0023g0254 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.92-4032_92-4031ins others(1802): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432006 | |||||
| chr11:1432006
|
C | CGGTCTGG others(2034): Show |
1 | a0002c0002t0008g0116 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.92-3961_92-3960ins others(2041): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432006 | |||||
| chr11:1432008
|
GTCTGGTC others(38): Show |
G | 1 | a0001c0001t0001g0048 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.92-4031_92-3987del others(45): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432008 | ||||||
| chr11:1432033
|
C | CCAGCAGT others(134): Show |
1 | a0001c0001t0036g0300 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.92-3961_92-3960ins others(141): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432033 | |||||
| chr11:1432033
|
C | T | 36 | a0001c0001t0001g0049a0001c0001t0003g0239a0001c0001t0003g0288others(33): Show | 37 | HG00323.hp1 HG00609.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.92-4007C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432033 | ||||||
| chr11:1432033
|
CCAGCAGT others(40): Show |
C | 1 | a0001c0001t0011g0310 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.92-3843_92-3797del others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432033 | |||||
| chr11:1432053
|
C | CGG | 9 | a0001c0001t0001g0192a0001c0001t0013g0311a0002c0002t0002g0015others(6): Show | 10 | HG00673.hp2 HG00738.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-3986_92-3985dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432053 | |||||
| chr11:1432053
|
C | CGGTCTGG others(91): Show |
1 | a0002c0002t0005g0224 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.92-3961_92-3960ins others(98): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432053 | |||||
| chr11:1432053
|
CGGTCTGG others(183): Show |
C | 1 | a0002c0002t0002g0169 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.92-3960_92-3771del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432053 | |||||
| chr11:1432054
|
G | A | 1 | a0002c0002t0051g0077 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.92-3986G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432054 | ||||||
| chr11:1432060
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-3980G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432060 | ||||||
| chr11:1432080
|
T | C | 64 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 65 | HG00280.hp1 HG00673.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.92-3960T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432080 | ||||||
| chr11:1432080
|
T | TCAGCAGT others(2177): Show |
1 | a0001c0001t0004g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.92-3914_92-3913ins others(2184): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432080 | |||||
| chr11:1432080
|
T | TCAGCAGT others(2224): Show |
1 | a0002c0002t0023g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.92-3914_92-3913ins others(2231): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432080 | |||||
| chr11:1432080
|
T | TCAGCAGT others(1846): Show |
1 | a0002c0002t0049g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.92-3914_92-3913ins others(1853): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432080 | |||||
| chr11:1432080
|
TCAGCAGT others(277): Show |
T | 1 | a0002c0002t0002g0098 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.92-3796_92-3513del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432080 | |||||
| chr11:1432100
|
C | CGG | 6 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0034others(3): Show | 6 | HG00673.hp2 HG01361.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-3939_92-3938dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432100 | |||||
| chr11:1432100
|
C | CGGTCTGG others(422): Show |
1 | a0002c0002t0023g0223 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.92-3914_92-3913ins others(429): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432100 | |||||
| chr11:1432127
|
T | C | 68 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(65): Show | 69 | HG00280.hp1 HG00323.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.92-3913T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432127 | ||||||
| chr11:1432127
|
TCAGCAGT others(230): Show |
T | 1 | a0002c0002t0020g0148 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.92-3796_92-3560del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432127 | |||||
| chr11:1432134
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-3906T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432134 | ||||||
| chr11:1432147
|
C | CGG | 5 | a0001c0001t0001g0127a0001c0001t0006g0225a0001c0001t0013g0311others(2): Show | 5 | HG01109.hp1 HG01361.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-3892_92-3891dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432147 | |||||
| chr11:1432147
|
CGGTCTGG others(89): Show |
C | 2 | a0002c0002t0002g0170a0002c0002t0015g0330 | 2 | HG01099.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.92-3866_92-3771del others(96): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432147 | |||||
| chr11:1432174
|
T | C | 64 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.92-3866T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432174 | ||||||
| chr11:1432181
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-3859T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432181 | ||||||
| chr11:1432194
|
C | CGG | 10 | a0001c0001t0001g0030a0001c0001t0001g0141a0001c0001t0003g0241others(7): Show | 12 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.92-3845_92-3844dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432194 | |||||
| chr11:1432194
|
C | CGGTCTGG others(281): Show |
3 | a0001c0001t0021g0206a0001c0001t0021g0221a0002c0002t0002g0176 | 3 | HG00741.hp1 HG01081.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.92-3797_92-3796ins others(288): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432194 | |||||
| chr11:1432194
|
CGGTCTGG others(42): Show |
C | 2 | a0001c0001t0001g0186a0002c0002t0019g0043 | 2 | HG03225.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.92-3819_92-3771del others(49): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432194 | |||||
| chr11:1432221
|
T | C | 84 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(81): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.92-3819T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432221 | ||||||
| chr11:1432221
|
T | TCAGCAGT others(89): Show |
1 | a0002c0002t0005g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.92-3797_92-3796ins others(96): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432221 | |||||
| chr11:1432221
|
TCAGCAGT others(42): Show |
T | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.92-3796_92-3748del others(49): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432221 | |||||
| chr11:1432221
|
TCAGCAGT others(136): Show |
T | 4 | a0002c0002t0002g0164a0002c0002t0002g0166a0002c0002t0020g0156others(1): Show | 4 | HG00544.hp2 HG02040.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-3796_92-3654del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432221 | |||||
| chr11:1432221
|
TCAGCAGT others(324): Show |
T | 1 | a0002c0002t0002g0158 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.92-3796_92-3466del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432221 | |||||
| chr11:1432241
|
CGG | C | 66 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(63): Show | 66 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.92-3796_92-3795del others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432241 | |||||
| chr11:1432243
|
G | GGGTCTGG others(40): Show |
1 | a0001c0001t0006g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.92-3676_92-3630dup others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432243 | |||||
| chr11:1432243
|
G | GGGTCTGG others(230): Show |
8 | a0001c0001t0003g0239a0001c0001t0032g0195a0001c0001t0032g0209others(5): Show | 8 | HG00609.hp2 HG00639.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-3748_92-3747ins others(237): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432243 | |||||
| chr11:1432243
|
G | GGGTCTGG others(277): Show |
4 | a0001c0001t0001g0049a0001c0001t0004g0051a0001c0001t0027g0129others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-3748_92-3747ins others(284): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432243 | |||||
| chr11:1432243
|
G | GGGTCTGG others(324): Show |
1 | a0001c0001t0031g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.92-3748_92-3747ins others(331): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432243 | |||||
| chr11:1432243
|
G | GGGTCTGG others(87): Show |
1 | a0001c0001t0006g0226 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.92-3723_92-3630dup others(94): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432243 | |||||
| chr11:1432243
|
G | GGGTCTGG others(134): Show |
1 | a0002c0002t0005g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.92-3770_92-3630dup others(141): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432243 | |||||
| chr11:1432243
|
G | GGGTCTGG others(181): Show |
1 | a0002c0002t0010g0004 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.92-3630_92-3629ins others(188): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432243 | |||||
| chr11:1432243
|
G | GGGTCTGG others(2410): Show |
1 | a0001c0001t0001g0127 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.92-3724_92-3723ins others(2417): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432243 | |||||
| chr11:1432243
|
G | GGGTCTGG others(1552): Show |
1 | a0001c0001t0036g0300 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.92-3771_92-3770ins others(1559): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432243 | |||||
| chr11:1432243
|
G | GTCTGGTC others(38): Show |
1 | a0001c0001t0001g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.92-3797_92-3796ins others(45): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432243 | ||||||
| chr11:1432243
|
G | GTCTGGTC others(324): Show |
1 | a0001c0001t0044g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.92-3797_92-3796ins others(331): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432243 | ||||||
| chr11:1432243
|
G | GTCTGGTC others(133): Show |
1 | a0001c0001t0024g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-3797_92-3796ins others(140): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432243 | ||||||
| chr11:1432243
|
G | GTCTGGTC others(226): Show |
1 | a0001c0001t0001g0052 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.92-3797_92-3796ins others(233): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432243 | ||||||
| chr11:1432243
|
G | GTCTGGTC others(273): Show |
1 | a0001c0001t0001g0053 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.92-3797_92-3796ins others(280): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432243 | ||||||
| chr11:1432245
|
G | T | 1 | a0002c0007t0010g0244 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.92-3795G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432245 | ||||||
| chr11:1432246
|
T | C | 1 | a0002c0007t0010g0244 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.92-3794T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432246 | ||||||
| chr11:1432270
|
C | T | 34 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0099others(31): Show | 34 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.92-3770C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432270 | ||||||
| chr11:1432290
|
C | CGG | 27 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0099others(24): Show | 27 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.92-3749_92-3748dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432290 | |||||
| chr11:1432292
|
GTCTGGTC others(461): Show |
G | 2 | a0001c0001t0003g0267a0001c0001t0003g0272 | 2 | HG00423.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.92-3747_92-3280del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432292 | ||||||
| chr11:1432317
|
C | T | 8 | a0001c0001t0001g0048a0001c0001t0003g0200a0001c0001t0003g0201others(5): Show | 8 | HG00408.hp2 HG00438.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-3723C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432317 | ||||||
| chr11:1432339
|
GTCTGGTC others(179): Show |
G | 1 | a0002c0008t0005g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.92-3700_92-3515del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432339 | ||||||
| chr11:1432339
|
GTCTGGTC others(226): Show |
G | 1 | a0002c0002t0019g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.92-3700_92-3468del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432339 | ||||||
| chr11:1432339
|
GTCTGGTC others(273): Show |
G | 3 | a0001c0001t0009g0153a0002c0002t0008g0151a0005c0010t0002g0085 | 3 | HG00408.hp2 NA18612.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.92-3700_92-3421del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432339 | ||||||
| chr11:1432364
|
C | T | 51 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0059others(48): Show | 53 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.92-3676C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432364 | ||||||
| chr11:1432364
|
CCAGCAGT others(87): Show |
C | 2 | a0001c0003t0004g0290a0002c0002t0058g0325 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.92-3582_92-3489del others(94): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432364 | |||||
| chr11:1432384
|
C | CGGTCTGG others(231): Show |
1 | a0001c0001t0070g0210 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.92-3630_92-3629ins others(238): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432384 | |||||
| chr11:1432385
|
G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0130a0001c0001t0003g0268 | 3 | HG00621.hp1 HG01496.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.92-3655G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432385 | ||||||
| chr11:1432386
|
GTCTGGTC others(508): Show |
G | 2 | a0001c0001t0001g0048a0002c0002t0002g0015 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.92-3653_92-3139del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432386 | ||||||
| chr11:1432411
|
T | C | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(90): Show | 94 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.92-3629T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432411 | ||||||
| chr11:1432432
|
G | A | 38 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0061others(35): Show | 38 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.92-3608G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432432 | ||||||
| chr11:1432458
|
T | C | 96 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(93): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.92-3582T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432458 | ||||||
| chr11:1432470
|
G | C | 2 | a0002c0002t0002g0169a0002c0002t0002g0170 | 2 | HG01099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.92-3570G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432470 | ||||||
| chr11:1432479
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0097 | 2 | NA19005.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.92-3561G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432479 | ||||||
| chr11:1432498
|
A | G | 1 | a0004c0009t0008g0178 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.92-3542A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432498 | ||||||
| chr11:1432505
|
T | C | 107 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(104): Show | 108 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.92-3535T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432505 | ||||||
| chr11:1432505
|
T | TCAGCAGT others(935): Show |
1 | a0002c0002t0002g0176 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.92-3466_92-3465ins others(942): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432505 | |||||
| chr11:1432505
|
T | TCAGCAGT others(1407): Show |
1 | a0001c0001t0021g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.92-3466_92-3465ins others(1414): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432505 | |||||
| chr11:1432505
|
T | TCAGCAGT others(1407): Show |
1 | a0001c0001t0021g0221 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.92-3466_92-3465ins others(1414): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432505 | |||||
| chr11:1432505
|
T | TCAGCAGT others(87): Show |
1 | a0001c0001t0003g0201 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.92-3253_92-3160dup others(94): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432505 | |||||
| chr11:1432505
|
T | TCAGCAGT others(185): Show |
1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92-3489_92-3488ins others(192): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432505 | |||||
| chr11:1432505
|
TCAGCAGT others(40): Show |
T | 1 | a0002c0002t0053g0139 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.92-3206_92-3160del others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432505 | |||||
| chr11:1432505
|
TCAGCAGT others(134): Show |
T | 4 | a0002c0002t0002g0164a0002c0002t0002g0166a0002c0002t0020g0156others(1): Show | 4 | HG00544.hp2 HG02040.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-3300_92-3160del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432505 | |||||
| chr11:1432517
|
G | C | 2 | a0002c0002t0002g0169a0002c0002t0002g0170 | 2 | HG01099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.92-3523G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432517 | ||||||
| chr11:1432519
|
C | T | 2 | a0001c0001t0004g0190a0001c0001t0057g0184 | 2 | HG02738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.92-3521C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432519 | ||||||
| chr11:1432545
|
A | G | 1 | a0004c0009t0008g0178 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.92-3495A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432545 | ||||||
| chr11:1432552
|
C | T | 99 | a0001c0001t0001g0049a0001c0001t0001g0063a0001c0001t0001g0069others(96): Show | 103 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.92-3488C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432552 | ||||||
| chr11:1432592
|
A | G | 1 | a0004c0009t0008g0178 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.92-3448A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432592 | ||||||
| chr11:1432599
|
C | G | 1 | a0001c0001t0009g0187 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.92-3441C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432599 | ||||||
| chr11:1432599
|
C | T | 65 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0099others(62): Show | 66 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.92-3441C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432599 | ||||||
| chr11:1432619
|
C | CGGTCTGG others(1554): Show |
1 | a0001c0001t0014g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.92-3395_92-3394ins others(1561): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432619 | |||||
| chr11:1432620
|
G | C | 1 | a0002c0002t0041g0144 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.92-3420G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432620 | ||||||
| chr11:1432646
|
C | T | 43 | a0001c0001t0001g0010a0001c0001t0001g0192a0001c0001t0009g0153others(40): Show | 44 | HG00408.hp2 HG00621.hp2 HG01346.hp1 others(41): Show |
intron_variant | MODIFIER | c.92-3394C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432646 | ||||||
| chr11:1432666
|
C | G | 2 | a0002c0002t0033g0286a0002c0002t0066g0285 | 2 | HG02738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.92-3374C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432666 | ||||||
| chr11:1432693
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0004g0080others(6): Show | 10 | HG01261.hp2 HG02027.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-3347C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432693 | ||||||
| chr11:1432740
|
C | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0003g0236others(7): Show | 11 | HG01109.hp1 HG01261.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-3300C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432740 | ||||||
| chr11:1432745
|
A | G | 1 | a0001c0001t0018g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.92-3295A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432745 | ||||||
| chr11:1432770
|
A | AGGTTTTG others(322): Show |
1 | a0001c0001t0001g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.92-3249_92-3248ins others(329): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432770 | |||||
| chr11:1432770
|
A | G | 2 | a0001c0001t0018g0137a0002c0008t0005g0278 | 2 | HG01261.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.92-3270A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432770 | ||||||
| chr11:1432787
|
C | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0186a0001c0001t0001g0192others(8): Show | 12 | HG01109.hp1 HG01261.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.92-3253C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432787 | ||||||
| chr11:1432792
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0018g0137 | 2 | HG01261.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.92-3248A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432792 | ||||||
| chr11:1432799
|
GTCTTCTG others(275): Show |
G | 2 | a0002c0002t0002g0169a0002c0002t0002g0170 | 2 | HG01099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.92-3206_92-2925del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432799 | |||||
| chr11:1432817
|
A | G | 3 | a0001c0001t0018g0137a0002c0002t0019g0042a0002c0008t0005g0278 | 3 | HG01261.hp2 HG01884.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.92-3223A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432817 | ||||||
| chr11:1432834
|
C | T | 21 | a0001c0001t0001g0009a0001c0001t0001g0046a0001c0001t0001g0186others(18): Show | 22 | HG01109.hp1 HG01255.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.92-3206C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432834 | ||||||
| chr11:1432834
|
CCAGCAGT others(40): Show |
C | 6 | a0001c0001t0001g0072a0001c0001t0003g0222a0001c0001t0003g0265others(3): Show | 6 | HG00438.hp1 HG01496.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-3006_92-2960del others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432834 | |||||
| chr11:1432839
|
A | G | 2 | a0001c0001t0018g0137a0002c0002t0019g0042 | 2 | HG01261.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.92-3201A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432839 | ||||||
| chr11:1432864
|
A | G | 5 | a0001c0001t0018g0137a0001c0006t0027g0142a0002c0002t0015g0330others(2): Show | 5 | HG01261.hp2 HG02258.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-3176A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432864 | ||||||
| chr11:1432881
|
T | C | 152 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0023others(149): Show | 155 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.92-3159T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432881 | ||||||
| chr11:1432886
|
A | G | 6 | a0001c0001t0018g0137a0001c0006t0027g0142a0002c0002t0015g0330others(3): Show | 6 | HG01261.hp2 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-3154A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432886 | ||||||
| chr11:1432893
|
GTCTTCTG others(181): Show |
G | 20 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0073others(17): Show | 20 | HG00280.hp2 HG00438.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.92-3067_92-2880del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432893 | |||||
| chr11:1432911
|
A | G | 12 | a0001c0001t0001g0186a0001c0001t0018g0137a0001c0001t0076g0182others(9): Show | 13 | HG01109.hp1 HG01261.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-3129A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432911 | ||||||
| chr11:1432928
|
T | C | 121 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 122 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.92-3112T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432928 | ||||||
| chr11:1432933
|
A | AGTGAGCG others(40): Show |
1 | a0001c0006t0001g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.92-3083_92-3082ins others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432933 | |||||
| chr11:1432933
|
A | G | 11 | a0001c0001t0001g0186a0001c0001t0018g0137a0001c0001t0076g0182others(8): Show | 12 | HG01109.hp1 HG01261.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.92-3107A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432933 | ||||||
| chr11:1432940
|
GTCTTCTG others(134): Show |
G | 2 | a0001c0001t0001g0089a0001c0001t0011g0295 | 2 | NA18952.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.92-3020_92-2880del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432940 | |||||
| chr11:1432950
|
GTCTGGTC others(179): Show |
G | 8 | a0001c0001t0001g0191a0001c0001t0004g0175a0001c0001t0004g0180others(5): Show | 8 | HG01255.hp2 HG01891.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-3089_92-2904del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432950 | ||||||
| chr11:1432958
|
A | G | 15 | a0001c0001t0001g0009a0001c0001t0001g0186a0001c0001t0018g0137others(12): Show | 16 | HG01109.hp1 HG01261.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.92-3082A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432958 | ||||||
| chr11:1432975
|
T | C | 106 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0030others(103): Show | 108 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.92-3065T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432975 | ||||||
| chr11:1432975
|
T | TCAGCGGT others(40): Show |
1 | a0001c0001t0078g0205 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.92-3061_92-3060ins others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432975 | |||||
| chr11:1432980
|
A | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0186a0001c0001t0018g0137others(13): Show | 17 | HG01109.hp1 HG01261.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.92-3060A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432980 | ||||||
| chr11:1432987
|
GTCTTCTG others(87): Show |
G | 7 | a0001c0001t0001g0069a0001c0001t0009g0187a0002c0002t0015g0330others(4): Show | 8 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-2973_92-2880del others(94): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432987 | |||||
| chr11:1432995
|
C | CGG | 3 | a0002c0002t0002g0075a0002c0002t0005g0005a0002c0002t0023g0223 | 4 | HG01167.hp2 NA18995.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-3044_92-3043dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1432995 | |||||
| chr11:1432997
|
GTCTGGTC others(132): Show |
G | 3 | a0001c0001t0001g0189a0001c0001t0004g0177a0001c0001t0057g0184 | 3 | HG01123.hp2 HG01192.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.92-3042_92-2904del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1432997 | ||||||
| chr11:1433005
|
A | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0186a0001c0001t0018g0137others(9): Show | 13 | HG01109.hp1 HG01261.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-3035A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433005 | ||||||
| chr11:1433022
|
T | C | 81 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0057others(78): Show | 82 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.92-3018T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433022 | ||||||
| chr11:1433022
|
T | TCAGCAGT others(1975): Show |
1 | a0001c0001t0045g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.92-2960_92-2959ins others(1982): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433022 | |||||
| chr11:1433027
|
A | G | 14 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0186others(11): Show | 15 | HG01109.hp1 HG01261.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.92-3013A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433027 | ||||||
| chr11:1433034
|
G | C | 1 | a0002c0002t0053g0139 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.92-3006G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433034 | ||||||
| chr11:1433034
|
GTCTTCTG others(40): Show |
G | 9 | a0001c0001t0001g0063a0001c0001t0001g0099a0002c0002t0002g0103others(6): Show | 9 | HG01255.hp1 HG02132.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-2959_92-2913del others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433034 | |||||
| chr11:1433042
|
C | CGGGGTCT others(3203): Show |
1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92-2996_92-2995ins others(3210): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433042 | |||||
| chr11:1433044
|
GTCTGGTC others(85): Show |
G | 6 | a0001c0001t0004g0172a0001c0001t0004g0314a0001c0001t0006g0218others(3): Show | 6 | HG01943.hp1 HG01975.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-2995_92-2904del others(92): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433044 | ||||||
| chr11:1433052
|
A | AGGTTTTG others(2445): Show |
1 | a0002c0002t0023g0223 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.92-2972_92-2971ins others(2452): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433052 | |||||
| chr11:1433052
|
A | G | 13 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0186others(10): Show | 14 | HG01109.hp1 HG01261.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.92-2988A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433052 | ||||||
| chr11:1433069
|
T | C | 20 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0186others(17): Show | 21 | HG01070.hp2 HG01109.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.92-2971T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433069 | ||||||
| chr11:1433069
|
T | TCAGCAGT others(980): Show |
1 | a0001c0001t0001g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.92-2960_92-2959ins others(987): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433069 | |||||
| chr11:1433074
|
A | AGTGAGCG others(134): Show |
2 | a0001c0001t0042g0160a0001c0001t0060g0163 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.92-2960_92-2959ins others(141): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433074 | |||||
| chr11:1433074
|
A | G | 14 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0186others(11): Show | 15 | HG01109.hp1 HG01167.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.92-2966A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433074 | ||||||
| chr11:1433081
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.92-2959C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433081 | ||||||
| chr11:1433081
|
C | G | 216 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(213): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.92-2959C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433081 | ||||||
| chr11:1433091
|
GTCTGGTC others(38): Show |
G | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-2948_92-2904del others(45): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433091 | ||||||
| chr11:1433099
|
A | AGGTTTTG others(1311): Show |
1 | a0001c0001t0021g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.92-2925_92-2924ins others(1318): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433099 | |||||
| chr11:1433099
|
A | AGGTTTTG others(1311): Show |
1 | a0001c0001t0003g0288 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.92-2925_92-2924ins others(1318): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433099 | |||||
| chr11:1433099
|
A | AGGTTTTG others(698): Show |
1 | a0002c0002t0010g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.92-2925_92-2924ins others(705): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433099 | |||||
| chr11:1433099
|
A | AGGTTTTG others(228): Show |
2 | a0001c0001t0001g0023a0001c0001t0024g0292 | 2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.92-2925_92-2924ins others(235): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433099 | |||||
| chr11:1433099
|
A | AGGTTTTG others(228): Show |
1 | a0001c0001t0013g0022 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.92-2925_92-2924ins others(235): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433099 | |||||
| chr11:1433099
|
A | G | 20 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0186others(17): Show | 21 | HG01109.hp1 HG01167.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.92-2941A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433099 | ||||||
| chr11:1433116
|
T | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0048others(6): Show | 9 | HG01943.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-2924T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433116 | ||||||
| chr11:1433121
|
A | AGTGAGCG others(228): Show |
1 | a0001c0001t0001g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.92-2880_92-2879ins others(235): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(275): Show |
1 | a0001c0001t0013g0311 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.92-2880_92-2879ins others(282): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(228): Show |
1 | a0002c0002t0005g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.92-2880_92-2879ins others(235): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(322): Show |
1 | a0001c0001t0003g0241 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.92-2880_92-2879ins others(329): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(322): Show |
1 | a0001c0001t0001g0030 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.92-2880_92-2879ins others(329): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(322): Show |
1 | a0001c0001t0001g0011 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.92-2880_92-2879ins others(329): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(369): Show |
1 | a0001c0001t0059g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-2880_92-2879ins others(376): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(369): Show |
1 | a0003c0014t0002g0319 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.92-2880_92-2879ins others(376): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(322): Show |
1 | a0001c0001t0025g0143 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.92-2880_92-2879ins others(329): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(228): Show |
1 | a0001c0001t0011g0303 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.92-2880_92-2879ins others(235): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(275): Show |
1 | a0001c0001t0001g0168 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.92-2880_92-2879ins others(282): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(369): Show |
2 | a0001c0001t0004g0136a0002c0002t0016g0284 | 2 | HG00140.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.92-2880_92-2879ins others(376): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(275): Show |
1 | a0001c0001t0004g0121 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.92-2880_92-2879ins others(282): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(228): Show |
1 | a0001c0001t0001g0317 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.92-2880_92-2879ins others(235): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(275): Show |
1 | a0002c0002t0002g0176 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.92-2895_92-2894ins others(282): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(322): Show |
1 | a0001c0001t0001g0127 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.92-2895_92-2894ins others(329): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(228): Show |
4 | a0001c0001t0003g0220a0001c0001t0021g0206a0001c0001t0021g0221others(1): Show | 4 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-2895_92-2894ins others(235): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(369): Show |
2 | a0002c0002t0023g0254a0002c0002t0023g0255 | 2 | HG03239.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.92-2895_92-2894ins others(376): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(322): Show |
1 | a0001c0001t0001g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.92-2895_92-2894ins others(329): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(463): Show |
1 | a0002c0002t0049g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.92-2895_92-2894ins others(470): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(369): Show |
1 | a0002c0002t0008g0116 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.92-2895_92-2894ins others(376): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | AGTGAGCG others(227): Show |
1 | a0001c0001t0003g0219 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.92-2895_92-2894ins others(234): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433121 | |||||
| chr11:1433121
|
A | G | 25 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(22): Show | 26 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.92-2919A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433121 | ||||||
| chr11:1433128
|
G | C | 1 | a0001c0001t0003g0222 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.92-2912G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433128 | ||||||
| chr11:1433136
|
C | CGG | 24 | a0001c0001t0001g0046a0001c0001t0001g0154a0001c0001t0006g0248others(21): Show | 24 | HG00423.hp1 HG00558.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.92-2903_92-2902dup others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433136 | |||||
| chr11:1433137
|
G | GGTCTGGT others(228): Show |
2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG01943.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.92-2880_92-2879ins others(235): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433137 | |||||
| chr11:1433139
|
T | C | 1 | a0001c0003t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.92-2901T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433139 | ||||||
| chr11:1433146
|
A | G | 2 | a0001c0006t0001g0047a0002c0002t0005g0216 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92-2894A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433146 | ||||||
| chr11:1433198
|
A | G | 162 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(159): Show | 163 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.92-2842A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433198 | ||||||
| chr11:1433257
|
C | T | 114 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(111): Show | 116 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.92-2783C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433257 | ||||||
| chr11:1433295
|
G | A | 4 | a0001c0001t0004g0173a0001c0001t0004g0188a0002c0002t0030g0171others(1): Show | 4 | HG01081.hp1 HG03239.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-2745G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433295 | ||||||
| chr11:1433382
|
C | G | 3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92-2658C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433382 | ||||||
| chr11:1433441
|
T | C | 1 | a0002c0002t0053g0139 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.92-2599T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433441 | ||||||
| chr11:1433445
|
T | C | 254 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(251): Show | 257 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.92-2595T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433445 | ||||||
| chr11:1433458
|
G | A | 20 | a0001c0001t0001g0313a0002c0002t0002g0132a0002c0002t0002g0149others(17): Show | 21 | HG01952.hp2 HG01975.hp2 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.92-2582G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433458 | ||||||
| chr11:1433499
|
C | G | 137 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(134): Show | 138 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.92-2541C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433499 | ||||||
| chr11:1433548
|
C | G | 4 | a0001c0001t0001g0048a0001c0001t0003g0228a0001c0001t0043g0050others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-2492C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433548 | ||||||
| chr11:1433627
|
G | A | 1 | a0007c0013t0004g0065 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.92-2413G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433627 | ||||||
| chr11:1433671
|
C | T | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.92-2369C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433671 | ||||||
| chr11:1433682
|
G | A | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-2358G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433682 | ||||||
| chr11:1433683
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92-2357C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433683 | ||||||
| chr11:1433724
|
T | TCCTCCGG others(23): Show |
1 | a0001c0001t0070g0210 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.92-2314_92-2285dup others(30): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1433724 | |||||
| chr11:1433748
|
C | T | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.92-2292C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433748 | ||||||
| chr11:1433869
|
C | T | 2 | a0001c0001t0006g0229a0001c0001t0006g0248 | 2 | HG02683.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.92-2171C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433869 | ||||||
| chr11:1433903
|
G | A | 1 | a0002c0002t0002g0155 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.92-2137G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433903 | ||||||
| chr11:1433954
|
C | G | 1 | a0002c0002t0015g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.92-2086C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1433954 | ||||||
| chr11:1434021
|
G | A | 3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92-2019G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434021 | ||||||
| chr11:1434040
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.92-2000G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434040 | ||||||
| chr11:1434069
|
A | C | 2 | a0002c0002t0002g0132a0002c0002t0007g0346 | 2 | NA18967.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.92-1971A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434069 | ||||||
| chr11:1434132
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.92-1908C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434132 | ||||||
| chr11:1434206
|
C | T | 3 | a0002c0002t0002g0075a0002c0002t0002g0086a0002c0002t0005g0005 | 4 | NA18995.hp2 NA18999.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-1834C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434206 | ||||||
| chr11:1434218
|
T | C | 1 | a0002c0002t0005g0281 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.92-1822T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434218 | ||||||
| chr11:1434230
|
G | T | 3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92-1810G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434230 | ||||||
| chr11:1434240
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.92-1800C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434240 | ||||||
| chr11:1434337
|
C | CTGGGCCG others(48): Show |
1 | a0002c0002t0030g0174 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92-1641_92-1587dup others(55): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1434337 | |||||
| chr11:1434367
|
T | C | 1 | a0002c0002t0035g0296 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.92-1673T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434367 | ||||||
| chr11:1434379
|
CCCCTGTG others(47): Show |
C | 1 | a0006c0012t0037g0293 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.92-1657_92-1604del others(54): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1434379 | |||||
| chr11:1434457
|
A | C | 1 | a0001c0001t0014g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.92-1583A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434457 | ||||||
| chr11:1434525
|
C | T | 1 | a0001c0001t0003g0288 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.92-1515C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434525 | ||||||
| chr11:1434687
|
G | T | 1 | a0001c0001t0009g0153 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.92-1353G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434687 | ||||||
| chr11:1434786
|
A | G | 1 | a0001c0001t0044g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.92-1254A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434786 | ||||||
| chr11:1434932
|
C | T | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.92-1108C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434932 | ||||||
| chr11:1434933
|
G | T | 1 | a0001c0003t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.92-1107G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434933 | ||||||
| chr11:1434935
|
G | A | 1 | a0001c0003t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.92-1105G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434935 | ||||||
| chr11:1434936
|
C | G | 1 | a0001c0003t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.92-1104C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434936 | ||||||
| chr11:1434937
|
T | C | 1 | a0001c0003t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.92-1103T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434937 | ||||||
| chr11:1434938
|
G | C | 1 | a0001c0003t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.92-1102G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434938 | ||||||
| chr11:1434939
|
T | C | 1 | a0001c0003t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.92-1101T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434939 | ||||||
| chr11:1434945
|
G | C | 1 | a0001c0003t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.92-1095G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434945 | ||||||
| chr11:1434947
|
A | T | 1 | a0001c0003t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.92-1093A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1434947 | ||||||
| chr11:1435081
|
C | G | 1 | a0001c0001t0003g0263 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.92-959C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435081 | ||||||
| chr11:1435198
|
A | G | 1 | a0002c0002t0012g0349 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.92-842A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435198 | ||||||
| chr11:1435206
|
A | AGAGGAGG others(22): Show |
1 | a0001c0001t0003g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.92-816_92-815insAT others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
A | AGAGGAGG others(138): Show |
1 | a0001c0001t0003g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.92-816_92-815insAT others(143): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
A | AGAGGAGG others(51): Show |
7 | a0001c0001t0001g0044a0001c0001t0001g0312a0001c0001t0003g0234others(4): Show | 7 | HG01070.hp2 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-816_92-815insAT others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
A | AGAGGAGG others(109): Show |
1 | a0002c0002t0016g0240 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.92-816_92-815insAT others(114): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
A | AGAGGAGG others(22): Show |
1 | a0001c0001t0076g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.92-808_92-780dupAG others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
A | AGAGGAGG others(51): Show |
3 | a0001c0001t0001g0063a0002c0002t0007g0346a0002c0002t0022g0204 | 3 | HG02004.hp2 NA18940.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.92-787_92-786insAT others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
A | AGAGGAGG others(109): Show |
1 | a0001c0001t0004g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.92-787_92-786insAT others(114): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
A | AGAGGAGG others(109): Show |
1 | a0002c0002t0017g0301 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.92-809_92-808insGG others(114): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
A | AGAGGAGG others(138): Show |
1 | a0002c0002t0007g0308 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.92-809_92-808insGG others(143): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
A | AGAGGAGG others(167): Show |
3 | a0001c0001t0001g0313a0002c0002t0007g0304a0002c0002t0007g0309 | 3 | HG01952.hp2 HG01978.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.92-809_92-808insGG others(172): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
A | AGAGGAGG others(196): Show |
1 | a0002c0002t0007g0294 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.92-809_92-808insGG others(201): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
A | AGAGGAGG others(370): Show |
1 | a0002c0002t0035g0296 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.92-809_92-808insGG others(375): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
A | AGAGGAGG others(80): Show |
1 | a0002c0002t0050g0165 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.92-809_92-808insGG others(85): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
AGAGGAGG others(22): Show |
A | 5 | a0001c0001t0062g0257a0001c0003t0001g0135a0001c0003t0001g0331others(2): Show | 5 | HG00673.hp1 HG02129.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-808_92-780delAG others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
AGAGGAGG others(51): Show |
A | 2 | a0001c0001t0003g0270a0002c0017t0052g0008 | 2 | HG01433.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.92-808_92-751delAG others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
AGAGGAGG others(80): Show |
A | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG01943.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.92-808_92-722delAG others(85): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
AGAGGAGG others(138): Show |
A | 7 | a0001c0003t0001g0138a0001c0003t0001g0335a0001c0003t0001g0336others(4): Show | 7 | HG00558.hp1 NA18955.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-808_92-664del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
AGAGGAGG others(167): Show |
A | 3 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0134 | 3 | HG00423.hp1 NA18970.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.92-808_92-635del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435206
|
AGAGGAGG others(225): Show |
A | 7 | a0001c0004t0001g0091a0001c0004t0001g0093a0001c0004t0001g0094others(4): Show | 7 | HG01433.hp1 NA18940.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-808_92-577del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435206 | |||||
| chr11:1435225
|
G | A | 4 | a0001c0001t0003g0232a0001c0001t0003g0235a0001c0001t0044g0016others(1): Show | 4 | HG02922.hp2 HG02976.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-815G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435225 | ||||||
| chr11:1435226
|
G | GGGTCTCA others(23): Show |
1 | a0002c0002t0038g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.92-813_92-812insGT others(28): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435226 | |||||
| chr11:1435226
|
G | GGTCTCAG others(22): Show |
11 | a0001c0001t0001g0069a0001c0001t0001g0123a0001c0001t0001g0124others(8): Show | 11 | HG00609.hp1 HG00639.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-787_92-786insAT others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435226 | |||||
| chr11:1435226
|
G | GGTCTCAG others(138): Show |
1 | a0001c0001t0001g0127 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.92-787_92-786insAT others(143): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435226 | |||||
| chr11:1435226
|
G | GGTCTCAG others(51): Show |
1 | a0002c0002t0005g0258 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.92-780_92-779insAG others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435226 | |||||
| chr11:1435226
|
G | T | 4 | a0001c0001t0003g0232a0001c0001t0003g0235a0001c0001t0044g0016others(1): Show | 4 | HG02922.hp2 HG02976.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-814G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435226 | ||||||
| chr11:1435232
|
A | AGCGGAGG others(196): Show |
1 | a0002c0002t0023g0223 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.92-788_92-787insCA others(201): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(138): Show |
1 | a0001c0001t0001g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.92-788_92-787insCA others(143): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(80): Show |
1 | a0002c0002t0016g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.92-788_92-787insCA others(85): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(807): Show |
1 | a0001c0001t0003g0268 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.92-788_92-787insCA others(812): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(80): Show |
12 | a0002c0002t0002g0132a0002c0002t0002g0149a0002c0002t0005g0211others(9): Show | 14 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.92-787_92-786insAT others(85): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(138): Show |
1 | a0002c0002t0005g0283 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.92-787_92-786insAT others(143): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(399): Show |
1 | a0001c0001t0003g0196 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.92-787_92-786insAT others(404): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(428): Show |
1 | a0001c0001t0003g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-787_92-786insAT others(433): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(51): Show |
4 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0004g0106others(1): Show | 4 | HG01256.hp1 HG02293.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-787_92-786insAT others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(80): Show |
2 | a0001c0001t0001g0058a0002c0002t0012g0347 | 2 | HG04228.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.92-787_92-786insAT others(85): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(167): Show |
1 | a0002c0002t0023g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.92-787_92-786insAT others(172): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(312): Show |
1 | a0002c0002t0023g0254 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.92-787_92-786insAT others(317): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(138): Show |
3 | a0001c0001t0001g0102a0002c0002t0017g0353a0002c0002t0066g0285 | 3 | HG03492.hp1 NA18975.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.92-787_92-786insAT others(143): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(225): Show |
1 | a0002c0002t0033g0286 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.92-787_92-786insAT others(230): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(283): Show |
1 | a0001c0001t0001g0329 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.92-787_92-786insAT others(288): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(312): Show |
1 | a0002c0002t0015g0327 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.92-787_92-786insAT others(317): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(370): Show |
1 | a0001c0001t0001g0328 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.92-787_92-786insAT others(375): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(573): Show |
1 | a0001c0001t0009g0101 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.92-787_92-786insAT others(578): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(109): Show |
1 | a0002c0008t0002g0326 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.92-787_92-786insAT others(114): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(283): Show |
1 | a0002c0002t0019g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92-787_92-786insAT others(288): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(51): Show |
1 | a0001c0001t0003g0227 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.92-787_92-786insAT others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(80): Show |
1 | a0002c0002t0008g0071 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.92-787_92-786insAT others(85): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(22): Show |
3 | a0001c0001t0003g0200a0001c0001t0003g0201a0003c0014t0002g0319 | 3 | HG02559.hp2 HG03516.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.92-787_92-786insAT others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(515): Show |
1 | a0002c0011t0002g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.92-787_92-786insAT others(520): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(283): Show |
1 | a0002c0002t0002g0126 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.92-787_92-786insAT others(288): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(167): Show |
1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.92-780_92-779insAG others(172): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(51): Show |
1 | a0001c0006t0027g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.92-780_92-779insAG others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(22): Show |
2 | a0001c0001t0043g0050a0002c0002t0005g0259 | 2 | HG02132.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.92-474_92-446dupCC others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(140): Show |
1 | a0001c0001t0006g0218 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.92-755_92-754insGT others(145): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(51): Show |
1 | a0001c0001t0004g0177 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.92-503_92-446dupCC others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(109): Show |
2 | a0002c0002t0005g0262a0002c0002t0041g0144 | 2 | NA18967.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.92-561_92-446dupCC others(114): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(138): Show |
1 | a0002c0002t0002g0152 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.92-590_92-446dupCC others(143): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(370): Show |
1 | a0001c0001t0001g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.92-620_92-619insTC others(375): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | AGCGGAGG others(135): Show |
1 | a0001c0001t0003g0219 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.92-797_92-796insTG others(140): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
A | G | 19 | a0001c0001t0001g0044a0001c0001t0001g0312a0001c0001t0001g0313others(16): Show | 19 | HG00544.hp2 HG00642.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.92-808A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435232 | ||||||
| chr11:1435232
|
AGCGGAGG others(22): Show |
A | 37 | a0001c0001t0001g0030a0001c0001t0001g0048a0001c0001t0001g0057others(34): Show | 37 | HG00323.hp1 HG00323.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.92-474_92-446delCC others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
AGCGGAGG others(51): Show |
A | 28 | a0001c0001t0001g0072a0001c0001t0001g0154a0001c0001t0003g0193others(25): Show | 28 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.92-503_92-446delCC others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
AGCGGAGG others(80): Show |
A | 38 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0087others(35): Show | 40 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.92-532_92-446delCC others(85): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
AGCGGAGG others(109): Show |
A | 8 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0186others(5): Show | 8 | HG00408.hp1 HG00544.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-561_92-446del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
AGCGGAGG others(138): Show |
A | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG01361.hp2 HG01496.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-590_92-446del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
AGCGGAGG others(167): Show |
A | 4 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0004g0180others(1): Show | 4 | HG00438.hp2 HG01993.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-619_92-446del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
AGCGGAGG others(196): Show |
A | 5 | a0001c0001t0003g0228a0001c0001t0004g0175a0001c0001t0018g0137others(2): Show | 5 | HG01261.hp2 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-648_92-446del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
AGCGGAGG others(225): Show |
A | 1 | a0001c0001t0047g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.92-677_92-446del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435232
|
AGCGGAGG others(312): Show |
A | 2 | a0002c0005t0034g0055a0002c0005t0034g0056 | 2 | HG01346.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.92-764_92-446del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435232 | |||||
| chr11:1435239
|
G | GAGGGGTG others(22): Show |
2 | a0001c0001t0003g0203a0001c0001t0003g0239 | 2 | HG00741.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.92-787_92-786insAT others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435239 | |||||
| chr11:1435240
|
A | AGGGGTGC others(81): Show |
1 | a0002c0002t0008g0116 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.92-788_92-787insCA others(86): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435240 | |||||
| chr11:1435241
|
GGGGTGCC others(137): Show |
G | 1 | a0001c0001t0014g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.92-795_92-652del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435241 | |||||
| chr11:1435242
|
GGGTGCCG others(49): Show |
G | 1 | a0002c0002t0002g0159 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.92-795_92-740delTG others(54): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435242 | |||||
| chr11:1435251
|
T | TGGATGTC others(81): Show |
1 | a0002c0002t0007g0345 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.92-787_92-786insAT others(86): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435251 | |||||
| chr11:1435253
|
G | C | 2 | a0002c0002t0010g0246a0002c0002t0049g0117 | 2 | HG01891.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.92-787G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435253 | ||||||
| chr11:1435254
|
G | A | 38 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0029others(35): Show | 39 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.92-786G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435254 | ||||||
| chr11:1435255
|
G | GGTCTCAG others(1095): Show |
1 | a0001c0001t0044g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.92-780_92-779insAG others(1100): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435255 | |||||
| chr11:1435255
|
G | T | 38 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0029others(35): Show | 39 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.92-785G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435255 | ||||||
| chr11:1435261
|
G | A | 51 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0029others(48): Show | 52 | HG00140.hp1 HG00609.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.92-779G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435261 | ||||||
| chr11:1435268
|
G | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0029others(9): Show | 13 | HG00609.hp2 HG00735.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-772G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435268 | ||||||
| chr11:1435281
|
GGGGGTCT others(108): Show |
G | 1 | a0006c0012t0037g0293 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.92-754_92-640del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435281 | |||||
| chr11:1435283
|
G | A | 31 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0066others(28): Show | 31 | HG00323.hp1 HG01109.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.92-757G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435283 | ||||||
| chr11:1435284
|
G | T | 28 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0066others(25): Show | 28 | HG00323.hp1 HG01109.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.92-756G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435284 | ||||||
| chr11:1435290
|
G | A | 56 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0029others(53): Show | 57 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.92-750G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435290 | ||||||
| chr11:1435297
|
G | T | 3 | a0001c0001t0001g0030a0001c0001t0031g0012a0002c0002t0019g0043 | 3 | HG03098.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.92-743G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435297 | ||||||
| chr11:1435305
|
C | CCGGTGGG others(631): Show |
1 | a0001c0001t0001g0191 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.92-446_92-445insCC others(636): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435305 | |||||
| chr11:1435305
|
C | T | 2 | a0001c0001t0003g0220a0001c0001t0004g0172 | 2 | HG01516.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.92-735C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435305 | ||||||
| chr11:1435310
|
GGGGGTCT others(79): Show |
G | 1 | a0007c0013t0004g0065 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.92-725_92-640delTC others(84): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435310 | |||||
| chr11:1435310
|
GGGGGTCT others(137): Show |
G | 1 | a0001c0003t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.92-725_92-582del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435310 | |||||
| chr11:1435312
|
G | A | 22 | a0001c0001t0001g0150a0001c0001t0003g0193a0001c0001t0003g0263others(19): Show | 22 | HG00280.hp2 HG00609.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.92-728G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435312 | ||||||
| chr11:1435313
|
G | T | 20 | a0001c0001t0001g0150a0001c0001t0003g0193a0001c0001t0003g0263others(17): Show | 20 | HG00280.hp2 HG00609.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-727G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435313 | ||||||
| chr11:1435319
|
G | A | 33 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0034others(30): Show | 33 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.92-721G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435319 | ||||||
| chr11:1435319
|
G | GGCGGAGG others(167): Show |
1 | a0001c0001t0001g0067 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.92-635_92-634insAG others(172): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435319 | |||||
| chr11:1435326
|
G | T | 2 | a0002c0002t0019g0042a0002c0008t0005g0278 | 2 | HG01884.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.92-714G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435326 | ||||||
| chr11:1435334
|
C | T | 1 | a0001c0001t0003g0219 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.92-706C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435334 | ||||||
| chr11:1435339
|
GGGGGTCT others(137): Show |
G | 1 | a0001c0001t0006g0215 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.92-696_92-553del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435339 | |||||
| chr11:1435341
|
G | A | 30 | a0001c0001t0001g0034a0001c0001t0001g0049a0001c0001t0001g0052others(27): Show | 32 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.92-699G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435341 | ||||||
| chr11:1435342
|
G | T | 30 | a0001c0001t0001g0034a0001c0001t0001g0049a0001c0001t0001g0052others(27): Show | 32 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.92-698G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435342 | ||||||
| chr11:1435348
|
G | A | 38 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0034others(35): Show | 40 | HG00280.hp1 HG00741.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.92-692G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435348 | ||||||
| chr11:1435355
|
G | GAGGGGTG others(51): Show |
1 | a0001c0001t0003g0239 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.92-642_92-641insAT others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435355 | |||||
| chr11:1435355
|
G | T | 18 | a0001c0001t0001g0049a0001c0001t0001g0087a0001c0001t0001g0107others(15): Show | 20 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-685G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435355 | ||||||
| chr11:1435356
|
A | AGGGGTGC others(110): Show |
1 | a0001c0001t0001g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.92-584_92-583insAT others(115): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435356 | |||||
| chr11:1435370
|
G | A | 8 | a0001c0001t0001g0058a0001c0001t0001g0109a0001c0001t0001g0110others(5): Show | 8 | HG00408.hp1 HG00544.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-670G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435370 | ||||||
| chr11:1435371
|
G | T | 8 | a0001c0001t0001g0058a0001c0001t0001g0109a0001c0001t0001g0110others(5): Show | 8 | HG00408.hp1 HG00544.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-669G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435371 | ||||||
| chr11:1435377
|
G | A | 13 | a0001c0001t0001g0030a0001c0001t0001g0109a0001c0001t0001g0110others(10): Show | 14 | HG00408.hp1 HG00544.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.92-663G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435377 | ||||||
| chr11:1435384
|
G | GAGGGGTG others(22): Show |
1 | a0001c0001t0063g0253 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.92-628_92-627insTA others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435384 | |||||
| chr11:1435384
|
G | T | 1 | a0001c0001t0013g0311 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.92-656G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435384 | ||||||
| chr11:1435392
|
C | CCGGTGGG others(51): Show |
1 | a0001c0001t0048g0342 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.92-591_92-590insTC others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435392 | |||||
| chr11:1435392
|
C | T | 1 | a0002c0002t0005g0283 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.92-648C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435392 | ||||||
| chr11:1435396
|
TGGGGGTC others(110): Show |
T | 1 | a0001c0001t0003g0288 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.92-639_92-523del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435396 | |||||
| chr11:1435397
|
GGGGGTCT others(79): Show |
G | 1 | a0002c0002t0002g0060 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.92-638_92-553delTC others(84): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435397 | |||||
| chr11:1435399
|
G | A | 5 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0339others(2): Show | 5 | HG01192.hp1 HG01496.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-641G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435399 | ||||||
| chr11:1435400
|
G | T | 5 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0339others(2): Show | 5 | HG01192.hp1 HG01496.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-640G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435400 | ||||||
| chr11:1435406
|
G | A | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 17 | HG00735.hp2 HG01192.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.92-634G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435406 | ||||||
| chr11:1435413
|
G | T | 1 | a0002c0002t0005g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.92-627G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435413 | ||||||
| chr11:1435415
|
GGGGTGCC others(79): Show |
G | 1 | a0001c0001t0013g0022 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.92-621_92-536delTG others(84): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435415 | |||||
| chr11:1435421
|
C | CCGGTGGG others(109): Show |
1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-591_92-590insTC others(114): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435421 | |||||
| chr11:1435421
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.92-619C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435421 | ||||||
| chr11:1435423
|
G | GGTGGGGG others(49): Show |
1 | a0001c0001t0003g0219 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.92-576_92-575insCG others(54): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435423 | |||||
| chr11:1435428
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0003g0268others(1): Show | 4 | HG00438.hp2 HG00621.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-612G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435428 | ||||||
| chr11:1435429
|
G | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0003g0268others(1): Show | 4 | HG00438.hp2 HG00621.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-611G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435429 | ||||||
| chr11:1435435
|
G | A | 9 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0003g0227others(6): Show | 10 | HG00438.hp2 HG01192.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-605G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435435 | ||||||
| chr11:1435440
|
AGGAGGGG others(81): Show |
A | 1 | a0001c0001t0070g0210 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.92-598_92-511delGA others(86): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435440 | |||||
| chr11:1435444
|
G | A | 2 | a0001c0003t0014g0037a0001c0003t0014g0038 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.92-596G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435444 | ||||||
| chr11:1435450
|
C | CCGGTGGG others(80): Show |
1 | a0001c0001t0057g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.92-504_92-503insTC others(85): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435450 | |||||
| chr11:1435450
|
C | T | 4 | a0001c0001t0001g0317a0001c0001t0068g0243a0002c0002t0005g0211others(1): Show | 4 | HG01255.hp2 HG01975.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-590C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435450 | ||||||
| chr11:1435450
|
CCGGTGGG others(138): Show |
C | 2 | a0001c0003t0001g0135a0001c0003t0001g0331 | 2 | HG00673.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.92-568_92-424del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435450 | |||||
| chr11:1435454
|
T | TGGGGGGT others(53): Show |
1 | a0001c0001t0068g0243 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.92-581_92-580insGT others(58): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435454 | |||||
| chr11:1435457
|
G | A | 2 | a0002c0007t0010g0244a0002c0007t0010g0245 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.92-583G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435457 | ||||||
| chr11:1435458
|
G | T | 2 | a0002c0007t0010g0244a0002c0007t0010g0245 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.92-582G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435458 | ||||||
| chr11:1435464
|
G | A | 7 | a0001c0001t0003g0227a0001c0001t0014g0039a0001c0001t0018g0137others(4): Show | 7 | HG01192.hp1 HG01261.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-576G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435464 | ||||||
| chr11:1435471
|
G | T | 2 | a0002c0007t0010g0244a0002c0007t0010g0245 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.92-569G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435471 | ||||||
| chr11:1435479
|
C | CCGGTGGG others(22): Show |
2 | a0001c0001t0001g0127a0001c0001t0003g0220 | 2 | HG01516.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.92-533_92-532insTC others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435479 | |||||
| chr11:1435479
|
C | T | 32 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0313others(29): Show | 34 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.92-561C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435479 | ||||||
| chr11:1435481
|
G | A | 1 | a0002c0002t0002g0103 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.92-559G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435481 | ||||||
| chr11:1435486
|
G | A | 1 | a0001c0001t0047g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.92-554G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435486 | ||||||
| chr11:1435487
|
G | T | 1 | a0001c0001t0047g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.92-553G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435487 | ||||||
| chr11:1435493
|
G | A | 2 | a0001c0001t0018g0137a0001c0001t0045g0040 | 2 | HG01261.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.92-547G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435493 | ||||||
| chr11:1435495
|
C | T | 2 | a0002c0002t0002g0155a0002c0002t0017g0353 | 2 | NA18944.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.92-545C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435495 | ||||||
| chr11:1435500
|
G | C | 1 | a0001c0001t0006g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.92-540G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435500 | ||||||
| chr11:1435508
|
C | CCGGTGGG others(196): Show |
1 | a0001c0001t0004g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.92-446_92-445insCC others(201): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435508 | |||||
| chr11:1435508
|
C | CCGGTGGG others(254): Show |
1 | a0002c0002t0005g0005 | 2 | NA18995.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.92-424_92-423insAG others(259): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435508 | |||||
| chr11:1435508
|
C | CCGGTGGG others(22): Show |
1 | a0001c0001t0004g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.92-504_92-503insTC others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435508 | |||||
| chr11:1435508
|
C | T | 7 | a0001c0001t0025g0143a0001c0001t0074g0213a0002c0002t0005g0260others(4): Show | 7 | HG01255.hp1 HG01346.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-532C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435508 | ||||||
| chr11:1435508
|
CCGGTGGG others(80): Show |
C | 3 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0006g0247 | 3 | HG01175.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.92-510_92-424delAG others(85): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435508 | |||||
| chr11:1435525
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.92-515G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435525 | ||||||
| chr11:1435537
|
C | CCGGTGGG others(51): Show |
1 | a0002c0002t0002g0126 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.92-481_92-424dupAG others(56): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435537 | |||||
| chr11:1435537
|
C | CCGGTGGG others(22): Show |
1 | a0002c0002t0010g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.92-475_92-474insTC others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435537 | |||||
| chr11:1435537
|
C | T | 3 | a0001c0001t0001g0046a0001c0001t0013g0022a0001c0001t0031g0012 | 3 | HG02809.hp2 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.92-503C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435537 | ||||||
| chr11:1435551
|
G | A | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0024g0299others(3): Show | 7 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-489G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435551 | ||||||
| chr11:1435553
|
C | T | 2 | a0001c0001t0004g0175a0001c0001t0059g0041 | 2 | HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.92-487C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435553 | ||||||
| chr11:1435554
|
G | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0009g0187 | 3 | NA18939.hp2 NA18940.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.92-486G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435554 | ||||||
| chr11:1435560
|
GGGGTGCC others(21): Show |
G | 1 | a0001c0001t0001g0099 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.92-476_92-449delTG others(26): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435560 | |||||
| chr11:1435566
|
C | CCGGTGGG others(22): Show |
1 | a0002c0002t0002g0086 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.92-452_92-424dupAG others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435566 | |||||
| chr11:1435573
|
G | A | 1 | a0001c0001t0059g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-467G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435573 | ||||||
| chr11:1435574
|
G | T | 1 | a0001c0001t0059g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-466G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435574 | ||||||
| chr11:1435580
|
G | A | 11 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0003g0227others(8): Show | 11 | HG01346.hp1 HG01516.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.92-460G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435580 | ||||||
| chr11:1435595
|
T | C | 5 | a0001c0001t0001g0328a0001c0001t0003g0002a0001c0001t0003g0045others(2): Show | 6 | HG01516.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-445T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435595 | ||||||
| chr11:1435661
|
C | G | 1 | a0002c0002t0002g0323 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.92-379C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435661 | ||||||
| chr11:1435673
|
C | CG | 5 | a0001c0001t0003g0263a0001c0001t0004g0081a0002c0002t0002g0060others(2): Show | 5 | HG00738.hp1 NA18977.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-362dupG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 1435673 | |||||
| chr11:1435684
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.92-356C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435684 | ||||||
| chr11:1435978
|
C | T | 1 | a0001c0001t0045g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.92-62C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1435978 | ||||||
| chr11:1436008
|
T | C | 30 | a0001c0001t0001g0046a0001c0003t0001g0070a0001c0003t0001g0114others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.92-32T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1436008 | ||||||
| chr11:1436037
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp2 | splice_region_variant&intron_variant | LOW | c.92-3C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | 1436037 | ||||||
| chr11:1436223
|
C | T | 2 | a0001c0001t0001g0343a0001c0001t0047g0340 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.186+89C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436223 | ||||||
| chr11:1436242
|
G | C | 53 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 54 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.186+108G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436242 | ||||||
| chr11:1436251
|
C | T | 31 | a0001c0001t0001g0046a0001c0003t0001g0070a0001c0003t0001g0114others(28): Show | 31 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.186+117C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436251 | ||||||
| chr11:1436288
|
C | T | 1 | a0001c0001t0004g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.186+154C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436288 | ||||||
| chr11:1436309
|
C | T | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.186+175C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436309 | ||||||
| chr11:1436322
|
C | A | 1 | a0001c0001t0011g0303 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.186+188C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436322 | ||||||
| chr11:1436378
|
A | G | 2 | a0001c0006t0001g0047a0001c0006t0027g0142 | 2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.186+244A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436378 | ||||||
| chr11:1436424
|
C | A | 1 | a0002c0002t0005g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.186+290C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436424 | ||||||
| chr11:1436428
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.186+294C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436428 | ||||||
| chr11:1436547
|
C | T | 1 | a0001c0001t0003g0239 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.186+413C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436547 | ||||||
| chr11:1436606
|
G | A | 5 | a0001c0001t0031g0012a0001c0001t0032g0195a0001c0001t0032g0209others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.186+472G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436606 | ||||||
| chr11:1436639
|
G | C | 3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.186+505G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436639 | ||||||
| chr11:1436651
|
C | T | 1 | a0002c0002t0050g0165 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.186+517C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436651 | ||||||
| chr11:1436658
|
G | A | 2 | a0001c0001t0004g0175a0001c0001t0004g0180 | 2 | HG01993.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.186+524G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436658 | ||||||
| chr11:1436687
|
G | A | 2 | a0001c0001t0003g0287a0001c0001t0062g0257 | 2 | HG02486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.186+553G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436687 | ||||||
| chr11:1436705
|
C | G | 1 | a0001c0001t0078g0205 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.186+571C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436705 | ||||||
| chr11:1436773
|
G | A | 1 | a0002c0002t0008g0151 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.186+639G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436773 | ||||||
| chr11:1436817
|
G | C | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.186+683G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436817 | ||||||
| chr11:1436847
|
C | T | 4 | a0001c0003t0014g0036a0001c0003t0014g0037a0001c0003t0014g0038others(1): Show | 4 | HG00642.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.186+713C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436847 | ||||||
| chr11:1436901
|
A | G | 252 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(249): Show | 255 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.186+767A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436901 | ||||||
| chr11:1436953
|
G | A | 1 | a0001c0001t0003g0193 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.186+819G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1436953 | ||||||
| chr11:1437016
|
G | A | 1 | a0002c0002t0002g0323 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.186+882G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1437016 | ||||||
| chr11:1437130
|
C | T | 85 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(82): Show | 87 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.186+996C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1437130 | ||||||
| chr11:1437221
|
G | T | 1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.187-1085G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1437221 | ||||||
| chr11:1437294
|
A | G | 2 | a0002c0005t0034g0055a0002c0005t0034g0056 | 2 | HG01346.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.187-1012A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1437294 | ||||||
| chr11:1437298
|
G | A | 2 | a0001c0003t0014g0037a0001c0003t0014g0038 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.187-1008G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1437298 | ||||||
| chr11:1437315
|
A | G | 1 | a0002c0002t0008g0071 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.187-991A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1437315 | ||||||
| chr11:1437345
|
G | T | 1 | a0001c0001t0070g0210 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187-961G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1437345 | ||||||
| chr11:1437351
|
C | T | 3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.187-955C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1437351 | ||||||
| chr11:1437492
|
C | T | 85 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(82): Show | 87 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.187-814C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1437492 | ||||||
| chr11:1437604
|
C | T | 1 | a0002c0002t0002g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.187-702C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1437604 | ||||||
| chr11:1437721
|
C | T | 97 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(94): Show | 98 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.187-585C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1437721 | ||||||
| chr11:1437864
|
C | A | 25 | a0001c0001t0001g0154a0001c0001t0001g0189a0001c0001t0001g0191others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.187-442C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1437864 | ||||||
| chr11:1438027
|
A | ATCCCCCA others(24): Show |
4 | a0001c0003t0004g0290a0002c0002t0058g0325a0002c0005t0034g0055others(1): Show | 4 | HG01346.hp2 HG02280.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.187-154_187-124dup others(31): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | 1438027 | |||||
| chr11:1438027
|
A | ATCCCCCA others(55): Show |
2 | a0002c0002t0033g0286a0002c0002t0066g0285 | 2 | HG02738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.187-185_187-124dup others(62): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | 1438027 | |||||
| chr11:1438027
|
A | G | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.187-279A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | chr11 | 1438027 | ||||||
| chr11:1438027
|
ATCCCCCA others(24): Show |
A | 34 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0099others(31): Show | 34 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.187-154_187-124del others(31): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | 1438027 | |||||
| chr11:1438027
|
ATCCCCCA others(55): Show |
A | 1 | a0002c0002t0002g0079 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.187-185_187-124del others(62): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | 1438027 | |||||
| chr11:1438059
|
TCCCCCAC others(117): Show |
T | 1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.187-216_187-93del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | 1438059 | |||||
| chr11:1438060
|
CCCCCACA others(23): Show |
C | 1 | a0001c0001t0068g0243 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.187-241_187-212del others(30): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | 1438060 | |||||
| chr11:1438090
|
T | TCCCCCAC others(179): Show |
1 | a0002c0002t0069g0231 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.187-69_187-68insCC others(184): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | 1438090 | |||||
| chr11:1438090
|
TCCCCCAC others(86): Show |
T | 1 | a0002c0011t0002g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.187-185_187-93delT others(92): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | 1438090 | |||||
| chr11:1438152
|
TCCCCCAC others(24): Show |
T | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.187-99_187-69delCC others(29): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | 1438152 | |||||
| chr11:1438421
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.272+30G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1438421 | ||||||
| chr11:1438428
|
A | AG | 3 | a0001c0001t0001g0099a0001c0001t0003g0263a0001c0001t0070g0210 | 3 | HG02895.hp1 NA18994.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.272+39dupG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr11 | 1438428 | |||||
| chr11:1438469
|
G | C | 104 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(101): Show | 105 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.272+78G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1438469 | ||||||
| chr11:1438653
|
C | T | 2 | a0002c0005t0034g0055a0002c0005t0034g0056 | 2 | HG01346.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.272+262C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1438653 | ||||||
| chr11:1438744
|
T | G | 2 | a0002c0002t0002g0103a0002c0002t0005g0269 | 2 | HG02132.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.272+353T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1438744 | ||||||
| chr11:1438753
|
C | T | 2 | a0002c0007t0010g0244a0002c0007t0010g0245 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.272+362C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1438753 | ||||||
| chr11:1438806
|
C | T | 6 | a0001c0001t0001g0141a0002c0002t0008g0116a0002c0002t0010g0246others(3): Show | 6 | HG01099.hp1 HG01167.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.272+415C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1438806 | ||||||
| chr11:1438853
|
G | A | 1 | a0002c0002t0005g0211 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.272+462G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1438853 | ||||||
| chr11:1438879
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.272+488C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1438879 | ||||||
| chr11:1438981
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.272+590G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1438981 | ||||||
| chr11:1438988
|
C | CA | 3 | a0001c0001t0003g0002a0001c0001t0003g0045a0001c0001t0003g0203 | 4 | HG02572.hp1 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.272+598dupA | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr11 | 1438988 | |||||
| chr11:1439122
|
T | C | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.272+731T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1439122 | ||||||
| chr11:1439145
|
A | G | 7 | a0002c0002t0005g0211a0002c0002t0005g0260a0002c0002t0005g0281others(4): Show | 7 | HG01346.hp1 HG01934.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.272+754A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1439145 | ||||||
| chr11:1439242
|
C | T | 1 | a0001c0001t0018g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.272+851C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1439242 | ||||||
| chr11:1439289
|
C | T | 2 | a0002c0002t0015g0028a0002c0002t0015g0330 | 2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.272+898C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1439289 | ||||||
| chr11:1439347
|
T | G | 61 | a0001c0001t0001g0049a0001c0001t0001g0087a0001c0001t0001g0107others(58): Show | 62 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.272+956T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1439347 | ||||||
| chr11:1439409
|
A | C | 251 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(248): Show | 254 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.272+1018A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1439409 | ||||||
| chr11:1439419
|
C | T | 1 | a0002c0002t0002g0323 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.272+1028C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1439419 | ||||||
| chr11:1439594
|
C | G | 1 | a0001c0001t0004g0316 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.273-1194C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1439594 | ||||||
| chr11:1439780
|
AGGGCTTC others(19): Show |
A | 1 | a0001c0001t0004g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.273-995_273-970del others(26): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr11 | 1439780 | |||||
| chr11:1439843
|
CCTTCCCC others(19): Show |
C | 1 | a0001c0001t0003g0227 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.273-921_273-896del others(26): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr11 | 1439843 | |||||
| chr11:1439847
|
C | T | 1 | a0001c0001t0006g0218 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.273-941C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1439847 | ||||||
| chr11:1439869
|
T | TCTTCCCC others(20): Show |
4 | a0001c0003t0003g0291a0002c0005t0005g0289a0002c0005t0034g0055others(1): Show | 4 | HG01346.hp2 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-895_273-894ins others(27): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr11 | 1439869 | |||||
| chr11:1440105
|
C | A | 3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.273-683C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1440105 | ||||||
| chr11:1440106
|
C | G | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.273-682C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1440106 | ||||||
| chr11:1440145
|
C | T | 2 | a0001c0001t0006g0215a0001c0001t0074g0213 | 2 | HG01261.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.273-643C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1440145 | ||||||
| chr11:1440150
|
T | C | 1 | a0001c0001t0011g0295 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.273-638T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1440150 | ||||||
| chr11:1440218
|
G | A | 4 | a0001c0003t0003g0291a0002c0005t0005g0289a0002c0005t0034g0055others(1): Show | 4 | HG01346.hp2 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-570G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1440218 | ||||||
| chr11:1440223
|
C | T | 30 | a0001c0001t0001g0049a0001c0001t0001g0087a0001c0001t0001g0107others(27): Show | 31 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.273-565C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1440223 | ||||||
| chr11:1440282
|
C | G | 6 | a0001c0001t0001g0313a0002c0002t0007g0294a0002c0002t0007g0304others(3): Show | 6 | HG01952.hp2 HG01975.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.273-506C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1440282 | ||||||
| chr11:1440331
|
G | A | 2 | a0001c0001t0042g0160a0001c0001t0060g0163 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.273-457G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1440331 | ||||||
| chr11:1440450
|
G | T | 1 | a0002c0002t0005g0269 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.273-338G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1440450 | ||||||
| chr11:1440470
|
G | A | 1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.273-318G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1440470 | ||||||
| chr11:1440532
|
C | T | 1 | a0002c0002t0015g0027 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.273-256C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1440532 | ||||||
| chr11:1440753
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.273-35A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 3/19 | chr11 | 1440753 | ||||||
| chr11:1440932
|
AG | A | 117 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(114): Show | 119 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
splice_region_variant&intron_variant | LOW | c.413+6delG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1440932 | |||||
| chr11:1440982
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02055.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.413+54C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1440982 | ||||||
| chr11:1440987
|
C | T | 83 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(80): Show | 85 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.413+59C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1440987 | ||||||
| chr11:1441023
|
C | G | 2 | a0001c0001t0028g0332a0001c0001t0028g0333 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.413+95C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441023 | ||||||
| chr11:1441052
|
CCCCCATT others(30): Show |
C | 1 | a0001c0003t0014g0038 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.413+151_413+187del others(37): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441052 | |||||
| chr11:1441116
|
T | C | 106 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(103): Show | 107 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.413+188T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441116 | ||||||
| chr11:1441133
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.413+205A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441133 | ||||||
| chr11:1441150
|
T | TCCCCCCA others(151): Show |
1 | a0001c0001t0003g0241 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.413+345_413+346ins others(158): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441150 | |||||
| chr11:1441163
|
T | G | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.413+235T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441163 | ||||||
| chr11:1441180
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.413+252G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441180 | ||||||
| chr11:1441223
|
A | ACTACCCC others(25): Show |
2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG01943.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.413+313_413+314ins others(32): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441223 | |||||
| chr11:1441223
|
ACTACCCC others(284): Show |
A | 2 | a0001c0001t0001g0082a0001c0001t0001g0097 | 2 | NA19005.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.413+318_413+608del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441223 | |||||
| chr11:1441248
|
C | A | 1 | a0002c0002t0005g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.413+320C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441248 | ||||||
| chr11:1441248
|
C | T | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+320C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441248 | ||||||
| chr11:1441257
|
G | T | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+329G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441257 | ||||||
| chr11:1441258
|
G | A | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+330G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441258 | ||||||
| chr11:1441274
|
C | G | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+346C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441274 | ||||||
| chr11:1441274
|
C | T | 1 | a0002c0002t0002g0323 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.413+346C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441274 | ||||||
| chr11:1441289
|
T | TGCCCCTC others(88): Show |
1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+443_413+444ins others(95): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441289 | |||||
| chr11:1441289
|
T | TGCCCCTC others(249): Show |
1 | a0002c0002t0005g0274 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.413+576_413+577ins others(256): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441289 | |||||
| chr11:1441290
|
GC | G | 25 | a0001c0001t0001g0154a0001c0001t0001g0189a0001c0001t0001g0191others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.413+366delC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441290 | |||||
| chr11:1441290
|
GCCCCTCA others(25): Show |
G | 1 | a0002c0002t0005g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.413+391_413+422del others(32): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441290 | |||||
| chr11:1441291
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.413+363C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441291 | ||||||
| chr11:1441292
|
C | G | 25 | a0001c0001t0001g0154a0001c0001t0001g0189a0001c0001t0001g0191others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.413+364C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441292 | ||||||
| chr11:1441306
|
A | G | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+378A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441306 | ||||||
| chr11:1441313
|
CCATTAAC others(158): Show |
C | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+386_413+550del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441313 | ||||||
| chr11:1441330
|
A | G | 1 | a0002c0002t0002g0152 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.413+402A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441330 | ||||||
| chr11:1441353
|
G | GGCCCCTC others(25): Show |
1 | a0002c0002t0030g0171 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.413+441_413+472dup others(32): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441353 | |||||
| chr11:1441369
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0048others(3): Show | 6 | HG02145.hp2 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+441C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441369 | ||||||
| chr11:1441371
|
T | C | 1 | a0001c0001t0064g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.413+443T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441371 | ||||||
| chr11:1441372
|
G | GCCCCCCA others(153): Show |
1 | a0002c0002t0002g0014 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.413+521_413+522ins others(160): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441372 | |||||
| chr11:1441372
|
G | GCCCCCCA others(285): Show |
2 | a0001c0001t0063g0253a0002c0002t0005g0198 | 2 | HG00639.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.413+734_414-537dup others(292): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441372 | |||||
| chr11:1441372
|
GCCCCCCA others(285): Show |
G | 22 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0062others(19): Show | 22 | HG00438.hp2 HG01123.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.413+734_414-537del | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441372 | |||||
| chr11:1441473
|
CCCCCATT others(25): Show |
C | 1 | a0001c0001t0074g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.413+609_413+640del others(32): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441473 | |||||
| chr11:1441479
|
T | A | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+551T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441479 | ||||||
| chr11:1441484
|
T | G | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+556T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441484 | ||||||
| chr11:1441485
|
A | G | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+557A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441485 | ||||||
| chr11:1441501
|
G | A | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+573G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441501 | ||||||
| chr11:1441501
|
G | GTCCCCCC others(217): Show |
1 | a0002c0002t0002g0320 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.413+576_413+577ins others(224): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441501 | |||||
| chr11:1441505
|
A | ACCCCATT others(221): Show |
1 | a0001c0001t0024g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.413+608_413+609ins others(228): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441505 | |||||
| chr11:1441505
|
A | C | 2 | a0001c0001t0004g0081a0002c0002t0002g0320 | 2 | HG02080.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.413+577A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441505 | ||||||
| chr11:1441514
|
G | A | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+586G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441514 | ||||||
| chr11:1441537
|
A | C | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+609A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441537 | ||||||
| chr11:1441548
|
T | G | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+620T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441548 | ||||||
| chr11:1441549
|
A | G | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+621A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441549 | ||||||
| chr11:1441565
|
G | C | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+637G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441565 | ||||||
| chr11:1441580
|
A | G | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+652A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441580 | ||||||
| chr11:1441596
|
A | G | 1 | a0002c0002t0002g0320 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.413+668A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441596 | ||||||
| chr11:1441603
|
T | C | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+675T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441603 | ||||||
| chr11:1441609
|
G | A | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+681G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441609 | ||||||
| chr11:1441620
|
G | A | 2 | a0001c0001t0004g0081a0002c0002t0002g0320 | 2 | HG02080.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.413+692G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441620 | ||||||
| chr11:1441626
|
T | C | 2 | a0001c0001t0004g0081a0002c0002t0002g0320 | 2 | HG02080.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.413+698T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441626 | ||||||
| chr11:1441632
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.413+704C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441632 | ||||||
| chr11:1441637
|
T | C | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+709T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441637 | ||||||
| chr11:1441645
|
T | G | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+717T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441645 | ||||||
| chr11:1441646
|
G | A | 1 | a0002c0002t0002g0320 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.413+718G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441646 | ||||||
| chr11:1441654
|
A | G | 1 | a0002c0002t0002g0320 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.413+726A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441654 | ||||||
| chr11:1441660
|
C | T | 1 | a0002c0002t0002g0320 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.413+732C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441660 | ||||||
| chr11:1441662
|
A | G | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+734A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441662 | ||||||
| chr11:1441664
|
C | G | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.413+736C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441664 | ||||||
| chr11:1441669
|
C | T | 1 | a0002c0002t0002g0320 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.413+741C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441669 | ||||||
| chr11:1441765
|
C | CCCCCATT others(57): Show |
1 | a0002c0002t0005g0211 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.414-693_414-630dup others(64): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441765 | |||||
| chr11:1441765
|
CCCCCATT others(25): Show |
C | 9 | a0001c0001t0001g0010a0001c0001t0001g0343a0001c0001t0004g0175others(6): Show | 9 | HG01069.hp1 HG01993.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-661_414-630del others(32): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441765 | |||||
| chr11:1441792
|
C | T | 1 | a0002c0002t0002g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.414-698C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441792 | ||||||
| chr11:1441797
|
ACCCCATT others(56): Show |
A | 3 | a0001c0001t0014g0039a0001c0001t0044g0016a0001c0001t0045g0040 | 3 | HG01192.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.414-665_414-603del others(63): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441797 | |||||
| chr11:1441825
|
G | A | 1 | a0001c0001t0047g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-665G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441825 | ||||||
| chr11:1441829
|
A | C | 1 | a0001c0001t0047g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-661A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441829 | ||||||
| chr11:1441832
|
C | T | 1 | a0001c0001t0047g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-658C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441832 | ||||||
| chr11:1441841
|
A | ACCCCTCA others(90): Show |
1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.414-625_414-529dup others(97): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441841 | |||||
| chr11:1441844
|
C | CCTCAAGT others(285): Show |
3 | a0001c0001t0001g0048a0001c0001t0043g0050a0002c0002t0002g0015 | 3 | HG02647.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.414-537_414-536ins others(292): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441844 | |||||
| chr11:1441844
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.414-646C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441844 | ||||||
| chr11:1441849
|
A | G | 1 | a0001c0001t0047g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-641A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441849 | ||||||
| chr11:1441855
|
C | T | 1 | a0001c0001t0047g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-635C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441855 | ||||||
| chr11:1441857
|
G | A | 2 | a0001c0001t0047g0340a0002c0002t0013g0001 | 3 | HG01243.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.414-633G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441857 | ||||||
| chr11:1441860
|
C | CCCCCATT others(286): Show |
1 | a0002c0002t0016g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.414-537_414-536ins others(293): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441860 | |||||
| chr11:1441863
|
C | T | 1 | a0001c0001t0047g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-627C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441863 | ||||||
| chr11:1441872
|
A | G | 1 | a0001c0001t0047g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-618A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441872 | ||||||
| chr11:1441875
|
C | T | 1 | a0003c0014t0002g0319 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.414-615C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441875 | ||||||
| chr11:1441888
|
A | G | 1 | a0001c0001t0047g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-602A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441888 | ||||||
| chr11:1441895
|
T | C | 1 | a0001c0001t0047g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-595T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441895 | ||||||
| chr11:1441929
|
TCATTAGC others(25): Show |
T | 1 | a0001c0001t0047g0340 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-552_414-521del others(32): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441929 | |||||
| chr11:1441938
|
G | GCCCCTCA others(124): Show |
1 | a0002c0002t0033g0279 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.414-537_414-536ins others(131): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441938 | |||||
| chr11:1441942
|
C | G | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.414-548C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441942 | ||||||
| chr11:1441961
|
C | CCATTAGC others(27): Show |
4 | a0001c0001t0031g0012a0001c0001t0032g0195a0001c0001t0032g0209others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-513_414-512ins others(34): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 1441961 | |||||
| chr11:1441970
|
A | G | 26 | a0001c0001t0001g0154a0001c0001t0001g0189a0001c0001t0001g0191others(23): Show | 26 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.414-520A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1441970 | ||||||
| chr11:1442231
|
G | A | 1 | a0002c0002t0002g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.414-259G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1442231 | ||||||
| chr11:1442242
|
G | A | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.414-248G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1442242 | ||||||
| chr11:1442322
|
G | A | 1 | a0001c0003t0014g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.414-168G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1442322 | ||||||
| chr11:1442324
|
C | T | 1 | a0002c0002t0058g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.414-166C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1442324 | ||||||
| chr11:1442356
|
G | A | 1 | a0001c0001t0004g0090 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.414-134G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 4/19 | chr11 | 1442356 | ||||||
| chr11:1442683
|
C | G | 1 | a0001c0003t0001g0070 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.530+77C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 5/19 | chr11 | 1442683 | ||||||
| chr11:1442817
|
T | G | 25 | a0001c0001t0001g0154a0001c0001t0001g0189a0001c0001t0001g0191others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.530+211T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 5/19 | chr11 | 1442817 | ||||||
| chr11:1442864
|
C | A | 1 | a0002c0007t0010g0244 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.531-242C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 5/19 | chr11 | 1442864 | ||||||
| chr11:1442872
|
G | T | 2 | a0002c0002t0015g0028a0002c0002t0015g0330 | 2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.531-234G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 5/19 | chr11 | 1442872 | ||||||
| chr11:1442875
|
A | AC | 9 | a0001c0001t0004g0080a0001c0001t0021g0221a0001c0001t0067g0252others(6): Show | 9 | HG00642.hp1 HG00741.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.531-226dupC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr11 | 1442875 | |||||
| chr11:1442901
|
G | A | 31 | a0001c0001t0001g0049a0001c0001t0001g0087a0001c0001t0001g0107others(28): Show | 32 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.531-205G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 5/19 | chr11 | 1442901 | ||||||
| chr11:1442963
|
C | T | 1 | a0002c0002t0005g0211 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.531-143C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 5/19 | chr11 | 1442963 | ||||||
| chr11:1442973
|
T | C | 1 | a0001c0001t0004g0080 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.531-133T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 5/19 | chr11 | 1442973 | ||||||
| chr11:1443032
|
G | A | 1 | a0002c0002t0015g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.531-74G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 5/19 | chr11 | 1443032 | ||||||
| chr11:1443067
|
G | A | 1 | a0002c0002t0005g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.531-39G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 5/19 | chr11 | 1443067 | ||||||
| chr11:1443152
|
C | T | 14 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0312others(11): Show | 14 | HG00642.hp1 HG01070.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.564+13C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 6/19 | chr11 | 1443152 | ||||||
| chr11:1443155
|
C | T | 1 | a0002c0002t0007g0345 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.564+16C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 6/19 | chr11 | 1443155 | ||||||
| chr11:1443158
|
G | A | 4 | a0001c0003t0003g0291a0002c0005t0005g0289a0002c0005t0034g0055others(1): Show | 4 | HG01346.hp2 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+19G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 6/19 | chr11 | 1443158 | ||||||
| chr11:1443222
|
C | A | 1 | a0001c0001t0001g0059 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.564+83C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 6/19 | chr11 | 1443222 | ||||||
| chr11:1443639
|
C | T | 1 | a0002c0002t0016g0284 | 1 | HG04115.hp1 | splice_region_variant&intron_variant | LOW | c.780+4C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443639 | ||||||
| chr11:1443652
|
C | G | 4 | a0001c0003t0003g0291a0002c0005t0005g0289a0002c0005t0034g0055others(1): Show | 4 | HG01346.hp2 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+17C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443652 | ||||||
| chr11:1443653
|
G | A | 7 | a0001c0003t0001g0115a0001c0003t0001g0146a0001c0003t0003g0291others(4): Show | 7 | HG01346.hp2 HG02717.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+18G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443653 | ||||||
| chr11:1443673
|
CG | C | 239 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0017others(236): Show | 242 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.780+45delG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 1443673 | |||||
| chr11:1443679
|
G | GC | 3 | a0001c0001t0001g0110a0001c0001t0001g0317a0001c0001t0018g0137 | 3 | HG00544.hp1 HG01261.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.780+44_780+45insC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443679 | ||||||
| chr11:1443682
|
G | A | 1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.780+47G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443682 | ||||||
| chr11:1443682
|
GC | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0317a0001c0001t0018g0137 | 3 | HG00544.hp1 HG01261.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.780+48delC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443682 | ||||||
| chr11:1443701
|
TGTGTGTG others(5): Show |
T | 6 | a0001c0001t0001g0141a0002c0002t0008g0116a0002c0002t0010g0246others(3): Show | 6 | HG01099.hp1 HG01167.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+75_780+86delAC others(10): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 1443701 | |||||
| chr11:1443772
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.780+137G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443772 | ||||||
| chr11:1443919
|
T | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+284T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443919 | ||||||
| chr11:1443920
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+285G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443920 | ||||||
| chr11:1443921
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+286G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443921 | ||||||
| chr11:1443922
|
G | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+287G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443922 | ||||||
| chr11:1443923
|
T | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+288T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443923 | ||||||
| chr11:1443924
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+289G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443924 | ||||||
| chr11:1443925
|
C | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+290C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1443925 | ||||||
| chr11:1444017
|
T | G | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+382T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444017 | ||||||
| chr11:1444031
|
C | T | 10 | a0001c0001t0004g0161a0001c0001t0004g0175a0001c0001t0004g0177others(7): Show | 10 | HG00639.hp2 HG01069.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.780+396C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444031 | ||||||
| chr11:1444081
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+446G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444081 | ||||||
| chr11:1444082
|
T | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+447T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444082 | ||||||
| chr11:1444083
|
G | T | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+448G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444083 | ||||||
| chr11:1444085
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+450G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444085 | ||||||
| chr11:1444091
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+456G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444091 | ||||||
| chr11:1444092
|
T | G | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+457T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444092 | ||||||
| chr11:1444093
|
G | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+458G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444093 | ||||||
| chr11:1444094
|
T | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+459T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444094 | ||||||
| chr11:1444095
|
G | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+460G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444095 | ||||||
| chr11:1444096
|
G | T | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+461G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444096 | ||||||
| chr11:1444099
|
G | T | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.780+464G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444099 | ||||||
| chr11:1444130
|
A | G | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.780+495A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444130 | ||||||
| chr11:1444210
|
G | A | 1 | a0002c0008t0005g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.780+575G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444210 | ||||||
| chr11:1444304
|
C | G | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-667C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444304 | ||||||
| chr11:1444306
|
T | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-665T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444306 | ||||||
| chr11:1444307
|
G | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-664G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444307 | ||||||
| chr11:1444308
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-663G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444308 | ||||||
| chr11:1444309
|
T | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-662T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444309 | ||||||
| chr11:1444310
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-661G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444310 | ||||||
| chr11:1444311
|
T | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-660T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444311 | ||||||
| chr11:1444312
|
G | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-659G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444312 | ||||||
| chr11:1444313
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-658G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444313 | ||||||
| chr11:1444315
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-656G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444315 | ||||||
| chr11:1444324
|
T | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-647T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444324 | ||||||
| chr11:1444331
|
T | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-640T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444331 | ||||||
| chr11:1444333
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-638G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444333 | ||||||
| chr11:1444334
|
A | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-637A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444334 | ||||||
| chr11:1444344
|
G | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-627G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444344 | ||||||
| chr11:1444345
|
T | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-626T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444345 | ||||||
| chr11:1444347
|
A | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-624A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444347 | ||||||
| chr11:1444351
|
T | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-620T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444351 | ||||||
| chr11:1444353
|
T | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-618T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444353 | ||||||
| chr11:1444355
|
G | GCAACCCA others(3): Show |
1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-616_781-615ins others(10): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444355 | ||||||
| chr11:1444365
|
T | G | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-606T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444365 | ||||||
| chr11:1444370
|
G | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-601G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444370 | ||||||
| chr11:1444371
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-600G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444371 | ||||||
| chr11:1444372
|
T | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-599T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444372 | ||||||
| chr11:1444379
|
G | C | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.781-592G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444379 | ||||||
| chr11:1444393
|
T | C | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-578T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444393 | ||||||
| chr11:1444394
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781-577G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444394 | ||||||
| chr11:1444529
|
T | C | 351 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(348): Show | 357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.781-442T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444529 | ||||||
| chr11:1444568
|
G | T | 2 | a0001c0001t0032g0209a0001c0001t0070g0210 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.781-403G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444568 | ||||||
| chr11:1444636
|
G | C | 1 | a0001c0001t0075g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.781-335G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444636 | ||||||
| chr11:1444658
|
C | T | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.781-313C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444658 | ||||||
| chr11:1444824
|
T | C | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.781-147T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 8/19 | chr11 | 1444824 | ||||||
| chr11:1445082
|
A | G | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.812+80A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 9/19 | chr11 | 1445082 | ||||||
| chr11:1445125
|
G | C | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.812+123G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 9/19 | chr11 | 1445125 | ||||||
| chr11:1445226
|
G | C | 29 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(26): Show | 29 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.813-68G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 9/19 | chr11 | 1445226 | ||||||
| chr11:1445253
|
G | A | 4 | a0001c0003t0003g0291a0002c0005t0005g0289a0002c0005t0034g0055others(1): Show | 4 | HG01346.hp2 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.813-41G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 9/19 | chr11 | 1445253 | ||||||
| chr11:1445490
|
G | A | 31 | a0001c0001t0001g0049a0001c0001t0001g0087a0001c0001t0001g0107others(28): Show | 32 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.977+32G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 10/19 | chr11 | 1445490 | ||||||
| chr11:1445515
|
C | T | 1 | a0002c0002t0033g0279 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.978-56C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 10/19 | chr11 | 1445515 | ||||||
| chr11:1445545
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0097 | 2 | NA19005.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.978-26C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 10/19 | chr11 | 1445545 | ||||||
| chr11:1445551
|
G | A | 1 | a0001c0001t0003g0265 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.978-20G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 10/19 | chr11 | 1445551 | ||||||
| chr11:1445563
|
C | T | 1 | a0002c0002t0015g0327 | 1 | HG04199.hp2 | splice_region_variant&intron_variant | LOW | c.978-8C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 10/19 | chr11 | 1445563 | ||||||
| chr11:1445696
|
C | T | 2 | a0001c0001t0004g0188a0001c0015t0001g0315 | 2 | HG01433.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1075+28C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 11/19 | chr11 | 1445696 | ||||||
| chr11:1445714
|
C | T | 4 | a0001c0003t0014g0036a0001c0003t0014g0037a0001c0003t0014g0038others(1): Show | 4 | HG00642.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076-43C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 11/19 | chr11 | 1445714 | ||||||
| chr11:1445722
|
G | A | 23 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0134others(20): Show | 23 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1076-35G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 11/19 | chr11 | 1445722 | ||||||
| chr11:1445732
|
T | C | 3 | a0001c0001t0001g0057a0001c0001t0001g0111a0001c0001t0003g0280 | 3 | HG04184.hp2 NA18950.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1076-25T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 11/19 | chr11 | 1445732 | ||||||
| chr11:1445956
|
C | T | 2 | a0002c0007t0010g0244a0002c0007t0010g0245 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1226+49C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1445956 | ||||||
| chr11:1446046
|
AGCTGGGC others(8): Show |
A | 82 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(79): Show | 84 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1226+148_1226+162d others(17): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 1446046 | |||||
| chr11:1446050
|
G | GGGCTGGG others(13): Show |
1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1226+164_1226+183d others(22): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 1446050 | |||||
| chr11:1446051
|
G | GGCTTGGC others(28): Show |
1 | a0002c0002t0049g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1226+147_1226+148i others(37): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 1446051 | |||||
| chr11:1446055
|
G | T | 4 | a0001c0001t0001g0141a0002c0002t0008g0116a0002c0002t0010g0246others(1): Show | 4 | HG01099.hp1 HG01167.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1226+148G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446055 | ||||||
| chr11:1446061
|
G | GGCTGGGC others(8): Show |
4 | a0001c0001t0001g0141a0002c0002t0008g0116a0002c0002t0010g0246others(1): Show | 4 | HG01099.hp1 HG01167.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1226+162_1226+163i others(17): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 1446061 | |||||
| chr11:1446066
|
G | GGA | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1226+160_1226+161i others(4): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 1446066 | |||||
| chr11:1446070
|
T | G | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1226+163T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446070 | ||||||
| chr11:1446071
|
G | A | 27 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1226+164G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446071 | ||||||
| chr11:1446071
|
G | T | 4 | a0001c0001t0001g0141a0002c0002t0008g0116a0002c0002t0010g0246others(1): Show | 4 | HG01099.hp1 HG01167.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1226+164G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446071 | ||||||
| chr11:1446076
|
GGCTGGGC others(1): Show |
G | 4 | a0001c0003t0003g0291a0002c0005t0005g0289a0002c0005t0034g0055others(1): Show | 4 | HG01346.hp2 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1226+171_1226+178d others(10): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 1446076 | |||||
| chr11:1446086
|
G | A | 4 | a0001c0003t0003g0291a0002c0005t0005g0289a0002c0005t0034g0055others(1): Show | 4 | HG01346.hp2 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1226+179G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446086 | ||||||
| chr11:1446090
|
T | A | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1226+183T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446090 | ||||||
| chr11:1446090
|
T | G | 4 | a0001c0003t0003g0291a0002c0005t0005g0289a0002c0005t0034g0055others(1): Show | 4 | HG01346.hp2 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1226+183T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446090 | ||||||
| chr11:1446096
|
G | A | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1226+189G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446096 | ||||||
| chr11:1446096
|
GGCTGGGC others(15): Show |
G | 1 | a0001c0001t0011g0352 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1226+204_1226+225d others(24): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 1446096 | |||||
| chr11:1446106
|
G | T | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1226+199G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446106 | ||||||
| chr11:1446109
|
TGG | T | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1226+204_1226+205d others(4): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 1446109 | |||||
| chr11:1446112
|
G | A | 4 | a0001c0003t0003g0291a0002c0005t0005g0289a0002c0005t0034g0055others(1): Show | 4 | HG01346.hp2 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1226+205G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446112 | ||||||
| chr11:1446113
|
A | T | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1226+206A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446113 | ||||||
| chr11:1446118
|
A | G | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1226+211A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446118 | ||||||
| chr11:1446119
|
G | A | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1226+212G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446119 | ||||||
| chr11:1446123
|
G | GACTGGGC others(52): Show |
1 | a0001c0004t0001g0094 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1226+216_1226+217i others(61): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446123 | ||||||
| chr11:1446123
|
G | GACTGGGC others(53): Show |
25 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(22): Show | 25 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1226+216_1226+217i others(62): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446123 | ||||||
| chr11:1446128
|
G | T | 4 | a0001c0003t0003g0291a0002c0005t0005g0289a0002c0005t0034g0055others(1): Show | 4 | HG01346.hp2 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1226+221G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446128 | ||||||
| chr11:1446133
|
T | G | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1226+226T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446133 | ||||||
| chr11:1446139
|
A | T | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1226+232A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446139 | ||||||
| chr11:1446142
|
G | A | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1226+235G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446142 | ||||||
| chr11:1446147
|
G | A | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1226+240G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446147 | ||||||
| chr11:1446149
|
G | A | 26 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1226+242G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446149 | ||||||
| chr11:1446149
|
G | GCTAGGCT others(73): Show |
4 | a0001c0003t0003g0291a0002c0005t0005g0289a0002c0005t0034g0055others(1): Show | 4 | HG01346.hp2 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1226+249_1226+250i others(82): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 1446149 | |||||
| chr11:1446173
|
G | A | 34 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0099others(31): Show | 34 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1226+266G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446173 | ||||||
| chr11:1446187
|
A | G | 67 | a0001c0001t0001g0049a0001c0001t0001g0063a0001c0001t0001g0069others(64): Show | 68 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1226+280A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446187 | ||||||
| chr11:1446195
|
C | G | 11 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0099others(8): Show | 11 | HG00423.hp1 NA18939.hp2 NA18940.hp1 others(8): Show |
intron_variant | MODIFIER | c.1226+288C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446195 | ||||||
| chr11:1446245
|
C | T | 1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1226+338C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446245 | ||||||
| chr11:1446253
|
C | G | 1 | a0002c0002t0005g0283 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1226+346C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446253 | ||||||
| chr11:1446279
|
G | A | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1226+372G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446279 | ||||||
| chr11:1446342
|
ACTGGGCT others(13): Show |
A | 1 | a0002c0002t0007g0304 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1226+464_1226+483d others(22): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 1446342 | |||||
| chr11:1446351
|
AGCTGGGC others(28): Show |
A | 1 | a0001c0001t0003g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1226+452_1226+486d others(37): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 1446351 | |||||
| chr11:1446359
|
A | AGGGCTGG others(3): Show |
1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1226+454_1226+463d others(12): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 1446359 | |||||
| chr11:1446379
|
A | AGGGCT | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1226+483_1226+487d others(7): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 1446379 | |||||
| chr11:1446622
|
C | T | 33 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0087others(30): Show | 34 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1226+715C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446622 | ||||||
| chr11:1446725
|
G | A | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1226+818G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446725 | ||||||
| chr11:1446827
|
G | A | 1 | a0002c0005t0005g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1226+920G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446827 | ||||||
| chr11:1446900
|
G | C | 29 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(26): Show | 29 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1226+993G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446900 | ||||||
| chr11:1446901
|
G | A | 1 | a0001c0003t0001g0135 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1226+994G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446901 | ||||||
| chr11:1446901
|
G | C | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1226+994G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446901 | ||||||
| chr11:1446932
|
G | C | 2 | a0001c0001t0018g0334a0001c0001t0067g0252 | 2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1226+1025G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446932 | ||||||
| chr11:1446948
|
G | C | 3 | a0001c0001t0003g0194a0001c0001t0003g0196a0001c0001t0003g0237 | 3 | HG02559.hp1 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1226+1041G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1446948 | ||||||
| chr11:1447013
|
G | T | 3 | a0002c0002t0022g0003a0002c0002t0022g0204a0002c0002t0073g0217 | 4 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1226+1106G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1447013 | ||||||
| chr11:1447124
|
C | G | 1 | a0001c0001t0024g0299 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1226+1217C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1447124 | ||||||
| chr11:1447163
|
C | T | 1 | a0002c0002t0005g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1226+1256C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1447163 | ||||||
| chr11:1447164
|
G | C | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1226+1257G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1447164 | ||||||
| chr11:1447248
|
A | T | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1226+1341A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1447248 | ||||||
| chr11:1447448
|
C | T | 1 | a0002c0002t0015g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1226+1541C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1447448 | ||||||
| chr11:1447509
|
C | T | 2 | a0001c0001t0001g0067a0001c0001t0004g0084 | 2 | NA18947.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1226+1602C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1447509 | ||||||
| chr11:1447651
|
C | T | 1 | a0002c0002t0008g0167 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1226+1744C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1447651 | ||||||
| chr11:1447909
|
C | T | 1 | a0001c0001t0018g0334 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1227-1867C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1447909 | ||||||
| chr11:1448016
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0003g0002others(1): Show | 5 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1227-1760C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448016 | ||||||
| chr11:1448041
|
G | A | 1 | a0002c0002t0015g0027 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1227-1735G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448041 | ||||||
| chr11:1448045
|
G | T | 1 | a0001c0015t0001g0315 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1227-1731G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448045 | ||||||
| chr11:1448119
|
C | T | 2 | a0002c0005t0034g0055a0002c0005t0034g0056 | 2 | HG01346.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1227-1657C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448119 | ||||||
| chr11:1448148
|
C | T | 1 | a0001c0001t0077g0324 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1227-1628C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448148 | ||||||
| chr11:1448228
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1227-1548C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448228 | ||||||
| chr11:1448271
|
C | T | 1 | a0001c0001t0044g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1227-1505C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448271 | ||||||
| chr11:1448319
|
G | T | 2 | a0002c0005t0034g0055a0002c0005t0034g0056 | 2 | HG01346.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1227-1457G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448319 | ||||||
| chr11:1448325
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1227-1451C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448325 | ||||||
| chr11:1448326
|
G | C | 29 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0134others(26): Show | 29 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1227-1450G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448326 | ||||||
| chr11:1448518
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1227-1258G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448518 | ||||||
| chr11:1448601
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1227-1175G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448601 | ||||||
| chr11:1448825
|
C | G | 4 | a0002c0002t0005g0211a0002c0002t0007g0302a0002c0002t0007g0306others(1): Show | 4 | NA18990.hp2 NA18993.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227-951C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448825 | ||||||
| chr11:1448926
|
G | T | 6 | a0001c0001t0001g0066a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 6 | HG01123.hp1 HG01256.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1227-850G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448926 | ||||||
| chr11:1448945
|
T | C | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.1227-831T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1448945 | ||||||
| chr11:1449094
|
C | T | 13 | a0001c0001t0001g0087a0001c0001t0001g0107a0001c0001t0001g0339others(10): Show | 14 | HG00280.hp1 HG00609.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1227-682C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449094 | ||||||
| chr11:1449116
|
C | T | 3 | a0001c0001t0006g0197a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG00735.hp1 HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1227-660C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449116 | ||||||
| chr11:1449125
|
C | T | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1227-651C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449125 | ||||||
| chr11:1449216
|
A | T | 30 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1227-560A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449216 | ||||||
| chr11:1449227
|
C | T | 1 | a0002c0002t0020g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1227-549C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449227 | ||||||
| chr11:1449237
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1227-539C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449237 | ||||||
| chr11:1449296
|
C | T | 5 | a0002c0002t0010g0246a0002c0002t0015g0027a0002c0002t0016g0284others(2): Show | 5 | HG01167.hp2 HG01891.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1227-480C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449296 | ||||||
| chr11:1449306
|
C | G | 2 | a0001c0001t0001g0343a0001c0001t0047g0340 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1227-470C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449306 | ||||||
| chr11:1449361
|
T | A | 2 | a0002c0002t0015g0028a0002c0002t0015g0330 | 2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1227-415T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449361 | ||||||
| chr11:1449380
|
G | C | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1227-396G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449380 | ||||||
| chr11:1449417
|
T | C | 7 | a0001c0001t0075g0202a0001c0003t0003g0291a0002c0002t0015g0028others(4): Show | 7 | HG01346.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1227-359T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449417 | ||||||
| chr11:1449461
|
C | T | 28 | a0001c0003t0001g0070a0001c0003t0001g0114a0001c0003t0001g0115others(25): Show | 28 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1227-315C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449461 | ||||||
| chr11:1449464
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1227-312C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449464 | ||||||
| chr11:1449470
|
G | A | 1 | a0001c0001t0004g0316 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1227-306G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449470 | ||||||
| chr11:1449499
|
C | T | 1 | a0001c0001t0003g0265 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1227-277C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449499 | ||||||
| chr11:1449608
|
C | T | 1 | a0001c0001t0003g0193 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1227-168C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449608 | ||||||
| chr11:1449738
|
C | G | 2 | a0001c0006t0001g0047a0001c0006t0027g0142 | 2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1227-38C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449738 | ||||||
| chr11:1449757
|
T | C | 1 | a0002c0002t0002g0320 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1227-19T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 12/19 | chr11 | 1449757 | ||||||
| chr11:1449865
|
C | T | 1 | a0001c0001t0003g0227 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1287+29C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1449865 | ||||||
| chr11:1449924
|
C | T | 224 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0029others(221): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1287+88C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1449924 | ||||||
| chr11:1449963
|
C | T | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1287+127C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1449963 | ||||||
| chr11:1449991
|
C | T | 84 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0046others(81): Show | 84 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1287+155C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1449991 | ||||||
| chr11:1450056
|
C | G | 164 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0052others(161): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1287+220C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450056 | ||||||
| chr11:1450103
|
A | C | 1 | a0002c0002t0038g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1287+267A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450103 | ||||||
| chr11:1450106
|
C | G | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1287+270C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450106 | ||||||
| chr11:1450216
|
C | T | 2 | a0001c0003t0001g0138a0001c0003t0026g0354 | 2 | HG00558.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1288-371C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450216 | ||||||
| chr11:1450334
|
CGTCCTCC others(4): Show |
C | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-251_1288-241d others(13): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr11 | 1450334 | |||||
| chr11:1450347
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-240C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450347 | ||||||
| chr11:1450349
|
G | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-238G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450349 | ||||||
| chr11:1450350
|
G | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-237G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450350 | ||||||
| chr11:1450352
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-235C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450352 | ||||||
| chr11:1450354
|
C | T | 1 | a0001c0015t0001g0315 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1288-233C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450354 | ||||||
| chr11:1450355
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-232C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450355 | ||||||
| chr11:1450359
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-228C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450359 | ||||||
| chr11:1450364
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-223C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450364 | ||||||
| chr11:1450365
|
G | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-222G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450365 | ||||||
| chr11:1450367
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-220C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450367 | ||||||
| chr11:1450368
|
C | G | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-219C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450368 | ||||||
| chr11:1450369
|
C | G | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-218C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450369 | ||||||
| chr11:1450370
|
C | G | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-217C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450370 | ||||||
| chr11:1450372
|
A | G | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-215A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450372 | ||||||
| chr11:1450374
|
A | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-213A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450374 | ||||||
| chr11:1450375
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-212C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450375 | ||||||
| chr11:1450376
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-211C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450376 | ||||||
| chr11:1450379
|
G | C | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-208G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450379 | ||||||
| chr11:1450380
|
A | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-207A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450380 | ||||||
| chr11:1450382
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-205C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450382 | ||||||
| chr11:1450386
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-201C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450386 | ||||||
| chr11:1450387
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-200C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450387 | ||||||
| chr11:1450388
|
G | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-199G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450388 | ||||||
| chr11:1450394
|
G | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-193G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450394 | ||||||
| chr11:1450397
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-190C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450397 | ||||||
| chr11:1450398
|
A | C | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-189A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450398 | ||||||
| chr11:1450400
|
G | C | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-187G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450400 | ||||||
| chr11:1450401
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-186C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450401 | ||||||
| chr11:1450403
|
G | C | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-184G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450403 | ||||||
| chr11:1450406
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-181C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450406 | ||||||
| chr11:1450407
|
G | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-180G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450407 | ||||||
| chr11:1450409
|
C | G | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-178C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450409 | ||||||
| chr11:1450410
|
A | G | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-177A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450410 | ||||||
| chr11:1450413
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-174C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450413 | ||||||
| chr11:1450414
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-173C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450414 | ||||||
| chr11:1450419
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-168C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450419 | ||||||
| chr11:1450430
|
G | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-157G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450430 | ||||||
| chr11:1450436
|
C | T | 2 | a0001c0001t0013g0311a0002c0002t0017g0353 | 2 | HG02630.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1288-151C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450436 | ||||||
| chr11:1450438
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-149C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450438 | ||||||
| chr11:1450439
|
C | G | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-148C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450439 | ||||||
| chr11:1450442
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-145C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450442 | ||||||
| chr11:1450444
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-143C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450444 | ||||||
| chr11:1450445
|
G | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-142G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450445 | ||||||
| chr11:1450449
|
A | C | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-138A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450449 | ||||||
| chr11:1450451
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-136C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450451 | ||||||
| chr11:1450452
|
A | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-135A>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450452 | ||||||
| chr11:1450453
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-134C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450453 | ||||||
| chr11:1450456
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-131C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450456 | ||||||
| chr11:1450458
|
G | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-129G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450458 | ||||||
| chr11:1450459
|
C | G | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-128C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450459 | ||||||
| chr11:1450460
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-127C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450460 | ||||||
| chr11:1450461
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-126C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450461 | ||||||
| chr11:1450461
|
C | T | 3 | a0001c0001t0042g0160a0001c0001t0060g0163a0002c0002t0002g0014 | 3 | HG02723.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1288-126C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450461 | ||||||
| chr11:1450471
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-116C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450471 | ||||||
| chr11:1450472
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-115C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450472 | ||||||
| chr11:1450474
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-113C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450474 | ||||||
| chr11:1450475
|
T | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-112T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450475 | ||||||
| chr11:1450478
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-109C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450478 | ||||||
| chr11:1450480
|
T | C | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-107T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450480 | ||||||
| chr11:1450481
|
T | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-106T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450481 | ||||||
| chr11:1450482
|
T | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-105T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450482 | ||||||
| chr11:1450483
|
G | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-104G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450483 | ||||||
| chr11:1450485
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-102C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450485 | ||||||
| chr11:1450486
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-101C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450486 | ||||||
| chr11:1450493
|
G | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-94G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450493 | ||||||
| chr11:1450495
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1288-92C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450495 | ||||||
| chr11:1450498
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-89C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450498 | ||||||
| chr11:1450501
|
C | T | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-86C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450501 | ||||||
| chr11:1450502
|
C | A | 1 | a0002c0002t0017g0353 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1288-85C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450502 | ||||||
| chr11:1450521
|
C | T | 92 | a0001c0001t0001g0059a0001c0001t0001g0063a0001c0001t0001g0066others(89): Show | 94 | HG00280.hp1 HG00544.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1288-66C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450521 | ||||||
| chr11:1450522
|
G | T | 1 | a0001c0004t0001g0094 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1288-65G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450522 | ||||||
| chr11:1450528
|
C | T | 44 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0049others(41): Show | 46 | HG01109.hp2 HG01243.hp1 HG01346.hp2 others(43): Show |
intron_variant | MODIFIER | c.1288-59C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450528 | ||||||
| chr11:1450530
|
C | G | 1 | a0001c0001t0003g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1288-57C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450530 | ||||||
| chr11:1450539
|
C | T | 21 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0312others(18): Show | 21 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1288-48C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450539 | ||||||
| chr11:1450575
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1288-12C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 13/19 | chr11 | 1450575 | ||||||
| chr11:1450820
|
A | G | 44 | a0001c0001t0001g0113a0001c0001t0003g0219a0001c0001t0003g0220others(41): Show | 44 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1495+26A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 14/19 | chr11 | 1450820 | ||||||
| chr11:1450863
|
G | A | 1 | a0001c0001t0006g0248 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1495+69G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 14/19 | chr11 | 1450863 | ||||||
| chr11:1450903
|
A | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 6 | HG01943.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495+109A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 14/19 | chr11 | 1450903 | ||||||
| chr11:1450939
|
G | A | 2 | a0001c0001t0001g0062a0002c0002t0058g0325 | 2 | HG02280.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1495+145G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 14/19 | chr11 | 1450939 | ||||||
| chr11:1450974
|
G | A | 24 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0004g0136others(21): Show | 24 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1495+180G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 14/19 | chr11 | 1450974 | ||||||
| chr11:1451094
|
C | G | 1 | a0001c0001t0045g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1496-277C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 14/19 | chr11 | 1451094 | ||||||
| chr11:1451102
|
G | A | 2 | a0001c0001t0004g0175a0001c0001t0004g0180 | 2 | HG01993.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1496-269G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 14/19 | chr11 | 1451102 | ||||||
| chr11:1451189
|
G | T | 1 | a0002c0002t0002g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1496-182G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 14/19 | chr11 | 1451189 | ||||||
| chr11:1451220
|
G | A | 1 | a0002c0002t0016g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1496-151G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 14/19 | chr11 | 1451220 | ||||||
| chr11:1451245
|
TG | T | 242 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(239): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1496-119delG | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr11 | 1451245 | |||||
| chr11:1451279
|
C | T | 2 | a0001c0001t0001g0328a0001c0001t0001g0329 | 2 | HG03017.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1496-92C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 14/19 | chr11 | 1451279 | ||||||
| chr11:1451299
|
G | A | 12 | a0001c0001t0001g0130a0001c0001t0001g0141a0002c0002t0002g0118others(9): Show | 13 | HG00609.hp2 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1496-72G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 14/19 | chr11 | 1451299 | ||||||
| chr11:1451443
|
T | G | 2 | a0001c0001t0018g0334a0001c0001t0067g0252 | 2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1544+24T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1451443 | ||||||
| chr11:1451553
|
G | A | 1 | a0001c0001t0044g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1544+134G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1451553 | ||||||
| chr11:1451587
|
C | T | 1 | a0002c0002t0005g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1544+168C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1451587 | ||||||
| chr11:1451659
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0011g0295 | 2 | NA18952.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1544+240C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1451659 | ||||||
| chr11:1451822
|
A | G | 54 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0053others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1544+403A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1451822 | ||||||
| chr11:1451898
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1544+479C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1451898 | ||||||
| chr11:1451927
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1544+508G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1451927 | ||||||
| chr11:1451950
|
G | T | 1 | a0001c0003t0001g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1544+531G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1451950 | ||||||
| chr11:1451977
|
C | T | 1 | a0002c0002t0002g0176 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1544+558C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1451977 | ||||||
| chr11:1451978
|
G | A | 44 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(41): Show | 44 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.1544+559G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1451978 | ||||||
| chr11:1452049
|
C | T | 2 | a0001c0001t0018g0334a0001c0001t0067g0252 | 2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1544+630C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452049 | ||||||
| chr11:1452187
|
C | T | 47 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(44): Show | 47 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.1544+768C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452187 | ||||||
| chr11:1452191
|
C | T | 1 | a0001c0001t0044g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1544+772C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452191 | ||||||
| chr11:1452233
|
A | G | 2 | a0002c0002t0015g0028a0002c0002t0015g0330 | 2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1544+814A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452233 | ||||||
| chr11:1452282
|
C | T | 2 | a0001c0001t0018g0334a0001c0001t0067g0252 | 2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1544+863C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452282 | ||||||
| chr11:1452312
|
C | T | 1 | a0002c0002t0002g0158 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1544+893C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452312 | ||||||
| chr11:1452377
|
A | G | 1 | a0002c0002t0008g0151 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1544+958A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452377 | ||||||
| chr11:1452475
|
G | T | 1 | a0001c0001t0003g0200 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1544+1056G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452475 | ||||||
| chr11:1452493
|
C | T | 1 | a0002c0002t0017g0305 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1544+1074C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452493 | ||||||
| chr11:1452528
|
C | T | 2 | a0002c0002t0008g0116a0006c0012t0037g0293 | 2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1544+1109C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452528 | ||||||
| chr11:1452529
|
G | A | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1544+1110G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452529 | ||||||
| chr11:1452592
|
G | A | 1 | a0002c0002t0058g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1544+1173G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452592 | ||||||
| chr11:1452592
|
GGATGCCT others(56): Show |
G | 1 | a0006c0012t0037g0293 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1544+1183_1544+124 others(67): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1452592 | |||||
| chr11:1452608
|
CCCACCCA others(56): Show |
C | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1544+1212_1544+127 others(67): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1452608 | |||||
| chr11:1452652
|
C | A | 87 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0048others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1544+1233C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452652 | ||||||
| chr11:1452701
|
G | A | 85 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0048others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1544+1282G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452701 | ||||||
| chr11:1452713
|
C | T | 3 | a0001c0001t0004g0081a0002c0002t0002g0118a0002c0002t0002g0119 | 3 | HG03834.hp1 NA18977.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1544+1294C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452713 | ||||||
| chr11:1452757
|
C | T | 88 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0048others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1544+1338C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452757 | ||||||
| chr11:1452843
|
C | T | 1 | a0001c0001t0062g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1544+1424C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452843 | ||||||
| chr11:1452850
|
G | T | 1 | a0001c0001t0009g0122 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1544+1431G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452850 | ||||||
| chr11:1452851
|
C | T | 87 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0048others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1544+1432C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452851 | ||||||
| chr11:1452929
|
A | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0097 | 2 | NA19005.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1544+1510A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452929 | ||||||
| chr11:1452931
|
G | A | 1 | a0002c0002t0005g0224 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1544+1512G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452931 | ||||||
| chr11:1452959
|
C | T | 1 | a0001c0003t0001g0070 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1545-1526C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452959 | ||||||
| chr11:1452964
|
A | G | 1 | a0001c0001t0003g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1545-1521A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452964 | ||||||
| chr11:1452980
|
G | A | 33 | a0001c0001t0001g0048a0001c0001t0001g0189a0001c0001t0001g0191others(30): Show | 33 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1545-1505G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1452980 | ||||||
| chr11:1453020
|
C | T | 1 | a0001c0001t0001g0343 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1545-1465C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453020 | ||||||
| chr11:1453084
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0141 | 2 | HG01496.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1545-1401C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453084 | ||||||
| chr11:1453141
|
C | T | 18 | a0001c0001t0001g0072a0001c0001t0003g0222a0001c0001t0003g0265others(15): Show | 19 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.1545-1344C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453141 | ||||||
| chr11:1453156
|
C | T | 41 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0048others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1545-1329C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453156 | ||||||
| chr11:1453197
|
TGTCCGGC others(26): Show |
T | 1 | a0001c0001t0006g0248 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1545-1285_1545-125 others(37): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1453197 | |||||
| chr11:1453215
|
A | G | 2 | a0001c0001t0028g0332a0001c0001t0028g0333 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1545-1270A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453215 | ||||||
| chr11:1453358
|
C | T | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0004g0173others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1545-1127C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453358 | ||||||
| chr11:1453407
|
T | C | 2 | a0001c0001t0018g0334a0001c0001t0067g0252 | 2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1545-1078T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453407 | ||||||
| chr11:1453538
|
C | T | 1 | a0002c0002t0049g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1545-947C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453538 | ||||||
| chr11:1453541
|
C | T | 2 | a0001c0003t0001g0115a0001c0003t0001g0146 | 2 | HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1545-944C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453541 | ||||||
| chr11:1453569
|
C | T | 3 | a0002c0002t0022g0003a0002c0002t0022g0204a0002c0002t0073g0217 | 4 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1545-916C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453569 | ||||||
| chr11:1453687
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1545-798C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453687 | ||||||
| chr11:1453731
|
G | GCC | 172 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(169): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1545-751_1545-750d others(4): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1453731 | |||||
| chr11:1453936
|
G | A | 55 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0057others(52): Show | 55 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1545-549G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453936 | ||||||
| chr11:1453948
|
G | A | 3 | a0001c0001t0009g0120a0001c0001t0009g0122a0001c0001t0009g0128 | 3 | NA18999.hp2 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1545-537G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453948 | ||||||
| chr11:1453961
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0043g0050 | 2 | HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1545-524T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453961 | ||||||
| chr11:1453967
|
T | G | 2 | a0001c0003t0026g0054a0001c0003t0026g0354 | 2 | NA18955.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1545-518T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1453967 | ||||||
| chr11:1454085
|
T | G | 1 | a0001c0001t0006g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1545-400T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454085 | ||||||
| chr11:1454154
|
G | C | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1545-331G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454154 | ||||||
| chr11:1454158
|
G | GGGAGGGC others(8): Show |
2 | a0002c0002t0012g0349a0002c0002t0039g0344 | 2 | NA18950.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1545-325_1545-324i others(17): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1454158 | |||||
| chr11:1454158
|
G | GGGGGGGC others(8): Show |
125 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0072others(122): Show | 126 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1545-309_1545-295d others(17): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1454158 | |||||
| chr11:1454158
|
G | GGGGGGGC others(23): Show |
5 | a0001c0001t0001g0048a0001c0001t0043g0050a0001c0001t0059g0041others(2): Show | 5 | HG02647.hp1 HG03017.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1545-324_1545-295d others(32): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1454158 | |||||
| chr11:1454158
|
G | GGGGGGGC others(38): Show |
2 | a0001c0003t0026g0054a0001c0003t0026g0354 | 2 | NA18955.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1545-295_1545-294i others(47): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1454158 | |||||
| chr11:1454158
|
G | GGGGGGGC others(8): Show |
1 | a0001c0001t0003g0239 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1545-319_1545-318i others(17): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1454158 | |||||
| chr11:1454158
|
G | GGGGGGGG others(9): Show |
1 | a0002c0002t0012g0347 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1545-321_1545-320i others(18): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1454158 | |||||
| chr11:1454158
|
GGGGGGGC others(8): Show |
G | 2 | a0001c0001t0001g0009a0001c0003t0004g0290 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1545-309_1545-295d others(17): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1454158 | |||||
| chr11:1454161
|
G | A | 1 | a0002c0002t0017g0301 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1545-324G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454161 | ||||||
| chr11:1454161
|
G | AGGGCTCA others(8): Show |
1 | a0002c0002t0012g0006 | 2 | NA19005.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1545-325_1545-324i others(17): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454161 | ||||||
| chr11:1454161
|
G | GGGGCTCA others(8): Show |
4 | a0002c0002t0002g0079a0002c0002t0007g0302a0002c0002t0007g0306others(1): Show | 4 | NA18990.hp2 NA18993.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1545-310_1545-309i others(17): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1454161 | |||||
| chr11:1454173
|
T | TGGGGGGC others(9): Show |
2 | a0002c0002t0038g0297a0002c0002t0040g0298 | 2 | HG02602.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1545-310_1545-295d others(18): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1454173 | |||||
| chr11:1454176
|
G | A | 16 | a0001c0001t0001g0067a0001c0001t0001g0082a0001c0001t0001g0097others(13): Show | 16 | HG00609.hp2 HG00673.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.1545-309G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454176 | ||||||
| chr11:1454176
|
G | GGGGCTCA others(8): Show |
21 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0044others(18): Show | 21 | HG00621.hp1 HG01070.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1545-305_1545-291d others(17): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1454176 | |||||
| chr11:1454176
|
G | GGGGCTCA others(23): Show |
42 | a0001c0001t0001g0010a0001c0001t0001g0052a0001c0001t0001g0053others(39): Show | 43 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.1545-295_1545-294i others(32): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 1454176 | |||||
| chr11:1454191
|
A | G | 15 | a0001c0001t0001g0087a0001c0001t0001g0107a0001c0001t0004g0080others(12): Show | 15 | HG00280.hp1 HG00673.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.1545-294A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454191 | ||||||
| chr11:1454249
|
C | T | 5 | a0001c0003t0003g0291a0002c0002t0016g0207a0002c0002t0016g0208others(2): Show | 5 | HG00642.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1545-236C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454249 | ||||||
| chr11:1454252
|
G | C | 2 | a0001c0001t0004g0314a0001c0001t0004g0316 | 2 | HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1545-233G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454252 | ||||||
| chr11:1454269
|
G | A | 44 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0044others(41): Show | 44 | HG00408.hp2 HG00609.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.1545-216G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454269 | ||||||
| chr11:1454370
|
G | A | 3 | a0002c0002t0002g0074a0002c0002t0002g0164a0002c0002t0002g0166 | 3 | HG00544.hp2 NA18980.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1545-115G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454370 | ||||||
| chr11:1454398
|
C | T | 48 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(45): Show | 48 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.1545-87C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454398 | ||||||
| chr11:1454416
|
T | A | 2 | a0001c0003t0001g0114a0001c0003t0001g0134 | 2 | NA18970.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1545-69T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454416 | ||||||
| chr11:1454418
|
C | A | 12 | a0002c0002t0002g0013a0002c0002t0002g0014a0002c0002t0002g0018others(9): Show | 12 | HG01109.hp2 HG01433.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1545-67C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454418 | ||||||
| chr11:1454419
|
G | T | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1545-66G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454419 | ||||||
| chr11:1454422
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1545-63G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454422 | ||||||
| chr11:1454476
|
A | G | 22 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0004g0051others(19): Show | 23 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1545-9A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 15/19 | chr11 | 1454476 | ||||||
| chr11:1454784
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0027g0129 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1668+176C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1454784 | ||||||
| chr11:1454829
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1668+221G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1454829 | ||||||
| chr11:1454880
|
C | G | 1 | a0002c0002t0017g0305 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1668+272C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1454880 | ||||||
| chr11:1454881
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0192others(1): Show | 4 | HG03130.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1668+273G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1454881 | ||||||
| chr11:1454881
|
G | C | 1 | a0002c0002t0017g0305 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1668+273G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1454881 | ||||||
| chr11:1455016
|
G | C | 1 | a0001c0001t0003g0002 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1668+408G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455016 | ||||||
| chr11:1455087
|
G | T | 2 | a0001c0003t0001g0114a0001c0003t0001g0134 | 2 | NA18970.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1668+479G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455087 | ||||||
| chr11:1455252
|
C | A | 1 | a0001c0003t0001g0331 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1668+644C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455252 | ||||||
| chr11:1455378
|
C | G | 1 | a0002c0002t0017g0305 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1668+770C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455378 | ||||||
| chr11:1455432
|
T | G | 140 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(137): Show | 142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1668+824T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455432 | ||||||
| chr11:1455461
|
C | T | 197 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(194): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1668+853C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455461 | ||||||
| chr11:1455612
|
C | T | 10 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0312others(7): Show | 10 | HG01070.hp2 HG02622.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1669-736C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455612 | ||||||
| chr11:1455635
|
G | A | 3 | a0002c0002t0019g0021a0002c0002t0019g0042a0002c0002t0019g0043 | 3 | HG02280.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1669-713G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455635 | ||||||
| chr11:1455680
|
C | T | 1 | a0001c0003t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1669-668C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455680 | ||||||
| chr11:1455774
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0192others(1): Show | 4 | HG03130.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1669-574C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455774 | ||||||
| chr11:1455778
|
T | C | 195 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(192): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1669-570T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455778 | ||||||
| chr11:1455838
|
C | T | 2 | a0002c0002t0008g0157a0002c0002t0008g0162 | 2 | HG00609.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1669-510C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455838 | ||||||
| chr11:1455850
|
T | C | 140 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(137): Show | 142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1669-498T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455850 | ||||||
| chr11:1455851
|
G | A | 140 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(137): Show | 142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1669-497G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455851 | ||||||
| chr11:1455887
|
C | T | 51 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(48): Show | 51 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1669-461C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455887 | ||||||
| chr11:1455901
|
G | A | 3 | a0001c0001t0003g0267a0001c0001t0003g0272a0001c0001t0025g0147 | 3 | HG00423.hp2 HG00558.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1669-447G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1455901 | ||||||
| chr11:1455930
|
GC | G | 96 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(93): Show | 97 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1669-414delC | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr11 | 1455930 | |||||
| chr11:1456011
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1669-337C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1456011 | ||||||
| chr11:1456132
|
C | T | 1 | a0002c0002t0007g0309 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1669-216C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 16/19 | chr11 | 1456132 | ||||||
| chr11:1456538
|
C | T | 49 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(46): Show | 49 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1849+10C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 17/19 | chr11 | 1456538 | ||||||
| chr11:1456567
|
C | T | 38 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0192others(35): Show | 39 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1850-31C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 17/19 | chr11 | 1456567 | ||||||
| chr11:1456575
|
G | T | 5 | a0002c0002t0002g0079a0002c0002t0005g0211a0002c0002t0007g0302others(2): Show | 5 | NA18990.hp2 NA18993.hp1 NA19070.hp1 others(2): Show |
intron_variant | MODIFIER | c.1850-23G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 17/19 | chr11 | 1456575 | ||||||
| chr11:1456752
|
G | T | 1 | a0001c0001t0004g0172 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1939+65G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1456752 | ||||||
| chr11:1456775
|
G | C | 1 | a0002c0002t0005g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1939+88G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1456775 | ||||||
| chr11:1456873
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0027g0129 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1939+186G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1456873 | ||||||
| chr11:1457104
|
G | A | 1 | a0001c0001t0004g0316 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1939+417G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457104 | ||||||
| chr11:1457217
|
G | C | 12 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0013g0022others(9): Show | 13 | HG01884.hp2 HG02630.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1939+530G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457217 | ||||||
| chr11:1457248
|
A | G | 141 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(138): Show | 143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1939+561A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457248 | ||||||
| chr11:1457290
|
C | T | 2 | a0001c0003t0001g0115a0001c0003t0001g0146 | 2 | HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1939+603C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457290 | ||||||
| chr11:1457322
|
T | A | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(90): Show | 94 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1939+635T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457322 | ||||||
| chr11:1457335
|
T | C | 244 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(241): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1939+648T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457335 | ||||||
| chr11:1457401
|
G | A | 3 | a0002c0002t0022g0003a0002c0002t0022g0204a0002c0002t0073g0217 | 4 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939+714G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457401 | ||||||
| chr11:1457408
|
A | G | 141 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(138): Show | 143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1939+721A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457408 | ||||||
| chr11:1457450
|
A | AG | 141 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(138): Show | 143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1939+763_1939+764i others(3): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457450 | ||||||
| chr11:1457598
|
G | A | 2 | a0002c0005t0034g0055a0002c0005t0034g0056 | 2 | HG01346.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1939+911G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457598 | ||||||
| chr11:1457612
|
C | T | 140 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(137): Show | 142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1939+925C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457612 | ||||||
| chr11:1457619
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1939+932C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457619 | ||||||
| chr11:1457704
|
T | A | 92 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(89): Show | 93 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1939+1017T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457704 | ||||||
| chr11:1457743
|
C | T | 141 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(138): Show | 143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1939+1056C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457743 | ||||||
| chr11:1457760
|
A | G | 143 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 145 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1939+1073A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457760 | ||||||
| chr11:1457808
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0027g0129 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1939+1121A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457808 | ||||||
| chr11:1457822
|
C | T | 30 | a0001c0001t0004g0136a0001c0001t0004g0161a0001c0001t0004g0172others(27): Show | 30 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1939+1135C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457822 | ||||||
| chr11:1457829
|
CGGGCTGG | C | 51 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(48): Show | 51 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1939+1149_1939+115 others(11): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr11 | 1457829 | |||||
| chr11:1457830
|
G | A | 1 | a0002c0002t0005g0274 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1939+1143G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457830 | ||||||
| chr11:1457886
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1939+1199G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457886 | ||||||
| chr11:1457893
|
A | G | 17 | a0001c0001t0046g0083a0002c0002t0008g0071a0002c0002t0008g0078others(14): Show | 18 | HG00408.hp2 HG00609.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.1939+1206A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457893 | ||||||
| chr11:1457936
|
T | C | 138 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(135): Show | 140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1939+1249T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457936 | ||||||
| chr11:1457936
|
T | G | 1 | a0001c0001t0004g0185 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1939+1249T>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457936 | ||||||
| chr11:1457962
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1940-1230C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457962 | ||||||
| chr11:1457979
|
G | A | 1 | a0002c0002t0030g0171 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1940-1213G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1457979 | ||||||
| chr11:1458076
|
C | T | 2 | a0001c0001t0018g0334a0001c0001t0067g0252 | 2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1940-1116C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458076 | ||||||
| chr11:1458157
|
A | G | 141 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(138): Show | 143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1940-1035A>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458157 | ||||||
| chr11:1458221
|
G | C | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1940-971G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458221 | ||||||
| chr11:1458371
|
T | C | 140 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(137): Show | 142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1940-821T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458371 | ||||||
| chr11:1458470
|
A | C | 1 | a0002c0002t0002g0132 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1940-722A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458470 | ||||||
| chr11:1458537
|
G | T | 1 | a0001c0001t0006g0218 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1940-655G>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458537 | ||||||
| chr11:1458558
|
C | T | 32 | a0001c0001t0001g0009a0001c0001t0001g0049a0001c0001t0003g0228others(29): Show | 33 | HG00408.hp2 HG00609.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1940-634C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458558 | ||||||
| chr11:1458629
|
G | A | 1 | a0001c0001t0006g0247 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1940-563G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458629 | ||||||
| chr11:1458751
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0077g0324 | 3 | HG03130.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1940-441G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458751 | ||||||
| chr11:1458755
|
C | G | 144 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 146 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1940-437C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458755 | ||||||
| chr11:1458793
|
G | A | 111 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(108): Show | 113 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1940-399G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458793 | ||||||
| chr11:1458902
|
C | T | 2 | a0002c0005t0034g0055a0002c0005t0034g0056 | 2 | HG01346.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1940-290C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458902 | ||||||
| chr11:1458923
|
G | C | 1 | a0001c0001t0001g0076 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1940-269G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458923 | ||||||
| chr11:1458937
|
G | A | 9 | a0001c0001t0001g0067a0001c0001t0003g0265a0001c0001t0003g0271others(6): Show | 9 | NA18947.hp1 NA18956.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1940-255G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1458937 | ||||||
| chr11:1459059
|
C | T | 4 | a0001c0001t0001g0049a0001c0001t0027g0129a0002c0005t0034g0055others(1): Show | 4 | HG01346.hp2 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1940-133C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1459059 | ||||||
| chr11:1459111
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0003g0280 | 2 | HG00438.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1940-81C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 18/19 | chr11 | 1459111 | ||||||
| chr11:1459286
|
C | T | 16 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0013g0022others(13): Show | 17 | HG00642.hp1 HG01884.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.1987+47C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1459286 | ||||||
| chr11:1459287
|
G | A | 2 | a0001c0001t0076g0182a0002c0002t0005g0198 | 2 | HG00735.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1987+48G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1459287 | ||||||
| chr11:1459296
|
C | T | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1987+57C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1459296 | ||||||
| chr11:1459310
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1987+71C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1459310 | ||||||
| chr11:1459407
|
A | C | 222 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0029others(219): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1987+168A>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1459407 | ||||||
| chr11:1459408
|
G | C | 222 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0029others(219): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1987+169G>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1459408 | ||||||
| chr11:1459499
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0062g0257 | 3 | HG01943.hp2 HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1987+260C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1459499 | ||||||
| chr11:1459529
|
G | A | 100 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0023others(97): Show | 102 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1987+290G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1459529 | ||||||
| chr11:1459615
|
G | A | 2 | a0002c0002t0005g0212a0004c0009t0008g0178 | 2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1987+376G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1459615 | ||||||
| chr11:1459768
|
G | A | 1 | a0001c0001t0003g0234 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1987+529G>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1459768 | ||||||
| chr11:1459901
|
C | T | 8 | a0001c0001t0018g0137a0001c0001t0018g0334a0001c0001t0021g0206others(5): Show | 8 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1988-599C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1459901 | ||||||
| chr11:1459913
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1988-587C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1459913 | ||||||
| chr11:1460065
|
C | T | 1 | a0001c0001t0075g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1988-435C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460065 | ||||||
| chr11:1460117
|
C | T | 1 | a0001c0001t0078g0205 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1988-383C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460117 | ||||||
| chr11:1460191
|
T | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1988-309T>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460191 | ||||||
| chr11:1460206
|
C | T | 1 | a0002c0002t0002g0014 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1988-294C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460206 | ||||||
| chr11:1460212
|
C | A | 1 | a0001c0001t0003g0234 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1988-288C>A | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460212 | ||||||
| chr11:1460272
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1988-228C>T | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460272 | ||||||
| chr11:1460380
|
T | C | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(196): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1988-120T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460380 | ||||||
| chr11:1460451
|
T | C | 4 | a0001c0001t0004g0175a0001c0001t0004g0179a0001c0001t0004g0180others(1): Show | 4 | HG01069.hp1 HG01361.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1988-49T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460451 | ||||||
| chr11:1460460
|
C | G | 8 | a0001c0001t0018g0137a0001c0001t0018g0334a0001c0001t0021g0206others(5): Show | 8 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1988-40C>G | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460460 | ||||||
| chr11:1460460
|
CCT | C | 25 | a0001c0001t0001g0130a0001c0001t0001g0317a0001c0001t0001g0343others(22): Show | 25 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.1988-39_1988-38del others(2): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460460 | ||||||
| chr11:1460460
|
CCTT | C | 154 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0023others(151): Show | 155 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1988-39_1988-37del others(3): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460460 | ||||||
| chr11:1460460
|
CCTTT | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0034others(14): Show | 18 | HG00280.hp2 HG00438.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1988-39_1988-36del others(4): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460460 | ||||||
| chr11:1460460
|
CCTTTTTT others(3): Show |
C | 1 | a0001c0003t0004g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1988-39_1988-30del others(10): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460460 | ||||||
| chr11:1460461
|
CT | C | 38 | a0001c0001t0001g0048a0001c0001t0018g0137a0001c0001t0018g0334others(35): Show | 39 | HG00323.hp2 HG00408.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1988-22delT | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr11 | 1460461 | |||||
| chr11:1460468
|
T | C | 1 | a0001c0001t0003g0227 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1988-32T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460468 | ||||||
| chr11:1460473
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1988-27T>C | BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 19/19 | chr11 | 1460473 |