Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23786 |
|---|---|
| ensemblid | ENSG00000099968.18 |
| hgncid | 17164 |
| symbol | BCL2L13 |
| name | BCL2 like 13 |
| refseq_nuc | NM_015367.4 |
| refseq_prot | NP_056182.2 |
| ensembl_nuc | ENST00000317582.10 |
| ensembl_prot | ENSP00000318883.5 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 17638757 |
| end | 17730855 |
| strand | + |
| ver | v1.2 |
| region | chr22:17638757-17730855 |
| region5000 | chr22:17633757-17735855 |
| regionname0 | BCL2L13_chr22_17638757_17730855 |
| regionname5000 | BCL2L13_chr22_17633757_17735855 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 485 | 264 | 80 | 44 | 92 | 13 | 33 | 71 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0002 | 0/0 | 485 | 19 | 4 | 11 | 0 | 3 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0003 | 0/0 | 485 | 13 | 2 | 8 | 1 | 0 | 2 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0004 | 0/0 | 485 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0005 | 0/0 | 485 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0006 | 0/0 | 485 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0007 | 0/0 | 485 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0008 | 0/0 | 485 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| 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 | 1458 | 200 | 60 | 34 | 79 | 7 | 19 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| c0002 | 1/0 | 1458 | 57 | 17 | 7 | 12 | 6 | 14 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| c0003 | 0/0 | 1458 | 19 | 4 | 11 | 0 | 3 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| c0004 | 0/0 | 1458 | 8 | 2 | 5 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| c0005 | 0/0 | 1458 | 5 | 0 | 3 | 1 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| c0006 | 0/0 | 1458 | 4 | 4 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| c0007 | 0/0 | 1458 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| c0008 | 0/0 | 1458 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| c0009 | 0/0 | 1458 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| c0010 | 0/0 | 1458 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| c0011 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| c0012 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| c0013 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| c0014 | 0/0 | 1458 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3502 | 46 | 6 | 17 | 9 | 2 | 11 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0002 | 0/1 | 3501 | 43 | 2 | 15 | 14 | 3 | 8 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0003 | 0/0 | 3503 | 35 | 13 | 0 | 21 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0004 | 0/0 | 3502 | 21 | 1 | 3 | 11 | 2 | 4 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0005 | 0/0 | 3502 | 19 | 7 | 2 | 8 | 0 | 2 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0006 | 0/0 | 3502 | 17 | 4 | 4 | 2 | 3 | 4 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0007 | 0/0 | 3503 | 12 | 11 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0008 | 0/0 | 3503 | 8 | 4 | 1 | 2 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0009 | 0/0 | 3508 | 6 | 2 | 4 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0010 | 0/0 | 3504 | 5 | 0 | 1 | 4 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0011 | 0/0 | 3503 | 5 | 0 | 1 | 4 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0012 | 0/0 | 3503 | 4 | 4 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0013 | 0/0 | 3502 | 4 | 0 | 0 | 4 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0014 | 0/0 | 3502 | 4 | 4 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0015 | 0/0 | 3502 | 3 | 0 | 3 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0016 | 0/0 | 3502 | 3 | 1 | 1 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0017 | 0/0 | 3503 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0018 | 0/0 | 3501 | 3 | 0 | 1 | 2 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0019 | 0/0 | 3503 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0020 | 0/0 | 3508 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0021 | 0/0 | 3503 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0022 | 0/0 | 3503 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0023 | 0/0 | 3503 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0024 | 0/0 | 3503 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0025 | 0/0 | 3502 | 2 | 0 | 0 | 0 | 2 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0026 | 0/0 | 3503 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0027 | 0/0 | 3502 | 2 | 1 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0028 | 0/0 | 3503 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0029 | 0/0 | 3502 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0030 | 0/0 | 3502 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0031 | 0/0 | 3502 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0032 | 0/0 | 3502 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0033 | 0/0 | 3501 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0034 | 0/0 | 3502 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0035 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0036 | 0/0 | 3504 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0037 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0038 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0039 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0040 | 0/0 | 3502 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0041 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0042 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0043 | 0/0 | 3503 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0044 | 0/0 | 3508 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0045 | 0/0 | 3501 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0046 | 0/0 | 3504 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0047 | 0/0 | 3502 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0048 | 0/0 | 3502 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0049 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0050 | 0/0 | 3502 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0051 | 0/0 | 3502 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0052 | 0/0 | 3502 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0053 | 0/0 | 3501 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0054 | 0/0 | 3501 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0055 | 0/0 | 3502 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0056 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0057 | 0/0 | 3501 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0058 | 0/0 | 3502 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0059 | 0/0 | 3502 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0060 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0061 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0062 | 0/0 | 3502 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0063 | 0/0 | 3502 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0064 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0065 | 0/0 | 3502 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0066 | 0/0 | 3502 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0067 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0068 | 0/0 | 3503 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| t0069 | 0/0 | 3502 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| 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 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| 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 | 1458 | 200 | 60 | 34 | 79 | 7 | 19 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002 | 1/0 | 1458 | 57 | 17 | 7 | 12 | 6 | 14 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0007 | 0/0 | 1458 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0009 | 0/0 | 1458 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0012 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0014 | 0/0 | 1458 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0002c0003 | 0/0 | 1458 | 19 | 4 | 11 | 0 | 3 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0003c0004 | 0/0 | 1458 | 8 | 2 | 5 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0003c0005 | 0/0 | 1458 | 5 | 0 | 3 | 1 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0004c0006 | 0/0 | 1458 | 4 | 4 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0005c0008 | 0/0 | 1458 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0006c0010 | 0/0 | 1458 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0007c0013 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0008c0011 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/1 | 4958 | 42 | 2 | 15 | 13 | 3 | 8 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0003 | 0/0 | 4960 | 34 | 12 | 0 | 21 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0004 | 0/0 | 4959 | 19 | 1 | 1 | 11 | 2 | 4 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0005 | 0/0 | 4959 | 19 | 7 | 2 | 8 | 0 | 2 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0006 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0007 | 0/0 | 4960 | 11 | 11 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0008 | 0/0 | 4960 | 8 | 4 | 1 | 2 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0009 | 0/0 | 4965 | 4 | 0 | 4 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0010 | 0/0 | 4961 | 5 | 0 | 1 | 4 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0011 | 0/0 | 4960 | 5 | 0 | 1 | 4 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0013 | 0/0 | 4959 | 4 | 0 | 0 | 4 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0017 | 0/0 | 4960 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0018 | 0/0 | 4958 | 3 | 0 | 1 | 2 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0020 | 0/0 | 4965 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0021 | 0/0 | 4960 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0022 | 0/0 | 4960 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0023 | 0/0 | 4960 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0024 | 0/0 | 4960 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0028 | 0/0 | 4960 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0029 | 0/0 | 4959 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0032 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0033 | 0/0 | 4958 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0034 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0036 | 0/0 | 4961 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0038 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0039 | 0/0 | 4958 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0040 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0041 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0043 | 0/0 | 4960 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0046 | 0/0 | 4961 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0047 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0048 | 0/0 | 4959 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0050 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0051 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0053 | 0/0 | 4958 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0054 | 0/0 | 4958 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0055 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0056 | 0/0 | 4958 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0057 | 0/0 | 4958 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0060 | 0/0 | 4964 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0061 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0062 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0064 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0065 | 0/0 | 4959 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0066 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0067 | 0/0 | 4958 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0001t0068 | 0/0 | 4960 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002t0001 | 1/0 | 4959 | 26 | 0 | 5 | 9 | 1 | 10 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002t0006 | 0/0 | 4959 | 11 | 3 | 1 | 1 | 3 | 3 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002t0012 | 0/0 | 4960 | 4 | 4 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002t0014 | 0/0 | 4959 | 4 | 4 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002t0025 | 0/0 | 4959 | 2 | 0 | 0 | 0 | 2 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002t0026 | 0/0 | 4960 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002t0027 | 0/0 | 4959 | 2 | 1 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002t0035 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002t0037 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002t0042 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002t0045 | 0/0 | 4958 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002t0052 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0002t0069 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0007t0009 | 0/0 | 4965 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0007t0044 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0009t0004 | 0/0 | 4959 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0012t0002 | 0/0 | 4958 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0001c0014t0007 | 0/0 | 4960 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0002c0003t0001 | 0/0 | 4959 | 17 | 4 | 11 | 0 | 1 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0002c0003t0058 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0002c0003t0059 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0003c0004t0015 | 0/0 | 4959 | 3 | 0 | 3 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0003c0004t0016 | 0/0 | 4959 | 3 | 1 | 1 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0003c0004t0030 | 0/0 | 4959 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0003c0004t0031 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0003c0005t0006 | 0/0 | 4959 | 5 | 0 | 3 | 1 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0004c0006t0001 | 0/0 | 4959 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0004c0006t0049 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0004c0006t0063 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0005c0008t0019 | 0/0 | 4960 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0006c0010t0001 | 0/0 | 4959 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0007c0013t0003 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| a0008c0011t0023 | 0/0 | 4960 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | copy fasta | chr22 | 17633757 | 17735855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0009g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0009g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0009g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0009g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0010g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0010g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0010g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0010g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0010g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0011g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0011g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0011g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0011g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0011g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0013g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0013g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0013g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0013g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0017g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0017g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0017g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0018g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0018g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0018g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0020g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0020g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0020g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0021g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0021g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0021g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0022g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0022g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0023g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0024g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0024g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0028g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0028g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0029g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0029g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0032g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0033g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0034g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0036g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0038g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0039g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0040g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0041g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0043g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0046g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0047g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0048g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0050g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0051g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0053g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0054g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0055g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0056g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0057g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0060g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0061g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0062g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0064g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0065g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0066g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0067g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0068g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0012g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0012g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0012g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0012g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0014g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0014g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0014g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0014g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0025g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0025g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0026g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0026g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0027g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0027g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0035g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0037g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0042g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0045g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0052g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0069g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0007t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0007t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0007t0044g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0009t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0009t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0012t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0014t0007g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0058g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0059g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0015g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0015g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0015g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0016g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0016g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0016g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0030g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0031g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0005t0006g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0005t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0005t0006g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0005t0006g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0005t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0004c0006t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0004c0006t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0004c0006t0049g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0004c0006t0063g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0005c0008t0019g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0005c0008t0019g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0005c0008t0019g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0006c0010t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0007c0013t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0008c0011t0023g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0186 | EUR | GBR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00099 | hp2 | a0001 | c0002 | t0006 | g0102 | EUR | GBR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00140 | hp1 | a0002 | c0003 | t0058 | g0275 | EUR | GBR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00140 | hp2 | a0001 | c0001 | t0043 | g0001 | EUR | GBR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0188 | EUR | FIN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00280 | hp2 | a0002 | c0003 | t0001 | g0271 | EUR | FIN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00323 | hp1 | a0001 | c0001 | t0047 | g0135 | EUR | FIN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0119 | EUR | FIN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0241 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00408 | hp2 | a0001 | c0002 | t0069 | g0294 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00423 | hp1 | a0003 | c0005 | t0006 | g0083 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00423 | hp2 | a0001 | c0001 | t0051 | g0205 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0153 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00438 | hp2 | a0001 | c0001 | t0018 | g0207 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00544 | hp1 | a0001 | c0001 | t0018 | g0206 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0173 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00609 | hp2 | a0001 | c0001 | t0029 | g0174 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0260 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00733 | hp1 | a0001 | c0001 | t0009 | g0040 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00733 | hp2 | a0002 | c0003 | t0001 | g0262 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00735 | hp1 | a0001 | c0001 | t0033 | g0137 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00735 | hp2 | a0002 | c0003 | t0001 | g0276 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00738 | hp1 | a0001 | c0002 | t0006 | g0066 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0242 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0286 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0268 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0280 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0279 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01074 | hp2 | a0003 | c0005 | t0006 | g0085 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01081 | hp1 | a0003 | c0005 | t0006 | g0086 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01081 | hp2 | a0001 | c0001 | t0053 | g0139 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0145 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01109 | hp2 | a0003 | c0004 | t0015 | g0253 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01167 | hp1 | a0001 | c0001 | t0022 | g0237 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01167 | hp2 | a0001 | c0001 | t0018 | g0171 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0267 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01168 | hp2 | a0001 | c0001 | t0009 | g0032 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01169 | hp1 | a0002 | c0003 | t0001 | g0266 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01169 | hp2 | a0001 | c0001 | t0022 | g0239 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01175 | hp2 | a0003 | c0004 | t0030 | g0101 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01192 | hp1 | a0001 | c0014 | t0007 | g0010 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01243 | hp1 | a0001 | c0001 | t0046 | g0023 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01243 | hp2 | a0001 | c0001 | t0048 | g0140 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0272 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01255 | hp2 | a0001 | c0001 | t0065 | g0103 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01256 | hp1 | a0001 | c0009 | t0004 | g0158 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01258 | hp1 | a0001 | c0009 | t0004 | g0157 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01258 | hp2 | a0002 | c0003 | t0001 | g0292 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01261 | hp2 | a0001 | c0002 | t0027 | g0006 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0192 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0297 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01361 | hp1 | a0003 | c0005 | t0006 | g0082 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01361 | hp2 | a0001 | c0001 | t0011 | g0133 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0234 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01496 | hp2 | a0001 | c0001 | t0009 | g0033 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0191 | EUR | IBS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01516 | hp2 | a0001 | c0002 | t0025 | g0074 | EUR | IBS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01517 | hp1 | a0002 | c0003 | t0059 | g0273 | EUR | IBS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01517 | hp2 | a0001 | c0002 | t0025 | g0075 | EUR | IBS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01884 | hp1 | a0001 | c0002 | t0012 | g0004 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01884 | hp2 | a0003 | c0004 | t0031 | g0254 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01934 | hp2 | a0003 | c0004 | t0016 | g0087 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01978 | hp2 | a0001 | c0001 | t0010 | g0238 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01981 | hp1 | a0001 | c0001 | t0009 | g0038 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01981 | hp2 | a0002 | c0003 | t0001 | g0278 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0281 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02040 | hp2 | a0001 | c0002 | t0052 | g0285 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02055 | hp1 | a0003 | c0004 | t0016 | g0089 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02055 | hp2 | a0001 | c0002 | t0012 | g0305 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02071 | hp1 | a0001 | c0002 | t0006 | g0077 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0148 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0070 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02145 | hp2 | a0001 | c0002 | t0027 | g0076 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02148 | hp2 | a0003 | c0004 | t0015 | g0080 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | CDX | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | CDX | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02257 | hp1 | a0001 | c0001 | t0020 | g0233 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0060 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02258 | hp1 | a0001 | c0002 | t0035 | g0301 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0096 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02280 | hp1 | a0001 | c0002 | t0012 | g0306 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02280 | hp2 | a0004 | c0006 | t0063 | g0093 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02300 | hp1 | a0001 | c0001 | t0054 | g0183 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02300 | hp2 | a0003 | c0004 | t0015 | g0081 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0149 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02451 | hp2 | a0001 | c0001 | t0050 | g0250 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02572 | hp1 | a0001 | c0001 | t0028 | g0303 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02602 | hp1 | a0001 | c0001 | t0057 | g0125 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02602 | hp2 | a0001 | c0002 | t0006 | g0068 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02615 | hp1 | a0001 | c0001 | t0021 | g0018 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02615 | hp2 | a0002 | c0003 | t0001 | g0221 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02622 | hp1 | a0001 | c0002 | t0026 | g0299 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02647 | hp1 | a0001 | c0001 | t0028 | g0302 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02683 | hp1 | a0001 | c0001 | t0040 | g0187 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0265 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0247 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02698 | hp2 | a0001 | c0001 | t0008 | g0227 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02717 | hp1 | a0001 | c0002 | t0014 | g0065 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0248 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02723 | hp1 | a0001 | c0001 | t0041 | g0240 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0201 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0124 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02809 | hp2 | a0001 | c0002 | t0006 | g0072 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02818 | hp2 | a0001 | c0001 | t0020 | g0224 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02886 | hp1 | a0004 | c0006 | t0049 | g0091 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02886 | hp2 | a0002 | c0003 | t0001 | g0220 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02895 | hp1 | a0001 | c0001 | t0021 | g0014 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02895 | hp2 | a0001 | c0001 | t0024 | g0243 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02896 | hp1 | a0001 | c0001 | t0062 | g0110 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02896 | hp2 | a0001 | c0002 | t0014 | g0063 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02897 | hp1 | a0001 | c0001 | t0024 | g0244 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02897 | hp2 | a0001 | c0002 | t0014 | g0061 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02922 | hp1 | a0007 | c0013 | t0003 | g0028 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02922 | hp2 | a0001 | c0002 | t0006 | g0078 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02965 | hp2 | a0005 | c0008 | t0019 | g0255 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0218 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0182 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0282 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0229 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03041 | hp2 | a0001 | c0001 | t0017 | g0019 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03130 | hp1 | a0001 | c0001 | t0017 | g0020 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03130 | hp2 | a0001 | c0007 | t0009 | g0053 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0109 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0226 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03225 | hp1 | a0004 | c0006 | t0001 | g0090 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03225 | hp2 | a0001 | c0007 | t0009 | g0056 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0127 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03453 | hp2 | a0001 | c0002 | t0026 | g0300 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03486 | hp1 | a0001 | c0002 | t0012 | g0003 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03490 | hp1 | a0002 | c0003 | t0001 | g0270 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0295 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03492 | hp2 | a0003 | c0005 | t0006 | g0084 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03516 | hp1 | a0004 | c0006 | t0001 | g0092 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0197 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03540 | hp1 | a0005 | c0008 | t0019 | g0298 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03579 | hp1 | a0001 | c0002 | t0006 | g0071 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03654 | hp1 | a0003 | c0004 | t0016 | g0088 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03654 | hp2 | a0001 | c0002 | t0006 | g0069 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0142 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03710 | hp2 | a0001 | c0002 | t0006 | g0073 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0264 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0200 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0290 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0123 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0155 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | STU | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0095 | SAS | STU | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0261 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | STU | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0130 | SAS | STU | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0283 | SAS | STU | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | STU | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | YRI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18522 | hp2 | a0001 | c0001 | t0017 | g0013 | AFR | YRI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | CHB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | CHB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18906 | hp1 | a0005 | c0008 | t0019 | g0256 | AFR | YRI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | YRI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18942 | hp1 | a0001 | c0001 | t0039 | g0160 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18943 | hp2 | a0001 | c0001 | t0013 | g0184 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18946 | hp2 | a0001 | c0001 | t0036 | g0094 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18952 | hp2 | a0001 | c0001 | t0010 | g0225 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18953 | hp2 | a0001 | c0001 | t0010 | g0235 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18956 | hp2 | a0001 | c0001 | t0008 | g0230 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18957 | hp1 | a0001 | c0001 | t0011 | g0113 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18963 | hp1 | a0001 | c0001 | t0067 | g0170 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18964 | hp2 | a0001 | c0001 | t0056 | g0214 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18968 | hp2 | a0008 | c0011 | t0023 | g0106 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18979 | hp2 | a0001 | c0001 | t0013 | g0236 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0185 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18998 | hp1 | a0001 | c0001 | t0011 | g0151 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19003 | hp2 | a0001 | c0001 | t0011 | g0180 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19007 | hp2 | a0001 | c0001 | t0013 | g0165 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19009 | hp1 | a0001 | c0001 | t0023 | g0105 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19030 | hp1 | a0001 | c0002 | t0037 | g0062 | AFR | LWK | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0249 | AFR | LWK | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0232 | AFR | LWK | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0274 | AFR | LWK | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19056 | hp2 | a0001 | c0012 | t0002 | g0159 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19065 | hp2 | a0001 | c0001 | t0068 | g0152 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19078 | hp2 | a0001 | c0001 | t0010 | g0219 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19079 | hp1 | a0001 | c0001 | t0013 | g0164 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19079 | hp2 | a0001 | c0001 | t0008 | g0223 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19085 | hp1 | a0001 | c0001 | t0011 | g0167 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19089 | hp1 | a0001 | c0001 | t0060 | g0178 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19089 | hp2 | a0001 | c0001 | t0010 | g0146 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19090 | hp2 | a0001 | c0001 | t0029 | g0193 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19240 | hp1 | a0001 | c0002 | t0014 | g0064 | AFR | YRI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19240 | hp2 | a0001 | c0007 | t0044 | g0052 | AFR | YRI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20129 | hp1 | a0001 | c0001 | t0038 | g0228 | AFR | ASW | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20129 | hp2 | a0001 | c0002 | t0042 | g0005 | AFR | ASW | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20752 | hp1 | a0001 | c0002 | t0006 | g0079 | EUR | TSI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0141 | EUR | TSI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20805 | hp1 | a0001 | c0002 | t0006 | g0067 | EUR | TSI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0131 | EUR | TSI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20905 | hp1 | a0001 | c0002 | t0045 | g0121 | SAS | GIH | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20905 | hp2 | a0001 | c0001 | t0032 | g0166 | SAS | GIH | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01123 | hp1 | a0006 | c0010 | t0001 | g0263 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0277 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02109 | hp1 | a0001 | c0001 | t0064 | g0304 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02109 | hp2 | a0001 | c0001 | t0066 | g0011 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0269 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0222 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02559 | hp1 | a0001 | c0001 | t0021 | g0015 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02559 | hp2 | a0001 | c0001 | t0055 | g0129 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03471 | hp1 | a0001 | c0001 | t0061 | g0016 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0118 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | USA | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0098 | AFR | USA | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | USA | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | USA | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA21309 | hp1 | a0001 | c0001 | t0020 | g0231 | AFR | LWK | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA21309 | hp2 | a0001 | c0001 | t0034 | g0181 | AFR | LWK | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0212 | REF | REF | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0122 | REF | REF | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:17683229
|
T | G | 1 | a0003 | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
missense_variant | MODERATE | c.137T>G | p.Ile46Arg | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/7 | 317/4959 | 137/1458 | 46/485 | chr22 | 17683229 | ||
| chr22:17683255
|
A | G | 1 | a0004 | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.163A>G | p.Ile55Val | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/7 | 343/4959 | 163/1458 | 55/485 | chr22 | 17683255 | ||
| chr22:17689010
|
G | A | 1 | a0006 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.254G>A | p.Arg85His | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/7 | 434/4959 | 254/1458 | 85/485 | chr22 | 17689010 | ||
| chr22:17702357
|
G | T | 1 | a0005 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.571G>T | p.Ala191Ser | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/7 | 751/4959 | 571/1458 | 191/485 | chr22 | 17702357 | ||
| chr22:17727154
|
C | T | 1 | a0002 | 19 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(16): Show |
missense_variant | MODERATE | c.1078C>T | p.Pro360Ser | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1258/4959 | 1078/1458 | 360/485 | chr22 | 17727154 | ||
| chr22:17727286
|
C | A | 1 | a0008 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.1210C>A | p.Pro404Thr | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1390/4959 | 1210/1458 | 404/485 | chr22 | 17727286 | ||
| chr22:17727361
|
A | G | 1 | a0007 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1285A>G | p.Ser429Gly | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1465/4959 | 1285/1458 | 429/485 | chr22 | 17727361 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:17702272
|
A | G | 1 | a0001c0009 | 2 | HG01256.hp1 HG01258.hp1 |
synonymous_variant | LOW | c.486A>G | p.Gln162Gln | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/7 | 666/4959 | 486/1458 | 162/485 | chr22 | 17702272 | ||
| chr22:17726730
|
A | G | 1 | a0001c0007 | 3 | HG03130.hp2 HG03225.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.654A>G | p.Ala218Ala | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 834/4959 | 654/1458 | 218/485 | chr22 | 17726730 | ||
| chr22:17726847
|
A | G | 7 | a0001c0001a0001c0007a0001c0009others(4): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
synonymous_variant | LOW | c.771A>G | p.Ser257Ser | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 951/4959 | 771/1458 | 257/485 | chr22 | 17726847 | ||
| chr22:17726952
|
C | T | 1 | a0003c0004 | 8 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(5): Show |
synonymous_variant | LOW | c.876C>T | p.Asn292Asn | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1056/4959 | 876/1458 | 292/485 | chr22 | 17726952 | ||
| chr22:17727003
|
C | T | 1 | a0001c0014 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.927C>T | p.His309His | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1107/4959 | 927/1458 | 309/485 | chr22 | 17727003 | ||
| chr22:17727411
|
C | T | 1 | a0001c0012 | 1 | NA19056.hp2 | synonymous_variant | LOW | c.1335C>T | p.Pro445Pro | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1515/4959 | 1335/1458 | 445/485 | chr22 | 17727411 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:17638807
|
C | T | 1 | a0001c0002t0069 | 1 | HG00408.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/7 | 16905 | chr22 | 17638807 | |||||
| chr22:17655675
|
A | G | 1 | a0001c0001t0068 | 1 | NA19065.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/7 | 37 | chr22 | 17655675 | |||||
| chr22:17727643
|
T | G | 1 | a0003c0004t0030 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 109 | chr22 | 17727643 | |||||
| chr22:17727706
|
C | T | 1 | a0001c0001t0067 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*172C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 172 | chr22 | 17727706 | |||||
| chr22:17727739
|
C | T | 1 | a0001c0001t0066 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*205C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 205 | chr22 | 17727739 | |||||
| chr22:17727788
|
C | T | 2 | a0001c0001t0064a0001c0001t0065 | 2 | HG01255.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*254C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 254 | chr22 | 17727788 | |||||
| chr22:17727794
|
T | G | 6 | a0001c0001t0032a0001c0001t0033a0003c0004t0015others(3): Show | 10 | HG00735.hp1 HG01109.hp2 HG01175.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*260T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 260 | chr22 | 17727794 | |||||
| chr22:17727852
|
G | A | 3 | a0003c0004t0015a0003c0004t0030a0003c0004t0031 | 5 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*318G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 318 | chr22 | 17727852 | |||||
| chr22:17727900
|
G | A | 1 | a0001c0001t0034 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*366G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 366 | chr22 | 17727900 | |||||
| chr22:17727938
|
G | C | 36 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(33): Show | 121 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*404G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 404 | chr22 | 17727938 | |||||
| chr22:17728034
|
TG | T | 5 | a0001c0002t0045a0003c0004t0015a0003c0004t0016others(2): Show | 9 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*503delG | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 503 | INFO_REALIGN_3_PRIME | chr22 | 17728034 | ||||
| chr22:17728056
|
C | G | 14 | a0001c0001t0009a0001c0001t0020a0001c0001t0021others(11): Show | 26 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*522C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 522 | chr22 | 17728056 | |||||
| chr22:17728099
|
A | AGGCTG | 5 | a0001c0001t0009a0001c0001t0020a0001c0001t0060others(2): Show | 11 | HG00733.hp1 HG01168.hp2 HG01496.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*569_*570insGGGCT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 570 | INFO_REALIGN_3_PRIME | chr22 | 17728099 | ||||
| chr22:17728130
|
G | C | 2 | a0001c0002t0035a0003c0004t0031 | 2 | HG01884.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*596G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 596 | chr22 | 17728130 | |||||
| chr22:17728130
|
G | GC | 8 | a0001c0001t0010a0001c0001t0022a0001c0001t0028others(5): Show | 15 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*599dupC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 600 | INFO_REALIGN_3_PRIME | chr22 | 17728130 | ||||
| chr22:17728211
|
G | C | 2 | a0001c0001t0023a0008c0011t0023 | 2 | NA18968.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*677G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 677 | chr22 | 17728211 | |||||
| chr22:17728212
|
T | C | 1 | a0001c0002t0037 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*678T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 678 | chr22 | 17728212 | |||||
| chr22:17728254
|
G | GA | 34 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(31): Show | 112 | HG00140.hp2 HG00733.hp1 HG01109.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*720_*721insA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 721 | chr22 | 17728254 | |||||
| chr22:17728255
|
T | C | 34 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(31): Show | 112 | HG00140.hp2 HG00733.hp1 HG01109.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*721T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 721 | chr22 | 17728255 | |||||
| chr22:17728266
|
C | T | 1 | a0002c0003t0059 | 1 | HG01517.hp1 | 3_prime_UTR_variant | MODIFIER | c.*732C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 732 | chr22 | 17728266 | |||||
| chr22:17728269
|
G | A | 1 | a0001c0001t0022 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*735G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 735 | chr22 | 17728269 | |||||
| chr22:17728419
|
G | C | 6 | a0001c0001t0008a0001c0001t0010a0001c0001t0020others(3): Show | 20 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*885G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 885 | chr22 | 17728419 | |||||
| chr22:17728439
|
T | C | 36 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(33): Show | 139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*905T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 905 | chr22 | 17728439 | |||||
| chr22:17728526
|
A | G | 1 | a0005c0008t0019 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*992A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 992 | chr22 | 17728526 | |||||
| chr22:17728567
|
A | G | 1 | a0001c0001t0040 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1033A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1033 | chr22 | 17728567 | |||||
| chr22:17728601
|
A | G | 1 | a0001c0001t0039 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1067A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1067 | chr22 | 17728601 | |||||
| chr22:17728752
|
A | C | 1 | a0001c0001t0057 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1218A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1218 | chr22 | 17728752 | |||||
| chr22:17728875
|
C | G | 1 | a0002c0003t0058 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1341C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1341 | chr22 | 17728875 | |||||
| chr22:17728999
|
G | A | 1 | a0001c0001t0050 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1465G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1465 | chr22 | 17728999 | |||||
| chr22:17729191
|
A | G | 1 | a0001c0001t0056 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1657A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1657 | chr22 | 17729191 | |||||
| chr22:17729217
|
T | C | 7 | a0001c0001t0004a0001c0001t0011a0001c0001t0032others(4): Show | 30 | HG00423.hp2 HG00438.hp1 HG01256.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1683T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1683 | chr22 | 17729217 | |||||
| chr22:17729569
|
C | T | 1 | a0005c0008t0019 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2035C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2035 | chr22 | 17729569 | |||||
| chr22:17729764
|
C | T | 14 | a0001c0001t0003a0001c0001t0008a0001c0001t0009others(11): Show | 65 | HG00140.hp2 HG00733.hp1 HG01167.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2230C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2230 | chr22 | 17729764 | |||||
| chr22:17729765
|
G | A | 6 | a0001c0001t0006a0001c0002t0006a0001c0002t0014others(3): Show | 24 | HG00099.hp2 HG00423.hp1 HG00738.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2231G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2231 | chr22 | 17729765 | |||||
| chr22:17729865
|
G | A | 1 | a0001c0002t0052 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2331G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2331 | chr22 | 17729865 | |||||
| chr22:17729986
|
G | T | 1 | a0001c0001t0055 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2452G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2452 | chr22 | 17729986 | |||||
| chr22:17730010
|
GC | G | 12 | a0001c0001t0002a0001c0001t0018a0001c0001t0033others(9): Show | 55 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2478delC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2478 | INFO_REALIGN_3_PRIME | chr22 | 17730010 | ||||
| chr22:17730029
|
A | G | 1 | a0001c0007t0044 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2495A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2495 | chr22 | 17730029 | |||||
| chr22:17730089
|
G | A | 1 | a0001c0001t0053 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2555G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2555 | chr22 | 17730089 | |||||
| chr22:17730157
|
A | G | 4 | a0003c0004t0015a0003c0004t0016a0003c0004t0030others(1): Show | 8 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2623A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2623 | chr22 | 17730157 | |||||
| chr22:17730291
|
G | A | 34 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(31): Show | 136 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*2757G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2757 | chr22 | 17730291 | |||||
| chr22:17730427
|
C | T | 1 | a0001c0001t0051 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2893C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2893 | chr22 | 17730427 | |||||
| chr22:17730544
|
G | A | 1 | a0001c0001t0054 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3010G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 3010 | chr22 | 17730544 | |||||
| chr22:17730797
|
C | T | 3 | a0001c0001t0028a0001c0001t0029a0001c0001t0046 | 5 | HG00609.hp2 HG01243.hp1 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3263C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 3263 | chr22 | 17730797 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:17638965
|
C | T | 2 | a0001c0002t0012g0305a0001c0002t0012g0306 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-51+79C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17638965 | ||||||
| chr22:17638971
|
G | C | 1 | a0001c0001t0043g0001 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-51+85G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17638971 | ||||||
| chr22:17638979
|
G | A | 1 | a0001c0001t0003g0002 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-51+93G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17638979 | ||||||
| chr22:17639069
|
C | T | 1 | a0001c0001t0064g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-51+183C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639069 | ||||||
| chr22:17639092
|
G | C | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+206G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639092 | ||||||
| chr22:17639116
|
G | A | 1 | a0001c0002t0027g0006 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-51+230G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639116 | ||||||
| chr22:17639244
|
ACTT | A | 47 | a0001c0001t0002g0295a0001c0001t0002g0296a0001c0001t0028g0302others(44): Show | 47 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.-51+362_-51+364del others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17639244 | |||||
| chr22:17639332
|
G | A | 3 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259 | 3 | HG00544.hp2 NA18942.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.-51+446G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639332 | ||||||
| chr22:17639341
|
A | G | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+455A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639341 | ||||||
| chr22:17639414
|
C | T | 2 | a0003c0004t0015g0253a0003c0004t0031g0254 | 2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-51+528C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639414 | ||||||
| chr22:17639434
|
C | T | 2 | a0001c0001t0003g0251a0001c0001t0003g0252 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-51+548C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639434 | ||||||
| chr22:17639474
|
A | G | 3 | a0001c0001t0007g0248a0001c0001t0007g0249a0001c0001t0050g0250 | 3 | HG02451.hp2 HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-51+588A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639474 | ||||||
| chr22:17639611
|
C | T | 1 | a0001c0002t0001g0247 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-51+725C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639611 | ||||||
| chr22:17639646
|
C | G | 1 | a0001c0001t0004g0246 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-51+760C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639646 | ||||||
| chr22:17639684
|
G | C | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+798G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639684 | ||||||
| chr22:17639687
|
C | G | 1 | a0001c0001t0002g0245 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-51+801C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639687 | ||||||
| chr22:17639690
|
C | T | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-51+804C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639690 | ||||||
| chr22:17639718
|
T | C | 14 | a0001c0001t0005g0007a0001c0001t0007g0008a0001c0001t0007g0009others(11): Show | 14 | HG01192.hp1 HG02109.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-51+832T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639718 | ||||||
| chr22:17639720
|
G | A | 150 | a0001c0001t0002g0295a0001c0001t0002g0296a0001c0001t0003g0002others(147): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-51+834G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639720 | ||||||
| chr22:17639856
|
C | CT | 53 | a0001c0001t0002g0295a0001c0001t0002g0296a0001c0001t0005g0241others(50): Show | 53 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.-51+985dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17639856 | |||||
| chr22:17639856
|
C | CTT | 6 | a0001c0001t0024g0243a0001c0001t0024g0244a0001c0002t0026g0299others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51+984_-51+985dup others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17639856 | |||||
| chr22:17639856
|
CT | C | 48 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0003g0002others(45): Show | 48 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.-51+985delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17639856 | |||||
| chr22:17640043
|
G | A | 25 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(22): Show | 25 | HG00738.hp1 HG01261.hp2 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51+1157G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640043 | ||||||
| chr22:17640171
|
AC | A | 25 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(22): Show | 25 | HG00738.hp1 HG01261.hp2 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51+1290delC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17640171 | |||||
| chr22:17640192
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+1306G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640192 | ||||||
| chr22:17640228
|
G | A | 12 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(9): Show | 12 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+1342G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640228 | ||||||
| chr22:17640229
|
T | G | 12 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(9): Show | 12 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+1343T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640229 | ||||||
| chr22:17640270
|
A | G | 24 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(21): Show | 24 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.-51+1384A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640270 | ||||||
| chr22:17640339
|
G | A | 1 | a0001c0002t0001g0261 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-51+1453G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640339 | ||||||
| chr22:17640391
|
C | G | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+1505C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640391 | ||||||
| chr22:17640458
|
A | G | 1 | a0001c0001t0043g0001 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-51+1572A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640458 | ||||||
| chr22:17640592
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+1706G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640592 | ||||||
| chr22:17640701
|
T | TA | 45 | a0001c0001t0006g0070a0001c0001t0024g0243a0001c0001t0024g0244others(42): Show | 45 | HG00099.hp2 HG00423.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.-51+1829dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17640701 | |||||
| chr22:17640702
|
A | T | 21 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.-51+1816A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640702 | ||||||
| chr22:17640769
|
G | T | 1 | a0001c0001t0005g0218 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-51+1883G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640769 | ||||||
| chr22:17640775
|
G | A | 1 | a0001c0001t0065g0103 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-51+1889G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640775 | ||||||
| chr22:17640860
|
T | C | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-51+1974T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640860 | ||||||
| chr22:17640882
|
T | A | 1 | a0001c0001t0003g0021 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-51+1996T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640882 | ||||||
| chr22:17640882
|
T | TTA | 5 | a0001c0001t0002g0116a0001c0001t0004g0114a0001c0001t0004g0115others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+2012_-51+2013d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17640882 | |||||
| chr22:17640894
|
AT | A | 90 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-51+2009delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640894 | ||||||
| chr22:17640896
|
A | AT | 9 | a0001c0001t0002g0100a0001c0001t0002g0215a0001c0001t0002g0216others(6): Show | 9 | HG01192.hp1 HG02723.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+2011dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17640896 | |||||
| chr22:17640896
|
A | C | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+2010A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640896 | ||||||
| chr22:17640898
|
A | AT | 116 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0134others(113): Show | 116 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-51+2022dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17640898 | |||||
| chr22:17640898
|
A | T | 102 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0212others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.-51+2012A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640898 | ||||||
| chr22:17640899
|
T | TA | 28 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0003g0057others(25): Show | 28 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.-51+2013_-51+2014i others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640899 | ||||||
| chr22:17640900
|
T | A | 1 | a0002c0003t0001g0262 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-51+2014T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640900 | ||||||
| chr22:17640912
|
G | A | 19 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(16): Show | 19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-51+2026G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640912 | ||||||
| chr22:17640921
|
C | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+2035C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640921 | ||||||
| chr22:17641040
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+2154G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641040 | ||||||
| chr22:17641127
|
C | T | 1 | a0001c0002t0006g0079 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-51+2241C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641127 | ||||||
| chr22:17641362
|
G | T | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-51+2476G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641362 | ||||||
| chr22:17641387
|
A | AT | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51+2510dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17641387 | |||||
| chr22:17641406
|
C | T | 1 | a0001c0001t0008g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-51+2520C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641406 | ||||||
| chr22:17641566
|
G | A | 92 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-51+2680G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641566 | ||||||
| chr22:17641596
|
G | A | 92 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-51+2710G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641596 | ||||||
| chr22:17641740
|
TC | T | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+2855delC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641740 | ||||||
| chr22:17641798
|
G | GT | 19 | a0001c0001t0002g0100a0001c0001t0002g0203a0001c0001t0002g0204others(16): Show | 19 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.-51+2931dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17641798 | |||||
| chr22:17641798
|
GT | G | 49 | a0001c0001t0002g0126a0001c0001t0005g0007a0001c0001t0007g0008others(46): Show | 49 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-51+2931delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17641798 | |||||
| chr22:17641800
|
T | TG | 4 | a0001c0001t0003g0107a0001c0002t0006g0077a0001c0002t0006g0078others(1): Show | 4 | HG02071.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+2914_-51+2915i others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641800 | ||||||
| chr22:17641801
|
T | G | 60 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.-51+2915T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641801 | ||||||
| chr22:17641802
|
T | G | 23 | a0001c0001t0066g0011a0001c0002t0012g0003a0001c0002t0012g0004others(20): Show | 23 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.-51+2916T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641802 | ||||||
| chr22:17641803
|
T | G | 5 | a0004c0006t0001g0092a0004c0006t0049g0091a0004c0006t0063g0093others(2): Show | 5 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+2917T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641803 | ||||||
| chr22:17641834
|
C | T | 2 | a0001c0001t0008g0232a0001c0001t0020g0231 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-51+2948C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641834 | ||||||
| chr22:17641884
|
C | T | 1 | a0001c0001t0057g0125 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-51+2998C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641884 | ||||||
| chr22:17641893
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+3007G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641893 | ||||||
| chr22:17641901
|
G | A | 1 | a0001c0001t0003g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-51+3015G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641901 | ||||||
| chr22:17641989
|
CGGGGTTT others(1807): Show |
C | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-51+3114_-51+4927d others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17641989 | |||||
| chr22:17642129
|
CT | C | 197 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0116others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-51+3264delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17642129 | |||||
| chr22:17642129
|
CTTT | C | 44 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(41): Show | 44 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.-51+3262_-51+3264d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17642129 | |||||
| chr22:17642156
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-51+3270G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17642156 | ||||||
| chr22:17642189
|
G | A | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-51+3303G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17642189 | ||||||
| chr22:17642210
|
G | A | 14 | a0001c0002t0001g0247a0003c0004t0015g0080a0003c0004t0015g0081others(11): Show | 14 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.-51+3324G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17642210 | ||||||
| chr22:17642216
|
C | G | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-51+3330C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17642216 | ||||||
| chr22:17642334
|
T | C | 1 | a0001c0001t0055g0129 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-51+3448T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17642334 | ||||||
| chr22:17642597
|
A | AT | 28 | a0001c0001t0002g0211a0001c0001t0004g0202a0001c0001t0004g0246others(25): Show | 28 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.-51+3724dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17642597 | |||||
| chr22:17642697
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+3811G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17642697 | ||||||
| chr22:17643031
|
C | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-51+4145C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643031 | ||||||
| chr22:17643254
|
T | C | 157 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0116others(154): Show | 157 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.-51+4368T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643254 | ||||||
| chr22:17643276
|
A | G | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+4390A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643276 | ||||||
| chr22:17643396
|
G | A | 72 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-51+4510G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643396 | ||||||
| chr22:17643422
|
G | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-51+4536G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643422 | ||||||
| chr22:17643466
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+4580G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643466 | ||||||
| chr22:17643507
|
T | C | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+4621T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643507 | ||||||
| chr22:17643536
|
C | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+4650C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643536 | ||||||
| chr22:17643684
|
G | C | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+4798G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643684 | ||||||
| chr22:17643749
|
G | T | 3 | a0001c0007t0009g0053a0001c0007t0009g0056a0001c0007t0044g0052 | 3 | HG03130.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-51+4863G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643749 | ||||||
| chr22:17643763
|
G | A | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+4877G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643763 | ||||||
| chr22:17643787
|
G | A | 1 | a0001c0002t0026g0299 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-51+4901G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643787 | ||||||
| chr22:17643801
|
G | A | 1 | a0001c0001t0004g0097 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-51+4915G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643801 | ||||||
| chr22:17643860
|
T | A | 2 | a0001c0001t0007g0008a0001c0001t0007g0009 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-51+4974T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643860 | ||||||
| chr22:17643888
|
C | T | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5002C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643888 | ||||||
| chr22:17643897
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5011G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643897 | ||||||
| chr22:17643902
|
G | C | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5016G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643902 | ||||||
| chr22:17643903
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5017G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643903 | ||||||
| chr22:17643909
|
G | A | 1 | a0001c0001t0004g0130 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-51+5023G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643909 | ||||||
| chr22:17643913
|
A | T | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5027A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643913 | ||||||
| chr22:17643915
|
CTTTTTTA others(1985): Show |
C | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5030_-51+7021d others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643915 | ||||||
| chr22:17643977
|
C | T | 19 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(16): Show | 19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-51+5091C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643977 | ||||||
| chr22:17644062
|
C | T | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-51+5176C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644062 | ||||||
| chr22:17644112
|
T | C | 1 | a0001c0002t0006g0079 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-51+5226T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644112 | ||||||
| chr22:17644130
|
C | T | 3 | a0003c0004t0016g0087a0003c0004t0016g0088a0003c0004t0016g0089 | 3 | HG01934.hp2 HG02055.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-51+5244C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644130 | ||||||
| chr22:17644169
|
C | A | 1 | a0001c0001t0002g0203 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-51+5283C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644169 | ||||||
| chr22:17644306
|
C | G | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-51+5420C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644306 | ||||||
| chr22:17644310
|
G | A | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51+5424G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644310 | ||||||
| chr22:17644334
|
C | CT | 24 | a0001c0001t0004g0098a0001c0001t0004g0200a0001c0001t0004g0201others(21): Show | 24 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.-51+5463dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17644334 | |||||
| chr22:17644334
|
CT | C | 8 | a0001c0001t0002g0100a0001c0001t0002g0204a0001c0001t0003g0022others(5): Show | 8 | HG02040.hp1 HG02135.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.-51+5463delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17644334 | |||||
| chr22:17644534
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+5648G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644534 | ||||||
| chr22:17644558
|
T | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-51+5672T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644558 | ||||||
| chr22:17644574
|
C | T | 1 | a0006c0010t0001g0263 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-51+5688C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644574 | ||||||
| chr22:17644610
|
A | G | 3 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0204 | 3 | HG03927.hp1 HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-51+5724A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644610 | ||||||
| chr22:17644671
|
G | A | 87 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-51+5785G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644671 | ||||||
| chr22:17644811
|
T | C | 2 | a0001c0002t0001g0264a0001c0002t0001g0265 | 2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-51+5925T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644811 | ||||||
| chr22:17644959
|
G | A | 19 | a0002c0003t0001g0220a0002c0003t0001g0221a0002c0003t0001g0262others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-51+6073G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644959 | ||||||
| chr22:17645130
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+6244G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17645130 | ||||||
| chr22:17645225
|
A | AT | 6 | a0001c0001t0028g0303a0001c0002t0001g0265a0001c0002t0001g0291others(3): Show | 6 | HG00408.hp2 HG02572.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51+6360dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17645225 | |||||
| chr22:17645225
|
AT | A | 162 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0116others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-51+6360delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17645225 | |||||
| chr22:17645225
|
ATT | A | 61 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0003g0002others(58): Show | 61 | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.-51+6359_-51+6360d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17645225 | |||||
| chr22:17645315
|
C | T | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51+6429C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17645315 | ||||||
| chr22:17645895
|
C | T | 1 | a0001c0002t0001g0290 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-51+7009C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17645895 | ||||||
| chr22:17645914
|
AATACAAA others(810): Show |
A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+7029_-51+7845d others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17645914 | ||||||
| chr22:17646117
|
A | G | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-51+7231A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646117 | ||||||
| chr22:17646194
|
G | A | 248 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.-51+7308G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646194 | ||||||
| chr22:17646227
|
G | A | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+7341G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646227 | ||||||
| chr22:17646247
|
T | A | 1 | a0001c0001t0036g0094 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-51+7361T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646247 | ||||||
| chr22:17646309
|
C | T | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-51+7423C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646309 | ||||||
| chr22:17646369
|
C | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+7483C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646369 | ||||||
| chr22:17646438
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-51+7552G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646438 | ||||||
| chr22:17646494
|
C | T | 2 | a0001c0001t0005g0059a0001c0001t0005g0060 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51+7608C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646494 | ||||||
| chr22:17646499
|
G | T | 248 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.-51+7613G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646499 | ||||||
| chr22:17646525
|
A | G | 2 | a0001c0001t0002g0295a0001c0001t0002g0296 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-51+7639A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646525 | ||||||
| chr22:17646558
|
A | G | 2 | a0001c0002t0025g0074a0001c0002t0025g0075 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-51+7672A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646558 | ||||||
| chr22:17646581
|
TG | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-51+7696delG | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646581 | ||||||
| chr22:17646598
|
G | T | 19 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(16): Show | 19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-51+7712G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646598 | ||||||
| chr22:17646599
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+7713G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646599 | ||||||
| chr22:17646714
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+7828G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646714 | ||||||
| chr22:17646716
|
C | CTT | 13 | a0001c0001t0002g0111a0001c0001t0002g0128a0001c0001t0003g0024others(10): Show | 13 | HG00099.hp2 HG00323.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+7850_-51+7851d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646716 | |||||
| chr22:17646716
|
C | CTTT | 156 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0112others(153): Show | 156 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.-51+7849_-51+7851d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646716 | |||||
| chr22:17646716
|
C | CTTTT | 58 | a0001c0001t0002g0189a0001c0001t0002g0194a0001c0001t0002g0195others(55): Show | 58 | HG00140.hp2 HG00733.hp1 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.-51+7848_-51+7851d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646716 | |||||
| chr22:17646716
|
C | CTTTTT | 6 | a0001c0001t0003g0051a0001c0001t0003g0107a0001c0001t0007g0012others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+7847_-51+7851d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646716 | |||||
| chr22:17646733
|
T | C | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+7847T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646733 | ||||||
| chr22:17646885
|
A | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+7999A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646885 | ||||||
| chr22:17646888
|
T | TTG | 3 | a0001c0002t0035g0301a0002c0003t0001g0279a0002c0003t0001g0280 | 3 | HG01069.hp2 HG01071.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-51+8036_-51+8037d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646888 | |||||
| chr22:17646888
|
TTG | T | 11 | a0001c0001t0003g0021a0001c0001t0003g0048a0001c0001t0003g0049others(8): Show | 11 | HG01256.hp2 HG02280.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.-51+8036_-51+8037d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646888 | |||||
| chr22:17646888
|
TTGTG | T | 56 | a0001c0001t0003g0022a0001c0001t0003g0034a0001c0001t0003g0035others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.-51+8034_-51+8037d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646888 | |||||
| chr22:17646888
|
TTGTGTG | T | 174 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0126others(171): Show | 174 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.-51+8032_-51+8037d others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646888 | |||||
| chr22:17646888
|
TTGTGTGT others(3): Show |
T | 9 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0116others(6): Show | 9 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51+8028_-51+8037d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646888 | |||||
| chr22:17646922
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+8036G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646922 | ||||||
| chr22:17646932
|
C | CATATAT | 7 | a0001c0001t0002g0144a0001c0001t0002g0189a0001c0001t0002g0199others(4): Show | 7 | HG01496.hp1 HG01934.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51+8065_-51+8070d others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646932 | |||||
| chr22:17646948
|
TA | T | 3 | a0004c0006t0001g0092a0004c0006t0049g0091a0004c0006t0063g0093 | 3 | HG02280.hp2 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-51+8063delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646948 | ||||||
| chr22:17646951
|
A | T | 7 | a0001c0002t0012g0004a0001c0002t0026g0300a0001c0002t0035g0301others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51+8065A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646951 | ||||||
| chr22:17646951
|
ATATAT | A | 21 | a0001c0001t0003g0021a0001c0001t0003g0039a0001c0001t0003g0041others(18): Show | 21 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51+8067_-51+8071d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646951 | |||||
| chr22:17646953
|
A | AT | 3 | a0001c0001t0008g0230a0001c0001t0066g0011a0001c0002t0069g0294 | 3 | HG00408.hp2 HG02109.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.-51+8068dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646953 | |||||
| chr22:17646953
|
A | T | 18 | a0001c0001t0038g0228a0001c0002t0001g0095a0001c0002t0001g0261others(15): Show | 18 | HG01884.hp1 HG01981.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-51+8067A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646953 | ||||||
| chr22:17646953
|
ATATTTTT others(1): Show |
A | 10 | a0001c0001t0003g0024a0001c0001t0003g0027a0001c0001t0003g0029others(7): Show | 10 | HG02572.hp2 HG02630.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-51+8069_-51+8076d others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646953 | |||||
| chr22:17646953
|
ATATTTTT others(4): Show |
A | 1 | a0001c0001t0007g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-51+8069_-51+8079d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646953 | |||||
| chr22:17646954
|
TA | T | 7 | a0001c0002t0001g0260a0001c0002t0001g0264a0001c0002t0001g0265others(4): Show | 7 | HG00639.hp2 HG02486.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51+8069delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646954 | ||||||
| chr22:17646955
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0005g0142a0001c0001t0005g0143 | 2 | HG03540.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0005g0197a0001c0001t0055g0129 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0005g0218 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-51+8070_-51+8071i others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATATAT others(5): Show |
2 | a0001c0001t0002g0295a0001c0001t0005g0145 | 2 | HG01109.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0296 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-51+8070_-51+8071i others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0002g0147a0001c0001t0005g0148 | 2 | HG02071.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATATAT others(4): Show |
4 | a0001c0001t0002g0150a0001c0001t0004g0201a0001c0001t0005g0149others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0005g0190 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-51+8070_-51+8071i others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0004g0191 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-51+8070_-51+8071i others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATATT | 15 | a0001c0001t0002g0116a0001c0001t0002g0215a0001c0001t0004g0097others(12): Show | 15 | HG00423.hp2 HG00438.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATATTT | 9 | a0001c0001t0002g0100a0001c0001t0002g0126a0001c0001t0002g0138others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(9): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATATTT others(1): Show |
9 | a0001c0001t0002g0156a0001c0001t0002g0212a0001c0001t0004g0098others(6): Show | 9 | HG00544.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATATTT others(2): Show |
10 | a0001c0001t0002g0128a0001c0001t0002g0162a0001c0001t0004g0163others(7): Show | 10 | HG00323.hp1 HG00408.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(11): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATATTT others(3): Show |
2 | a0001c0001t0002g0194a0001c0001t0032g0166 | 2 | HG02004.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATTTT | 9 | a0001c0001t0002g0134a0001c0001t0002g0168a0001c0001t0002g0169others(6): Show | 9 | HG01081.hp2 HG01167.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | ATATTTTT | 15 | a0001c0001t0002g0141a0001c0001t0002g0172a0001c0001t0002g0175others(12): Show | 15 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(9): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
A | T | 50 | a0001c0001t0008g0229a0001c0001t0008g0230a0001c0001t0036g0094others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.-51+8069A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646955 | ||||||
| chr22:17646955
|
ATTTT | A | 10 | a0001c0002t0006g0068a0001c0002t0006g0069a0001c0002t0006g0077others(7): Show | 10 | HG00099.hp2 HG01175.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-51+8090_-51+8093d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
ATTTTT | A | 13 | a0001c0001t0007g0017a0001c0002t0006g0067a0001c0002t0025g0074others(10): Show | 13 | HG00423.hp1 HG01109.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+8089_-51+8093d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646955
|
ATTTTTTT | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0009a0001c0001t0007g0012others(9): Show | 12 | HG00738.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+8087_-51+8093d others(9): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | |||||
| chr22:17646956
|
T | TA | 3 | a0001c0002t0001g0120a0002c0003t0001g0266a0002c0003t0001g0267 | 3 | HG01168.hp1 HG01169.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646956 | ||||||
| chr22:17646957
|
T | A | 3 | a0001c0001t0002g0144a0005c0008t0019g0255a0005c0008t0019g0256 | 3 | HG01496.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+8071T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646957 | ||||||
| chr22:17646958
|
T | A | 1 | a0001c0002t0037g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-51+8072T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646958 | ||||||
| chr22:17646959
|
T | A | 3 | a0001c0001t0007g0108a0005c0008t0019g0255a0005c0008t0019g0256 | 3 | HG02965.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+8073T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646959 | ||||||
| chr22:17646960
|
T | A | 2 | a0001c0002t0006g0079a0001c0002t0037g0062 | 2 | NA19030.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-51+8074T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646960 | ||||||
| chr22:17646961
|
T | A | 5 | a0001c0001t0007g0108a0003c0004t0016g0089a0003c0004t0030g0101others(2): Show | 5 | HG01175.hp2 HG02055.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+8075T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646961 | ||||||
| chr22:17646962
|
T | A | 10 | a0001c0001t0007g0017a0001c0002t0025g0074a0001c0002t0025g0075others(7): Show | 10 | HG01109.hp2 HG01361.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51+8076T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646962 | ||||||
| chr22:17646963
|
T | A | 6 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0118others(3): Show | 6 | HG01175.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+8077T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646963 | ||||||
| chr22:17646964
|
T | A | 13 | a0001c0001t0007g0008a0001c0001t0007g0009a0001c0001t0007g0012others(10): Show | 13 | HG01934.hp2 HG02148.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51+8078T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646964 | ||||||
| chr22:17646965
|
T | A | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0118 | 3 | HG03195.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-51+8079T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646965 | ||||||
| chr22:17646966
|
T | A | 3 | a0001c0001t0007g0008a0001c0001t0007g0009a0003c0004t0015g0080 | 3 | HG02148.hp2 HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-51+8080T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646966 | ||||||
| chr22:17646971
|
T | C | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+8085T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646971 | ||||||
| chr22:17647004
|
T | C | 92 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-51+8118T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647004 | ||||||
| chr22:17647067
|
G | A | 1 | a0001c0001t0009g0038 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-51+8181G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647067 | ||||||
| chr22:17647176
|
G | A | 19 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(16): Show | 19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-51+8290G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647176 | ||||||
| chr22:17647372
|
T | G | 27 | a0001c0001t0006g0070a0001c0001t0066g0011a0001c0002t0006g0066others(24): Show | 27 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.-50-8290T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647372 | ||||||
| chr22:17647403
|
G | A | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-8259G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647403 | ||||||
| chr22:17647441
|
C | T | 1 | a0001c0001t0018g0171 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-50-8221C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647441 | ||||||
| chr22:17647443
|
C | T | 12 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(9): Show | 12 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50-8219C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647443 | ||||||
| chr22:17647451
|
A | G | 1 | a0001c0002t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-50-8211A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647451 | ||||||
| chr22:17647749
|
A | G | 4 | a0001c0001t0006g0070a0001c0002t0006g0071a0001c0002t0006g0072others(1): Show | 4 | HG02145.hp1 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50-7913A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647749 | ||||||
| chr22:17647801
|
C | T | 1 | a0004c0006t0001g0092 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-50-7861C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647801 | ||||||
| chr22:17647854
|
C | T | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-7808C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647854 | ||||||
| chr22:17647855
|
G | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-50-7807G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647855 | ||||||
| chr22:17647954
|
C | T | 1 | a0001c0001t0005g0241 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-50-7708C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647954 | ||||||
| chr22:17648033
|
G | C | 1 | a0001c0001t0002g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-50-7629G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648033 | ||||||
| chr22:17648103
|
C | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-7559C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648103 | ||||||
| chr22:17648106
|
C | T | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-7556C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648106 | ||||||
| chr22:17648132
|
A | G | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-7530A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648132 | ||||||
| chr22:17648166
|
T | C | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-7496T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648166 | ||||||
| chr22:17648231
|
C | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-50-7431C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648231 | ||||||
| chr22:17648312
|
C | T | 257 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.-50-7350C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648312 | ||||||
| chr22:17648318
|
A | C | 8 | a0001c0001t0003g0022a0001c0001t0003g0035a0001c0001t0003g0036others(5): Show | 8 | HG02135.hp2 NA18968.hp2 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50-7344A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648318 | ||||||
| chr22:17648388
|
T | A | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-7274T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648388 | ||||||
| chr22:17648435
|
C | T | 1 | a0001c0001t0002g0126 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-50-7227C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648435 | ||||||
| chr22:17648460
|
C | T | 161 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-50-7202C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648460 | ||||||
| chr22:17648526
|
C | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-7136C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648526 | ||||||
| chr22:17648603
|
C | A | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-50-7059C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648603 | ||||||
| chr22:17648657
|
A | T | 3 | a0001c0001t0018g0206a0001c0001t0018g0207a0001c0001t0039g0160 | 3 | HG00438.hp2 HG00544.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.-50-7005A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648657 | ||||||
| chr22:17648665
|
T | C | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-6997T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648665 | ||||||
| chr22:17648780
|
A | G | 159 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(156): Show | 159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.-50-6882A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648780 | ||||||
| chr22:17648830
|
T | C | 1 | a0001c0001t0065g0103 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-50-6832T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648830 | ||||||
| chr22:17648933
|
A | AT | 22 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-6720dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17648933 | |||||
| chr22:17649010
|
A | T | 4 | a0001c0001t0002g0116a0001c0001t0002g0138a0001c0001t0002g0188others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-6652A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649010 | ||||||
| chr22:17649011
|
C | T | 4 | a0001c0001t0002g0116a0001c0001t0002g0138a0001c0001t0002g0188others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-6651C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649011 | ||||||
| chr22:17649094
|
C | T | 2 | a0001c0002t0035g0301a0005c0008t0019g0298 | 2 | HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-50-6568C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649094 | ||||||
| chr22:17649101
|
A | AT | 6 | a0001c0001t0002g0186a0001c0001t0005g0060a0001c0001t0013g0165others(3): Show | 6 | HG00099.hp1 HG01255.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-6547dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17649101 | |||||
| chr22:17649189
|
C | T | 2 | a0001c0001t0022g0237a0001c0001t0022g0239 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-50-6473C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649189 | ||||||
| chr22:17649231
|
G | A | 1 | a0001c0002t0006g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-50-6431G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649231 | ||||||
| chr22:17649238
|
T | C | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-50-6424T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649238 | ||||||
| chr22:17649348
|
C | T | 1 | a0001c0001t0038g0228 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-50-6314C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649348 | ||||||
| chr22:17649472
|
T | C | 1 | a0001c0001t0003g0002 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-50-6190T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649472 | ||||||
| chr22:17649526
|
G | A | 1 | a0001c0002t0001g0290 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-50-6136G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649526 | ||||||
| chr22:17649871
|
C | CTTT | 20 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(17): Show | 20 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.-50-5775_-50-5773d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17649871 | |||||
| chr22:17649871
|
CT | C | 212 | a0001c0001t0002g0100a0001c0001t0002g0111a0001c0001t0002g0112others(209): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.-50-5773delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17649871 | |||||
| chr22:17649871
|
CTT | C | 12 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0003g0048others(9): Show | 12 | HG01069.hp1 HG01109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-50-5774_-50-5773d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17649871 | |||||
| chr22:17649874
|
T | TC | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50-5788_-50-5787i others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649874 | ||||||
| chr22:17649877
|
T | C | 2 | a0001c0001t0007g0008a0001c0001t0007g0009 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-50-5785T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649877 | ||||||
| chr22:17649993
|
C | T | 1 | a0001c0001t0004g0131 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-50-5669C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649993 | ||||||
| chr22:17650016
|
G | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-50-5646G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650016 | ||||||
| chr22:17650046
|
G | T | 180 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(177): Show | 180 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.-50-5616G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650046 | ||||||
| chr22:17650056
|
G | A | 1 | a0001c0002t0001g0119 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-50-5606G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650056 | ||||||
| chr22:17650162
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-5500G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650162 | ||||||
| chr22:17650164
|
C | T | 161 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-50-5498C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650164 | ||||||
| chr22:17650394
|
A | G | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-5268A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650394 | ||||||
| chr22:17650443
|
T | C | 1 | a0001c0001t0064g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-50-5219T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650443 | ||||||
| chr22:17650469
|
C | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-5193C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650469 | ||||||
| chr22:17650724
|
A | T | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.-50-4938A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650724 | ||||||
| chr22:17650734
|
A | C | 161 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-50-4928A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650734 | ||||||
| chr22:17650828
|
C | T | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-50-4834C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650828 | ||||||
| chr22:17650964
|
C | T | 2 | a0001c0001t0003g0046a0001c0001t0003g0047 | 2 | NA18967.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-50-4698C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650964 | ||||||
| chr22:17650975
|
C | T | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-4687C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650975 | ||||||
| chr22:17650979
|
G | A | 1 | a0001c0001t0007g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-50-4683G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650979 | ||||||
| chr22:17650991
|
C | CT | 153 | a0001c0001t0002g0099a0001c0001t0002g0111a0001c0001t0002g0112others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.-50-4651dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17650991 | |||||
| chr22:17650991
|
C | CTT | 28 | a0001c0001t0002g0100a0001c0001t0002g0198a0001c0001t0005g0059others(25): Show | 28 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.-50-4652_-50-4651d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17650991 | |||||
| chr22:17651042
|
G | A | 135 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.-50-4620G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651042 | ||||||
| chr22:17651367
|
C | CTATT | 19 | a0001c0001t0006g0070a0001c0002t0001g0287a0001c0002t0006g0066others(16): Show | 19 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.-50-4265_-50-4262d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17651367 | |||||
| chr22:17651367
|
CTATT | C | 230 | a0001c0001t0002g0099a0001c0001t0002g0111a0001c0001t0002g0112others(227): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-50-4265_-50-4262d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17651367 | |||||
| chr22:17651389
|
A | T | 1 | a0001c0001t0013g0236 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-50-4273A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651389 | ||||||
| chr22:17651393
|
A | T | 22 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-4269A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651393 | ||||||
| chr22:17651397
|
A | T | 179 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(176): Show | 179 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-50-4265A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651397 | ||||||
| chr22:17651474
|
C | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-4188C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651474 | ||||||
| chr22:17651499
|
C | T | 159 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(156): Show | 159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.-50-4163C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651499 | ||||||
| chr22:17651705
|
T | G | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-3957T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651705 | ||||||
| chr22:17651719
|
C | G | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-3943C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651719 | ||||||
| chr22:17651721
|
C | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-3941C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651721 | ||||||
| chr22:17651722
|
A | G | 19 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(16): Show | 19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50-3940A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651722 | ||||||
| chr22:17651729
|
C | T | 1 | a0001c0001t0004g0208 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-50-3933C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651729 | ||||||
| chr22:17651730
|
G | A | 1 | a0001c0001t0018g0171 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-50-3932G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651730 | ||||||
| chr22:17651845
|
C | T | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-50-3817C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651845 | ||||||
| chr22:17651946
|
T | C | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-50-3716T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651946 | ||||||
| chr22:17652084
|
T | C | 248 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.-50-3578T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652084 | ||||||
| chr22:17652090
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-3572G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652090 | ||||||
| chr22:17652127
|
T | C | 8 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0118others(5): Show | 8 | HG01255.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50-3535T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652127 | ||||||
| chr22:17652162
|
ACATAGCT others(4): Show |
A | 1 | a0001c0002t0027g0006 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-50-3498_-50-3488d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17652162 | |||||
| chr22:17652210
|
A | T | 180 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(177): Show | 180 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.-50-3452A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652210 | ||||||
| chr22:17652235
|
G | A | 45 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(42): Show | 45 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.-50-3427G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652235 | ||||||
| chr22:17652243
|
G | A | 1 | a0002c0003t0001g0268 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-50-3419G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652243 | ||||||
| chr22:17652418
|
T | C | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-3244T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652418 | ||||||
| chr22:17652442
|
A | G | 4 | a0001c0002t0014g0061a0001c0002t0014g0063a0001c0002t0014g0064others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50-3220A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652442 | ||||||
| chr22:17652508
|
G | A | 1 | a0001c0001t0051g0205 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-50-3154G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652508 | ||||||
| chr22:17652978
|
T | A | 1 | a0001c0001t0005g0142 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-50-2684T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652978 | ||||||
| chr22:17653019
|
C | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-2643C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653019 | ||||||
| chr22:17653146
|
A | G | 92 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-50-2516A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653146 | ||||||
| chr22:17653234
|
A | G | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-2428A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653234 | ||||||
| chr22:17653267
|
T | C | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-2395T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653267 | ||||||
| chr22:17653451
|
T | C | 1 | a0001c0001t0002g0213 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-50-2211T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653451 | ||||||
| chr22:17653495
|
A | AT | 14 | a0001c0001t0002g0150a0001c0001t0002g0186a0001c0001t0002g0188others(11): Show | 14 | HG00099.hp1 HG00280.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.-50-2145dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653495 | |||||
| chr22:17653495
|
A | ATT | 40 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0025others(37): Show | 40 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.-50-2146_-50-2145d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653495 | |||||
| chr22:17653495
|
A | ATTT | 7 | a0001c0001t0002g0100a0001c0001t0003g0021a0001c0001t0003g0024others(4): Show | 7 | HG02647.hp2 HG06807.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-2147_-50-2145d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653495 | |||||
| chr22:17653495
|
AT | A | 40 | a0001c0001t0006g0070a0001c0001t0007g0096a0001c0001t0008g0229others(37): Show | 40 | HG00099.hp2 HG00738.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.-50-2145delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653495 | |||||
| chr22:17653495
|
ATT | A | 16 | a0001c0001t0024g0243a0001c0001t0024g0244a0001c0002t0014g0063others(13): Show | 16 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50-2146_-50-2145d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653495 | |||||
| chr22:17653769
|
G | T | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-50-1893G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653769 | ||||||
| chr22:17653808
|
T | C | 2 | a0001c0001t0005g0145a0001c0001t0005g0197 | 2 | HG01109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-50-1854T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653808 | ||||||
| chr22:17653856
|
T | TAAAAATT others(1708): Show |
1 | a0001c0001t0003g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1717): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1709): Show |
1 | a0001c0001t0003g0002 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1718): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1707): Show |
1 | a0001c0001t0009g0033 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1716): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1705): Show |
1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1714): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1706): Show |
1 | a0001c0001t0003g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1715): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1707): Show |
1 | a0001c0001t0043g0001 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1716): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1707): Show |
1 | a0001c0001t0023g0105 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1716): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1708): Show |
1 | a0001c0001t0003g0021 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1717): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1706): Show |
1 | a0001c0001t0003g0049 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1715): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1703): Show |
1 | a0001c0001t0003g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1712): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1704): Show |
2 | a0001c0001t0003g0031a0001c0001t0003g0058 | 2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1713): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1705): Show |
7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0029others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1714): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1705): Show |
10 | a0001c0001t0003g0034a0001c0001t0003g0041a0001c0001t0003g0042others(7): Show | 10 | HG04199.hp1 NA18955.hp1 NA18974.hp1 others(7): Show |
intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1714): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1706): Show |
12 | a0001c0001t0003g0022a0001c0001t0003g0035a0001c0001t0003g0037others(9): Show | 12 | HG00733.hp1 HG01168.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1715): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1578): Show |
1 | a0001c0001t0046g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1587): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1706): Show |
1 | a0001c0007t0009g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1715): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1707): Show |
1 | a0001c0001t0003g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1716): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653856
|
T | TAAAAATT others(1707): Show |
2 | a0001c0001t0003g0045a0001c0001t0003g0054 | 2 | NA18989.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1716): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | |||||
| chr22:17653929
|
C | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-1733C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653929 | ||||||
| chr22:17653976
|
T | C | 2 | a0001c0001t0005g0059a0001c0001t0005g0060 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-50-1686T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653976 | ||||||
| chr22:17653992
|
C | A | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-1670C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653992 | ||||||
| chr22:17654008
|
T | G | 1 | a0005c0008t0019g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-50-1654T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654008 | ||||||
| chr22:17654037
|
A | G | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-1625A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654037 | ||||||
| chr22:17654223
|
A | G | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-1439A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654223 | ||||||
| chr22:17654308
|
T | TA | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-1353dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17654308 | |||||
| chr22:17654378
|
T | C | 252 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.-50-1284T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654378 | ||||||
| chr22:17654397
|
C | T | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-50-1265C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654397 | ||||||
| chr22:17654461
|
C | T | 3 | a0001c0001t0008g0226a0001c0001t0024g0243a0001c0001t0024g0244 | 3 | HG02895.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-50-1201C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654461 | ||||||
| chr22:17654508
|
C | T | 161 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-50-1154C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654508 | ||||||
| chr22:17654584
|
G | A | 2 | a0001c0002t0012g0305a0001c0002t0012g0306 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-50-1078G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654584 | ||||||
| chr22:17654589
|
A | T | 1 | a0001c0001t0002g0203 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-50-1073A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654589 | ||||||
| chr22:17654857
|
G | T | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50-805G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654857 | ||||||
| chr22:17655022
|
C | T | 2 | a0001c0001t0002g0295a0001c0001t0002g0296 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-50-640C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17655022 | ||||||
| chr22:17655065
|
CT | C | 252 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.-50-587delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17655065 | |||||
| chr22:17655108
|
A | T | 1 | a0001c0001t0056g0214 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-50-554A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17655108 | ||||||
| chr22:17655300
|
C | CT | 12 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(9): Show | 12 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50-347dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17655300 | |||||
| chr22:17655300
|
CT | C | 11 | a0001c0001t0002g0216a0001c0001t0003g0039a0001c0001t0004g0131others(8): Show | 11 | HG02280.hp2 HG02886.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.-50-347delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17655300 | |||||
| chr22:17655425
|
CT | C | 7 | a0001c0001t0006g0070a0001c0001t0007g0248a0001c0001t0007g0249others(4): Show | 7 | HG01168.hp2 HG02145.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-223delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17655425 | |||||
| chr22:17655480
|
A | G | 22 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-182A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17655480 | ||||||
| chr22:17655960
|
G | C | 5 | a0002c0003t0001g0269a0002c0003t0001g0271a0002c0003t0001g0272others(2): Show | 5 | HG00280.hp2 HG01123.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+128G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17655960 | ||||||
| chr22:17656025
|
G | A | 4 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0118others(1): Show | 4 | HG02896.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+193G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656025 | ||||||
| chr22:17656091
|
A | G | 1 | a0001c0001t0043g0001 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.121+259A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656091 | ||||||
| chr22:17656113
|
C | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+281C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656113 | ||||||
| chr22:17656154
|
C | T | 1 | a0001c0001t0005g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.121+322C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656154 | ||||||
| chr22:17656165
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+333G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656165 | ||||||
| chr22:17656232
|
T | A | 73 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.121+400T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656232 | ||||||
| chr22:17656239
|
C | CA | 166 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(163): Show | 166 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.121+420dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656239 | |||||
| chr22:17656251
|
A | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+419A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656251 | ||||||
| chr22:17656253
|
T | A | 1 | a0001c0001t0002g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.121+421T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656253 | ||||||
| chr22:17656304
|
A | C | 1 | a0001c0001t0002g0128 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.121+472A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656304 | ||||||
| chr22:17656312
|
A | G | 1 | a0001c0001t0007g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.121+480A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656312 | ||||||
| chr22:17656335
|
C | CT | 55 | a0001c0001t0002g0116a0001c0001t0002g0128a0001c0001t0002g0134others(52): Show | 55 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.121+536dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
C | CTT | 33 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0126others(30): Show | 33 | HG00544.hp1 HG00639.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.121+535_121+536dup others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
C | CTTTT | 20 | a0001c0001t0002g0203a0001c0001t0003g0022a0001c0001t0003g0034others(17): Show | 20 | HG00140.hp2 HG01168.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.121+533_121+536dup others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
C | CTTTTT | 13 | a0001c0001t0003g0021a0001c0001t0003g0036a0001c0001t0003g0044others(10): Show | 13 | HG00733.hp1 HG01496.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+532_121+536dup others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
CT | C | 15 | a0001c0001t0003g0252a0001c0001t0005g0007a0001c0001t0010g0238others(12): Show | 15 | HG00639.hp2 HG00741.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.121+536delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
CTT | C | 9 | a0001c0001t0003g0251a0001c0001t0008g0223a0001c0001t0008g0227others(6): Show | 9 | HG01433.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+535_121+536del others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
CTTT | C | 15 | a0001c0001t0008g0222a0001c0001t0008g0230a0001c0001t0008g0232others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.121+534_121+536del others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
CTTTTTTT | C | 7 | a0001c0001t0002g0172a0001c0001t0046g0023a0002c0003t0001g0276others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.121+530_121+536del others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
CTTTTTTT others(1): Show |
C | 14 | a0002c0003t0001g0220a0002c0003t0001g0221a0002c0003t0001g0262others(11): Show | 14 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.121+529_121+536del others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0002t0006g0077a0001c0002t0014g0065a0001c0002t0027g0076 | 3 | HG02071.hp1 HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.121+527_121+536del others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
CTTTTTTT others(4): Show |
C | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.121+526_121+536del others(11): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
CTTTTTTT others(5): Show |
C | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+525_121+536del others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0004g0098a0003c0004t0016g0087a0003c0004t0030g0101 | 3 | HG01175.hp2 HG01934.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.121+524_121+536del others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
CTTTTTTT others(7): Show |
C | 10 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0016g0088others(7): Show | 10 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+523_121+536del others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
CTTTTTTT others(8): Show |
C | 1 | a0003c0004t0015g0253 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.121+522_121+536del others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
CTTTTTTT others(10): Show |
C | 5 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0118others(2): Show | 5 | HG02683.hp2 HG02896.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+520_121+536del others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656335
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0004g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.121+518_121+536del others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | |||||
| chr22:17656444
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.121+612C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656444 | ||||||
| chr22:17656445
|
G | A | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+613G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656445 | ||||||
| chr22:17656582
|
A | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+750A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656582 | ||||||
| chr22:17656636
|
G | T | 92 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.121+804G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656636 | ||||||
| chr22:17656744
|
A | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+912A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656744 | ||||||
| chr22:17656825
|
C | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+993C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656825 | ||||||
| chr22:17656855
|
G | C | 2 | a0001c0001t0002g0295a0001c0001t0002g0296 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.121+1023G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656855 | ||||||
| chr22:17656911
|
C | T | 1 | a0001c0001t0018g0206 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.121+1079C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656911 | ||||||
| chr22:17656923
|
A | G | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121+1091A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656923 | ||||||
| chr22:17656976
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.121+1144G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656976 | ||||||
| chr22:17656979
|
C | T | 1 | a0001c0002t0001g0281 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.121+1147C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656979 | ||||||
| chr22:17657368
|
TACTTA | T | 135 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.121+1540_121+1544d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657368 | |||||
| chr22:17657423
|
C | T | 1 | a0001c0001t0011g0167 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.121+1591C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657423 | ||||||
| chr22:17657521
|
C | CT | 7 | a0001c0001t0002g0150a0004c0006t0001g0090a0004c0006t0001g0092others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.121+1701dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657521 | |||||
| chr22:17657541
|
A | T | 1 | a0001c0002t0006g0072 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.121+1709A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657541 | ||||||
| chr22:17657575
|
C | T | 1 | a0001c0002t0006g0067 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.121+1743C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657575 | ||||||
| chr22:17657576
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+1744G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657576 | ||||||
| chr22:17657657
|
A | G | 92 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.121+1825A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657657 | ||||||
| chr22:17657664
|
A | T | 1 | a0001c0001t0002g0215 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.121+1832A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657664 | ||||||
| chr22:17657810
|
C | G | 1 | a0001c0001t0002g0215 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.121+1978C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657810 | ||||||
| chr22:17657823
|
C | CT | 23 | a0001c0001t0020g0224a0001c0001t0020g0233a0001c0001t0036g0094others(20): Show | 23 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.121+2012dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657823 | |||||
| chr22:17657823
|
C | CTT | 22 | a0001c0001t0008g0222a0001c0001t0008g0227a0001c0001t0008g0229others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.121+2011_121+2012d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657823 | |||||
| chr22:17657823
|
C | CTTTTTT | 117 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.121+2007_121+2012d others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657823 | |||||
| chr22:17657823
|
C | CTTTTTTT | 13 | a0001c0001t0002g0116a0001c0001t0002g0189a0001c0001t0002g0204others(10): Show | 13 | HG00544.hp1 HG01109.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+2006_121+2012d others(9): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657823 | |||||
| chr22:17657823
|
CTTTT | C | 69 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(66): Show | 69 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.121+2009_121+2012d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657823 | |||||
| chr22:17657854
|
C | G | 1 | a0001c0001t0002g0215 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.121+2022C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657854 | ||||||
| chr22:17657878
|
T | G | 92 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.121+2046T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657878 | ||||||
| chr22:17657967
|
C | T | 2 | a0001c0001t0005g0007a0001c0001t0066g0011 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.121+2135C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657967 | ||||||
| chr22:17657979
|
G | A | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+2147G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657979 | ||||||
| chr22:17658005
|
A | G | 136 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(133): Show | 136 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.121+2173A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658005 | ||||||
| chr22:17658012
|
G | C | 5 | a0001c0001t0005g0143a0001c0001t0005g0145a0001c0001t0005g0149others(2): Show | 5 | HG01109.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+2180G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658012 | ||||||
| chr22:17658050
|
G | C | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+2218G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658050 | ||||||
| chr22:17658062
|
C | T | 2 | a0001c0009t0004g0157a0001c0009t0004g0158 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.121+2230C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658062 | ||||||
| chr22:17658096
|
G | C | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+2264G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658096 | ||||||
| chr22:17658119
|
C | T | 1 | a0001c0001t0003g0039 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.121+2287C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658119 | ||||||
| chr22:17658148
|
T | TTCTTCAT others(2830): Show |
1 | a0001c0001t0024g0243 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.121+2331_121+2332i others(2839): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17658148 | |||||
| chr22:17658148
|
T | TTCTTCAT others(2829): Show |
1 | a0001c0001t0024g0244 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.121+2331_121+2332i others(2838): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17658148 | |||||
| chr22:17658555
|
A | G | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.121+2723A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658555 | ||||||
| chr22:17658696
|
C | CA | 41 | a0001c0001t0003g0045a0001c0001t0003g0104a0001c0001t0006g0070others(38): Show | 41 | HG00099.hp2 HG00423.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.121+2882dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17658696 | |||||
| chr22:17658696
|
CA | C | 135 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.121+2882delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17658696 | |||||
| chr22:17658715
|
T | G | 252 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.121+2883T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658715 | ||||||
| chr22:17658785
|
A | G | 92 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.121+2953A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658785 | ||||||
| chr22:17658930
|
GCACCTGT others(2925): Show |
G | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+3119_121+6050d others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17658930 | |||||
| chr22:17659012
|
C | T | 1 | a0001c0001t0007g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.121+3180C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659012 | ||||||
| chr22:17659018
|
G | A | 4 | a0001c0002t0001g0261a0001c0002t0001g0287a0001c0002t0001g0288others(1): Show | 4 | HG02155.hp2 HG04184.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+3186G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659018 | ||||||
| chr22:17659049
|
C | T | 22 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.121+3217C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659049 | ||||||
| chr22:17659056
|
T | TA | 61 | a0001c0001t0002g0100a0001c0001t0002g0116a0001c0001t0002g0134others(58): Show | 61 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.121+3251dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17659056 | |||||
| chr22:17659056
|
T | TAA | 12 | a0001c0001t0005g0142a0001c0001t0007g0127a0001c0001t0008g0222others(9): Show | 12 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.121+3250_121+3251d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17659056 | |||||
| chr22:17659056
|
TA | T | 30 | a0001c0001t0003g0021a0001c0001t0003g0034a0001c0001t0003g0036others(27): Show | 30 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.121+3251delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17659056 | |||||
| chr22:17659056
|
TAA | T | 45 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0025others(42): Show | 45 | HG00140.hp2 HG00733.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.121+3250_121+3251d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17659056 | |||||
| chr22:17659181
|
T | C | 1 | a0001c0001t0007g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.121+3349T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659181 | ||||||
| chr22:17659221
|
A | G | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.121+3389A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659221 | ||||||
| chr22:17659288
|
T | C | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+3456T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659288 | ||||||
| chr22:17659345
|
C | G | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+3513C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659345 | ||||||
| chr22:17659457
|
C | T | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.121+3625C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659457 | ||||||
| chr22:17659488
|
C | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+3656C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659488 | ||||||
| chr22:17659656
|
G | A | 1 | a0001c0001t0005g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.121+3824G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659656 | ||||||
| chr22:17659660
|
AAAAAC | A | 51 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(48): Show | 51 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.121+3848_121+3852d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17659660 | |||||
| chr22:17659783
|
ACAG | A | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.121+3953_121+3955d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17659783 | |||||
| chr22:17660103
|
C | CA | 6 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(3): Show | 6 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+4272dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17660103 | |||||
| chr22:17660270
|
G | T | 2 | a0001c0002t0025g0074a0001c0002t0025g0075 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.121+4438G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660270 | ||||||
| chr22:17660357
|
G | A | 1 | a0001c0001t0003g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.121+4525G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660357 | ||||||
| chr22:17660358
|
A | T | 4 | a0001c0001t0006g0070a0001c0002t0006g0071a0001c0002t0006g0072others(1): Show | 4 | HG02145.hp1 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+4526A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660358 | ||||||
| chr22:17660493
|
C | T | 1 | a0001c0001t0005g0190 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.121+4661C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660493 | ||||||
| chr22:17660523
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.121+4691G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660523 | ||||||
| chr22:17660544
|
G | A | 13 | a0001c0001t0007g0008a0001c0001t0007g0009a0001c0001t0007g0012others(10): Show | 13 | HG01192.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+4712G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660544 | ||||||
| chr22:17660572
|
G | A | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121+4740G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660572 | ||||||
| chr22:17660615
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.121+4783A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660615 | ||||||
| chr22:17660651
|
C | T | 3 | a0001c0001t0002g0141a0001c0001t0033g0137a0001c0001t0053g0139 | 3 | HG00735.hp1 HG01081.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.121+4819C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660651 | ||||||
| chr22:17660718
|
C | A | 5 | a0001c0001t0005g0143a0001c0001t0005g0145a0001c0001t0005g0149others(2): Show | 5 | HG01109.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+4886C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660718 | ||||||
| chr22:17660814
|
G | C | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+4982G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660814 | ||||||
| chr22:17660933
|
T | C | 1 | a0001c0001t0003g0029 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.121+5101T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660933 | ||||||
| chr22:17660981
|
G | A | 1 | a0002c0003t0001g0268 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.121+5149G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660981 | ||||||
| chr22:17661069
|
C | T | 161 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.121+5237C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661069 | ||||||
| chr22:17661113
|
C | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+5281C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661113 | ||||||
| chr22:17661326
|
C | T | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121+5494C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661326 | ||||||
| chr22:17661398
|
T | C | 213 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(210): Show | 213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.121+5566T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661398 | ||||||
| chr22:17661504
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.121+5672G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661504 | ||||||
| chr22:17661549
|
A | C | 167 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(164): Show | 167 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.121+5717A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661549 | ||||||
| chr22:17661860
|
G | A | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+6028G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661860 | ||||||
| chr22:17661991
|
C | CA | 6 | a0001c0001t0002g0147a0001c0001t0005g0190a0004c0006t0001g0090others(3): Show | 6 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.121+6174dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17661991 | |||||
| chr22:17661991
|
CA | C | 7 | a0001c0001t0002g0209a0001c0001t0004g0136a0001c0001t0005g0241others(4): Show | 7 | HG00408.hp1 HG01261.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.121+6174delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17661991 | |||||
| chr22:17662058
|
T | A | 257 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.121+6226T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662058 | ||||||
| chr22:17662205
|
G | A | 2 | a0001c0001t0064g0304a0001c0001t0065g0103 | 2 | HG01255.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.121+6373G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662205 | ||||||
| chr22:17662245
|
A | G | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+6413A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662245 | ||||||
| chr22:17662304
|
T | C | 1 | a0001c0002t0042g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.121+6472T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662304 | ||||||
| chr22:17662305
|
C | A | 1 | a0001c0002t0042g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.121+6473C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662305 | ||||||
| chr22:17662324
|
A | G | 5 | a0001c0001t0009g0032a0001c0001t0009g0033a0001c0001t0009g0038others(2): Show | 5 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+6492A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662324 | ||||||
| chr22:17662696
|
A | G | 1 | a0001c0001t0011g0133 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.121+6864A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662696 | ||||||
| chr22:17662708
|
A | C | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+6876A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662708 | ||||||
| chr22:17662725
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+6893G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662725 | ||||||
| chr22:17663397
|
A | G | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+7565A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17663397 | ||||||
| chr22:17663440
|
G | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+7608G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17663440 | ||||||
| chr22:17663622
|
T | C | 252 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.121+7790T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17663622 | ||||||
| chr22:17663683
|
C | CT | 9 | a0001c0001t0008g0229a0001c0001t0036g0094a0001c0001t0039g0160others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.121+7869dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17663683 | |||||
| chr22:17663683
|
C | CTT | 159 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(156): Show | 159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.121+7868_121+7869d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17663683 | |||||
| chr22:17663683
|
C | CTTT | 11 | a0001c0001t0005g0145a0003c0004t0015g0080a0003c0004t0016g0087others(8): Show | 11 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.121+7867_121+7869d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17663683 | |||||
| chr22:17663757
|
G | A | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+7925G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17663757 | ||||||
| chr22:17663853
|
AT | A | 14 | a0001c0001t0041g0240a0003c0004t0015g0080a0003c0004t0015g0081others(11): Show | 14 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.121+8034delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17663853 | |||||
| chr22:17664205
|
G | A | 18 | a0001c0001t0003g0022a0001c0001t0003g0034a0001c0001t0003g0035others(15): Show | 18 | HG02135.hp2 NA18955.hp1 NA18965.hp2 others(15): Show |
intron_variant | MODIFIER | c.121+8373G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664205 | ||||||
| chr22:17664223
|
G | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+8391G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664223 | ||||||
| chr22:17664260
|
C | T | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.121+8428C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664260 | ||||||
| chr22:17664273
|
C | T | 1 | a0001c0001t0002g0209 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.121+8441C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664273 | ||||||
| chr22:17664291
|
C | T | 1 | a0001c0001t0005g0149 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+8459C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664291 | ||||||
| chr22:17664305
|
C | T | 161 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.121+8473C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664305 | ||||||
| chr22:17664383
|
T | C | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+8551T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664383 | ||||||
| chr22:17664415
|
AC | A | 19 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(16): Show | 19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.121+8592delC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17664415 | |||||
| chr22:17664415
|
ACC | A | 161 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.121+8591_121+8592d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17664415 | |||||
| chr22:17664445
|
A | G | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+8613A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664445 | ||||||
| chr22:17664542
|
A | C | 1 | a0001c0001t0011g0151 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.121+8710A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664542 | ||||||
| chr22:17664657
|
C | A | 159 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(156): Show | 159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.121+8825C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664657 | ||||||
| chr22:17664761
|
C | T | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+8929C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664761 | ||||||
| chr22:17664801
|
C | T | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+8969C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664801 | ||||||
| chr22:17664802
|
G | A | 23 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(20): Show | 23 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.121+8970G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664802 | ||||||
| chr22:17664861
|
C | G | 1 | a0001c0001t0029g0174 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.121+9029C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664861 | ||||||
| chr22:17665169
|
C | G | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+9337C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665169 | ||||||
| chr22:17665445
|
G | A | 1 | a0001c0001t0062g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.121+9613G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665445 | ||||||
| chr22:17665610
|
G | A | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+9778G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665610 | ||||||
| chr22:17665625
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+9793G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665625 | ||||||
| chr22:17665688
|
T | C | 252 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.121+9856T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665688 | ||||||
| chr22:17665688
|
T | G | 1 | a0002c0003t0001g0262 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.121+9856T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665688 | ||||||
| chr22:17665723
|
T | C | 21 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.121+9891T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665723 | ||||||
| chr22:17665830
|
A | G | 1 | a0001c0001t0004g0191 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.121+9998A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665830 | ||||||
| chr22:17665884
|
C | T | 1 | a0001c0001t0003g0002 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121+10052C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665884 | ||||||
| chr22:17666200
|
A | ATTTTTAT | 95 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(92): Show | 95 | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.121+10381_121+1038 others(11): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17666200 | |||||
| chr22:17666221
|
A | T | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+10389A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17666221 | ||||||
| chr22:17666271
|
A | C | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+10439A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17666271 | ||||||
| chr22:17666678
|
C | CT | 162 | a0001c0001t0002g0100a0001c0001t0002g0112a0001c0001t0002g0116others(159): Show | 162 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.121+10867dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17666678 | |||||
| chr22:17666678
|
CT | C | 10 | a0001c0001t0003g0026a0001c0001t0003g0037a0001c0001t0003g0041others(7): Show | 10 | HG00280.hp2 HG01169.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.121+10867delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17666678 | |||||
| chr22:17666998
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+11166G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17666998 | ||||||
| chr22:17667166
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+11334G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667166 | ||||||
| chr22:17667167
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+11335G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667167 | ||||||
| chr22:17667185
|
T | C | 1 | a0001c0001t0061g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.121+11353T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667185 | ||||||
| chr22:17667204
|
C | T | 1 | a0001c0001t0002g0189 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.121+11372C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667204 | ||||||
| chr22:17667205
|
C | G | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121+11373C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667205 | ||||||
| chr22:17667376
|
G | A | 1 | a0001c0001t0055g0129 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.121+11544G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667376 | ||||||
| chr22:17667417
|
C | T | 1 | a0001c0001t0034g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.121+11585C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667417 | ||||||
| chr22:17667418
|
G | A | 2 | a0001c0002t0026g0299a0001c0002t0026g0300 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.121+11586G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667418 | ||||||
| chr22:17667609
|
A | G | 1 | a0001c0001t0005g0142 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.121+11777A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667609 | ||||||
| chr22:17667721
|
C | G | 7 | a0001c0001t0002g0116a0001c0001t0002g0138a0001c0001t0002g0141others(4): Show | 7 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.121+11889C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667721 | ||||||
| chr22:17667754
|
C | G | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121+11922C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667754 | ||||||
| chr22:17667754
|
C | T | 1 | a0001c0001t0003g0002 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121+11922C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667754 | ||||||
| chr22:17667854
|
CATGATTG others(8): Show |
C | 1 | a0001c0001t0003g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.121+12023_121+1203 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667854 | ||||||
| chr22:17667899
|
C | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+12067C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667899 | ||||||
| chr22:17667963
|
CT | C | 202 | a0001c0001t0002g0100a0001c0001t0002g0111a0001c0001t0002g0112others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.121+12152delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17667963 | |||||
| chr22:17667963
|
CTT | C | 27 | a0001c0001t0002g0099a0001c0001t0003g0054a0001c0001t0004g0191others(24): Show | 27 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.121+12151_121+1215 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17667963 | |||||
| chr22:17668018
|
C | CT | 44 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(41): Show | 44 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.121+12198dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17668018 | |||||
| chr22:17668042
|
G | A | 1 | a0002c0003t0058g0275 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.121+12210G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668042 | ||||||
| chr22:17668075
|
A | G | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+12243A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668075 | ||||||
| chr22:17668156
|
G | T | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.121+12324G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668156 | ||||||
| chr22:17668302
|
C | T | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+12470C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668302 | ||||||
| chr22:17668487
|
C | G | 4 | a0001c0001t0004g0098a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02738.hp1 HG03834.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+12655C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668487 | ||||||
| chr22:17668714
|
C | G | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+12882C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668714 | ||||||
| chr22:17668745
|
G | A | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+12913G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668745 | ||||||
| chr22:17668816
|
A | C | 1 | a0001c0001t0002g0213 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.121+12984A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668816 | ||||||
| chr22:17668850
|
C | G | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+13018C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668850 | ||||||
| chr22:17668978
|
C | T | 1 | a0001c0002t0069g0294 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.121+13146C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668978 | ||||||
| chr22:17669030
|
C | CT | 18 | a0001c0001t0002g0216a0001c0001t0003g0251a0001c0001t0004g0191others(15): Show | 18 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.121+13218dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17669030 | |||||
| chr22:17669030
|
C | CTT | 138 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.121+13217_121+1321 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17669030 | |||||
| chr22:17669030
|
C | CTTT | 22 | a0001c0001t0002g0210a0001c0001t0007g0008a0001c0001t0008g0222others(19): Show | 22 | HG01169.hp2 HG01175.hp1 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.121+13216_121+1321 others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17669030 | |||||
| chr22:17669030
|
CT | C | 23 | a0001c0001t0003g0021a0001c0001t0003g0041a0001c0001t0006g0070others(20): Show | 23 | HG00099.hp2 HG00738.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.121+13218delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17669030 | |||||
| chr22:17669030
|
CTT | C | 6 | a0001c0002t0014g0061a0001c0002t0014g0063a0001c0002t0014g0064others(3): Show | 6 | HG01261.hp2 HG02717.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+13217_121+1321 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17669030 | |||||
| chr22:17669034
|
T | C | 1 | a0001c0002t0001g0257 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.121+13202T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669034 | ||||||
| chr22:17669056
|
G | A | 3 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0204 | 3 | HG03927.hp1 HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.121+13224G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669056 | ||||||
| chr22:17669146
|
C | T | 1 | a0001c0001t0004g0191 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.121+13314C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669146 | ||||||
| chr22:17669190
|
AC | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+13361delC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17669190 | |||||
| chr22:17669278
|
C | T | 5 | a0001c0001t0066g0011a0004c0006t0001g0090a0004c0006t0001g0092others(2): Show | 5 | HG02109.hp2 HG02280.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+13446C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669278 | ||||||
| chr22:17669412
|
A | G | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.121+13580A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669412 | ||||||
| chr22:17669414
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+13582G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669414 | ||||||
| chr22:17669662
|
G | T | 1 | a0006c0010t0001g0263 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.122-13552G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669662 | ||||||
| chr22:17669712
|
G | A | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.122-13502G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669712 | ||||||
| chr22:17669942
|
A | G | 1 | a0001c0001t0046g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.122-13272A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669942 | ||||||
| chr22:17669950
|
A | C | 1 | a0001c0001t0062g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.122-13264A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669950 | ||||||
| chr22:17670076
|
T | C | 2 | a0001c0001t0013g0164a0001c0001t0013g0184 | 2 | NA18943.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.122-13138T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17670076 | ||||||
| chr22:17670243
|
T | G | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-12971T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17670243 | ||||||
| chr22:17670373
|
C | CT | 50 | a0001c0001t0002g0111a0001c0001t0002g0154a0001c0001t0003g0045others(47): Show | 50 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.122-12823dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17670373 | |||||
| chr22:17670373
|
C | CTT | 133 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0112others(130): Show | 133 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.122-12824_122-1282 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17670373 | |||||
| chr22:17670373
|
C | CTTT | 6 | a0001c0001t0002g0210a0001c0001t0002g0245a0001c0001t0004g0155others(3): Show | 6 | HG01175.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-12825_122-1282 others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17670373 | |||||
| chr22:17670517
|
G | A | 3 | a0001c0001t0020g0224a0001c0001t0020g0231a0001c0001t0020g0233 | 3 | HG02257.hp1 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.122-12697G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17670517 | ||||||
| chr22:17670566
|
G | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-12648G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17670566 | ||||||
| chr22:17670834
|
A | G | 1 | a0001c0001t0003g0024 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.122-12380A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17670834 | ||||||
| chr22:17671000
|
C | T | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.122-12214C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671000 | ||||||
| chr22:17671142
|
G | A | 1 | a0001c0001t0005g0242 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.122-12072G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671142 | ||||||
| chr22:17671146
|
A | G | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-12068A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671146 | ||||||
| chr22:17671155
|
G | C | 1 | a0001c0001t0004g0136 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.122-12059G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671155 | ||||||
| chr22:17671287
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-11927G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671287 | ||||||
| chr22:17671318
|
C | T | 5 | a0001c0001t0046g0023a0004c0006t0001g0090a0004c0006t0001g0092others(2): Show | 5 | HG01243.hp1 HG02280.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-11896C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671318 | ||||||
| chr22:17671350
|
C | T | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.122-11864C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671350 | ||||||
| chr22:17671369
|
G | C | 3 | a0001c0001t0002g0134a0001c0001t0002g0162a0001c0001t0056g0214 | 3 | HG02132.hp1 NA18952.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.122-11845G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671369 | ||||||
| chr22:17671381
|
G | C | 180 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(177): Show | 180 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.122-11833G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671381 | ||||||
| chr22:17671393
|
CA | C | 35 | a0001c0001t0002g0138a0001c0001t0002g0198a0001c0001t0002g0199others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.122-11797delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17671393 | |||||
| chr22:17671393
|
CAA | C | 209 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.122-11798_122-1179 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17671393 | |||||
| chr22:17671393
|
CAAA | C | 8 | a0001c0001t0003g0050a0001c0001t0024g0243a0001c0001t0046g0023others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.122-11799_122-1179 others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17671393 | |||||
| chr22:17671436
|
G | A | 2 | a0001c0001t0005g0117a0001c0001t0005g0179 | 2 | NA18956.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.122-11778G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671436 | ||||||
| chr22:17671519
|
A | T | 180 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(177): Show | 180 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.122-11695A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671519 | ||||||
| chr22:17671565
|
CA | C | 242 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.122-11634delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17671565 | |||||
| chr22:17671612
|
A | G | 1 | a0001c0001t0033g0137 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.122-11602A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671612 | ||||||
| chr22:17671630
|
A | G | 1 | a0001c0001t0002g0203 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.122-11584A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671630 | ||||||
| chr22:17671632
|
G | T | 18 | a0001c0002t0001g0124a0001c0002t0001g0257a0001c0002t0001g0258others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.122-11582G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671632 | ||||||
| chr22:17671712
|
A | G | 1 | a0001c0007t0009g0053 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.122-11502A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671712 | ||||||
| chr22:17672008
|
C | G | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.122-11206C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17672008 | ||||||
| chr22:17672112
|
A | G | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-11102A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17672112 | ||||||
| chr22:17672202
|
A | C | 1 | a0001c0001t0007g0248 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.122-11012A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17672202 | ||||||
| chr22:17672645
|
G | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.122-10569G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17672645 | ||||||
| chr22:17672778
|
T | A | 1 | a0001c0001t0003g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.122-10436T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17672778 | ||||||
| chr22:17673255
|
C | G | 13 | a0001c0001t0003g0002a0001c0001t0003g0024a0001c0001t0003g0025others(10): Show | 13 | HG02572.hp2 HG02630.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.122-9959C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673255 | ||||||
| chr22:17673300
|
A | G | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.122-9914A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673300 | ||||||
| chr22:17673333
|
C | A | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.122-9881C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673333 | ||||||
| chr22:17673334
|
A | G | 13 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(10): Show | 13 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.122-9880A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673334 | ||||||
| chr22:17673361
|
CT | C | 121 | a0001c0001t0002g0168a0001c0001t0003g0002a0001c0001t0003g0021others(118): Show | 121 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.122-9835delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17673361 | |||||
| chr22:17673361
|
CTT | C | 109 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.122-9836_122-9835d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17673361 | |||||
| chr22:17673395
|
T | C | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-9819T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673395 | ||||||
| chr22:17673398
|
G | A | 1 | a0001c0001t0003g0104 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.122-9816G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673398 | ||||||
| chr22:17673513
|
G | A | 1 | a0001c0001t0011g0151 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.122-9701G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673513 | ||||||
| chr22:17673533
|
A | AT | 7 | a0001c0002t0001g0095a0001c0002t0001g0265a0001c0002t0012g0003others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-9664dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17673533 | |||||
| chr22:17673533
|
AT | A | 207 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(204): Show | 207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.122-9664delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17673533 | |||||
| chr22:17673533
|
ATT | A | 12 | a0001c0001t0002g0128a0001c0001t0003g0024a0001c0001t0003g0025others(9): Show | 12 | HG01070.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.122-9665_122-9664d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17673533 | |||||
| chr22:17673619
|
C | T | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.122-9595C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673619 | ||||||
| chr22:17673629
|
G | A | 161 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.122-9585G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673629 | ||||||
| chr22:17673861
|
G | A | 1 | a0001c0001t0004g0131 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.122-9353G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673861 | ||||||
| chr22:17673870
|
A | G | 1 | a0001c0002t0001g0264 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.122-9344A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673870 | ||||||
| chr22:17673878
|
A | G | 161 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.122-9336A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673878 | ||||||
| chr22:17674021
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-9193G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674021 | ||||||
| chr22:17674135
|
G | A | 4 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0118others(1): Show | 4 | HG02896.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-9079G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674135 | ||||||
| chr22:17674460
|
G | A | 1 | a0001c0001t0010g0238 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.122-8754G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674460 | ||||||
| chr22:17674516
|
A | G | 210 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(207): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.122-8698A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674516 | ||||||
| chr22:17674537
|
C | T | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-8677C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674537 | ||||||
| chr22:17674605
|
CAA | C | 237 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.122-8593_122-8592d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17674605 | |||||
| chr22:17674605
|
CAAA | C | 13 | a0001c0001t0003g0251a0001c0001t0007g0108a0001c0001t0007g0109others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-8594_122-8592d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17674605 | |||||
| chr22:17674701
|
A | G | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.122-8513A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674701 | ||||||
| chr22:17674886
|
T | TATA | 253 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.122-8326_122-8325i others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17674886 | |||||
| chr22:17674926
|
A | T | 2 | a0001c0002t0026g0299a0001c0002t0026g0300 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.122-8288A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674926 | ||||||
| chr22:17675075
|
TAC | T | 181 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(178): Show | 181 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.122-8123_122-8122d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17675075 | |||||
| chr22:17675279
|
G | A | 1 | a0001c0002t0001g0261 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.122-7935G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675279 | ||||||
| chr22:17675346
|
C | T | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.122-7868C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675346 | ||||||
| chr22:17675372
|
T | C | 1 | a0001c0002t0027g0006 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.122-7842T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675372 | ||||||
| chr22:17675403
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-7811G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675403 | ||||||
| chr22:17675435
|
G | A | 3 | a0001c0001t0004g0098a0001c0001t0004g0200a0001c0001t0004g0201 | 3 | HG02738.hp1 HG03834.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.122-7779G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675435 | ||||||
| chr22:17675578
|
C | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-7636C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675578 | ||||||
| chr22:17675605
|
G | A | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-7609G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675605 | ||||||
| chr22:17675660
|
C | T | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.122-7554C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675660 | ||||||
| chr22:17675677
|
T | C | 1 | a0001c0001t0050g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.122-7537T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675677 | ||||||
| chr22:17675889
|
A | C | 1 | a0001c0001t0010g0219 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.122-7325A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675889 | ||||||
| chr22:17676119
|
T | C | 1 | a0001c0001t0010g0238 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.122-7095T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676119 | ||||||
| chr22:17676276
|
A | C | 1 | a0001c0001t0003g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.122-6938A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676276 | ||||||
| chr22:17676305
|
CA | C | 253 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.122-6900delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17676305 | |||||
| chr22:17676336
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-6878G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676336 | ||||||
| chr22:17676545
|
A | G | 1 | a0001c0001t0067g0170 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.122-6669A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676545 | ||||||
| chr22:17676641
|
T | C | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.122-6573T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676641 | ||||||
| chr22:17676902
|
A | G | 2 | a0001c0001t0002g0176a0001c0001t0002g0195 | 2 | HG01069.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.122-6312A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676902 | ||||||
| chr22:17676902
|
A | T | 1 | a0001c0001t0003g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.122-6312A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676902 | ||||||
| chr22:17676938
|
A | G | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.122-6276A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676938 | ||||||
| chr22:17677154
|
CAAAAAAT others(1): Show |
C | 4 | a0001c0001t0002g0116a0001c0001t0002g0138a0001c0001t0002g0188others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-6040_122-6033d others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17677154 | |||||
| chr22:17677156
|
A | G | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-6058A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677156 | ||||||
| chr22:17677163
|
A | G | 1 | a0001c0001t0020g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.122-6051A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677163 | ||||||
| chr22:17677180
|
A | G | 159 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(156): Show | 159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.122-6034A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677180 | ||||||
| chr22:17677247
|
T | C | 2 | a0002c0003t0001g0279a0002c0003t0001g0280 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.122-5967T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677247 | ||||||
| chr22:17677258
|
T | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-5956T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677258 | ||||||
| chr22:17677533
|
A | G | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-5681A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677533 | ||||||
| chr22:17677688
|
A | C | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-5526A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677688 | ||||||
| chr22:17677837
|
A | G | 1 | a0001c0001t0021g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.122-5377A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677837 | ||||||
| chr22:17677838
|
T | C | 1 | a0001c0001t0046g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.122-5376T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677838 | ||||||
| chr22:17677867
|
C | CA | 20 | a0001c0001t0005g0161a0001c0001t0007g0096a0001c0001t0011g0151others(17): Show | 20 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.122-5337dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17677867 | |||||
| chr22:17677878
|
C | A | 5 | a0001c0002t0012g0003a0004c0006t0001g0090a0004c0006t0001g0092others(2): Show | 5 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-5336C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677878 | ||||||
| chr22:17677886
|
C | A | 4 | a0001c0001t0002g0099a0001c0001t0002g0126a0001c0001t0002g0175others(1): Show | 4 | NA18984.hp1 NA19056.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-5328C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677886 | ||||||
| chr22:17677989
|
T | C | 1 | a0001c0001t0007g0127 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.122-5225T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677989 | ||||||
| chr22:17678115
|
C | T | 136 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(133): Show | 136 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.122-5099C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678115 | ||||||
| chr22:17678148
|
G | A | 1 | a0002c0003t0001g0278 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.122-5066G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678148 | ||||||
| chr22:17678263
|
A | G | 2 | a0001c0001t0005g0185a0001c0001t0005g0241 | 2 | HG00408.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.122-4951A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678263 | ||||||
| chr22:17678302
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.122-4912G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678302 | ||||||
| chr22:17678377
|
C | T | 1 | a0001c0001t0039g0160 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.122-4837C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678377 | ||||||
| chr22:17678410
|
A | G | 1 | a0001c0001t0007g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122-4804A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678410 | ||||||
| chr22:17678693
|
T | G | 1 | a0001c0001t0002g0176 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.122-4521T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678693 | ||||||
| chr22:17678703
|
C | T | 1 | a0001c0001t0011g0151 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.122-4511C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678703 | ||||||
| chr22:17678777
|
G | A | 20 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(17): Show | 20 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.122-4437G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678777 | ||||||
| chr22:17678878
|
A | T | 1 | a0001c0002t0001g0290 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.122-4336A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678878 | ||||||
| chr22:17678996
|
A | G | 1 | a0001c0001t0002g0186 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.122-4218A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678996 | ||||||
| chr22:17679213
|
G | A | 72 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.122-4001G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679213 | ||||||
| chr22:17679226
|
G | A | 1 | a0001c0001t0005g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.122-3988G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679226 | ||||||
| chr22:17679248
|
GTCAATTG others(2905): Show |
G | 1 | a0001c0002t0037g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.122-3963_122-1052d others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17679248 | |||||
| chr22:17679264
|
C | CT | 9 | a0001c0001t0003g0027a0001c0001t0003g0050a0001c0001t0009g0038others(6): Show | 9 | HG01256.hp2 HG01517.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.122-3926dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17679264 | |||||
| chr22:17679264
|
C | CTT | 19 | a0001c0001t0006g0070a0001c0001t0066g0011a0001c0002t0006g0066others(16): Show | 19 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.122-3927_122-3926d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17679264 | |||||
| chr22:17679264
|
CT | C | 12 | a0001c0001t0002g0128a0001c0001t0002g0204a0001c0001t0002g0210others(9): Show | 12 | HG01070.hp2 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122-3926delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17679264 | |||||
| chr22:17679264
|
CTT | C | 161 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.122-3927_122-3926d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17679264 | |||||
| chr22:17679264
|
CTTT | C | 7 | a0001c0001t0005g0161a0001c0001t0011g0113a0001c0001t0067g0170others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-3928_122-3926d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17679264 | |||||
| chr22:17679290
|
A | G | 2 | a0001c0001t0003g0251a0001c0001t0003g0252 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.122-3924A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679290 | ||||||
| chr22:17679296
|
T | C | 1 | a0001c0002t0035g0301 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.122-3918T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679296 | ||||||
| chr22:17679312
|
C | T | 7 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-3902C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679312 | ||||||
| chr22:17679414
|
C | T | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-3800C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679414 | ||||||
| chr22:17679539
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-3675G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679539 | ||||||
| chr22:17679932
|
G | A | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-3282G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679932 | ||||||
| chr22:17679960
|
C | G | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-3254C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679960 | ||||||
| chr22:17680016
|
C | A | 4 | a0001c0002t0006g0068a0001c0002t0006g0069a0001c0002t0006g0073others(1): Show | 4 | HG02071.hp1 HG02602.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-3198C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680016 | ||||||
| chr22:17680071
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-3143G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680071 | ||||||
| chr22:17680137
|
C | T | 1 | a0001c0001t0005g0190 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.122-3077C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680137 | ||||||
| chr22:17680188
|
C | T | 6 | a0001c0001t0017g0013a0001c0001t0017g0019a0001c0001t0017g0020others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-3026C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680188 | ||||||
| chr22:17680200
|
G | A | 1 | a0001c0001t0003g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.122-3014G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680200 | ||||||
| chr22:17680215
|
C | CAA | 45 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(42): Show | 45 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.122-2986_122-2985d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | |||||
| chr22:17680215
|
C | CAAAAAAA others(1): Show |
9 | a0001c0001t0002g0100a0001c0001t0002g0212a0001c0001t0007g0248others(6): Show | 9 | HG02717.hp2 HG03041.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.122-2992_122-2985d others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | |||||
| chr22:17680215
|
C | CAAAAAAA others(2): Show |
141 | a0001c0001t0002g0099a0001c0001t0002g0111a0001c0001t0002g0112others(138): Show | 141 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.122-2993_122-2985d others(11): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | |||||
| chr22:17680215
|
C | CAAAAAAA others(3): Show |
10 | a0001c0001t0002g0189a0001c0001t0002g0203a0001c0001t0005g0060others(7): Show | 10 | HG01255.hp2 HG02148.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.122-2994_122-2985d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | |||||
| chr22:17680215
|
C | CAAAAAAA others(4): Show |
13 | a0003c0004t0015g0081a0003c0004t0015g0253a0003c0004t0016g0087others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-2995_122-2985d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | |||||
| chr22:17680215
|
C | CAAAAAAA others(5): Show |
7 | a0001c0001t0005g0161a0003c0004t0015g0080a0003c0004t0016g0089others(4): Show | 7 | HG01361.hp1 HG02055.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-2996_122-2985d others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | |||||
| chr22:17680215
|
C | CAAAAAAA others(6): Show |
1 | a0005c0008t0019g0256 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.122-2997_122-2985d others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | |||||
| chr22:17680240
|
G | A | 3 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091 | 3 | HG02886.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.122-2974G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680240 | ||||||
| chr22:17680311
|
C | T | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.122-2903C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680311 | ||||||
| chr22:17680370
|
A | C | 252 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.122-2844A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680370 | ||||||
| chr22:17680379
|
G | A | 6 | a0001c0001t0017g0013a0001c0001t0017g0019a0001c0001t0017g0020others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-2835G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680379 | ||||||
| chr22:17680392
|
C | T | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.122-2822C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680392 | ||||||
| chr22:17680511
|
C | CA | 38 | a0001c0001t0002g0195a0001c0001t0003g0022a0001c0001t0003g0025others(35): Show | 38 | HG00140.hp2 HG00544.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.122-2673dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680511 | |||||
| chr22:17680511
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0028g0303 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.122-2699_122-2673d others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680511 | |||||
| chr22:17680518
|
AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0046g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.122-2688_122-2665d others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680518 | |||||
| chr22:17680521
|
AAAAAAAA others(14): Show |
A | 9 | a0001c0001t0002g0099a0001c0001t0002g0175a0001c0001t0007g0108others(6): Show | 9 | HG01255.hp2 HG02717.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.122-2685_122-2665d others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680521 | |||||
| chr22:17680522
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0064g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.122-2684_122-2665d others(22): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680522 | |||||
| chr22:17680523
|
AAAAAAAA others(12): Show |
A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-2683_122-2665d others(21): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680523 | |||||
| chr22:17680524
|
AAAAAAAA others(11): Show |
A | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.122-2682_122-2665d others(20): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680524 | |||||
| chr22:17680525
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0002g0154 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.122-2681_122-2665d others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680525 | |||||
| chr22:17680527
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0005g0182 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.122-2679_122-2665d others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680527 | |||||
| chr22:17680528
|
AAAAAAAA others(7): Show |
A | 21 | a0001c0001t0006g0070a0001c0001t0008g0230a0001c0001t0021g0018others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.122-2678_122-2665d others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680528 | |||||
| chr22:17680529
|
AAAAAAAA others(6): Show |
A | 5 | a0001c0002t0014g0061a0001c0002t0014g0063a0001c0002t0014g0064others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-2677_122-2665d others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680529 | |||||
| chr22:17680531
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0003g0029 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.122-2675_122-2665d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680531 | |||||
| chr22:17680532
|
AAAAAAAA others(3): Show |
A | 4 | a0001c0001t0003g0024a0001c0001t0003g0057a0001c0001t0003g0058others(1): Show | 4 | HG02630.hp2 HG02922.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-2674_122-2665d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680532 | |||||
| chr22:17680538
|
AAAAG | A | 44 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0128others(41): Show | 44 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.122-2672_122-2669d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680538 | |||||
| chr22:17680539
|
AAAG | A | 43 | a0001c0001t0002g0100a0001c0001t0002g0116a0001c0001t0002g0126others(40): Show | 43 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.122-2672_122-2670d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680539 | |||||
| chr22:17680540
|
AAG | A | 31 | a0001c0001t0002g0141a0001c0001t0002g0144a0001c0001t0002g0150others(28): Show | 31 | HG00609.hp1 HG00609.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.122-2672_122-2671d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680540 | |||||
| chr22:17680541
|
AG | A | 19 | a0001c0001t0002g0199a0001c0001t0002g0204a0001c0001t0003g0251others(16): Show | 19 | HG00423.hp2 HG01168.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.122-2672delG | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680541 | ||||||
| chr22:17680542
|
G | A | 48 | a0001c0001t0002g0189a0001c0001t0002g0195a0001c0001t0003g0002others(45): Show | 48 | HG00140.hp2 HG00733.hp1 HG01496.hp2 others(45): Show |
intron_variant | MODIFIER | c.122-2672G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680542 | ||||||
| chr22:17680773
|
G | A | 158 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(155): Show | 158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.122-2441G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680773 | ||||||
| chr22:17680990
|
G | A | 2 | a0001c0001t0013g0164a0001c0001t0013g0165 | 2 | NA19007.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.122-2224G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680990 | ||||||
| chr22:17681029
|
C | T | 20 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(17): Show | 20 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.122-2185C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681029 | ||||||
| chr22:17681142
|
A | C | 1 | a0001c0002t0035g0301 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.122-2072A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681142 | ||||||
| chr22:17681159
|
G | A | 1 | a0001c0001t0007g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122-2055G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681159 | ||||||
| chr22:17681161
|
A | T | 3 | a0001c0007t0009g0053a0001c0007t0009g0056a0001c0007t0044g0052 | 3 | HG03130.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.122-2053A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681161 | ||||||
| chr22:17681315
|
G | C | 1 | a0001c0001t0005g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.122-1899G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681315 | ||||||
| chr22:17681386
|
G | C | 1 | a0002c0003t0001g0272 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.122-1828G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681386 | ||||||
| chr22:17681498
|
G | GA | 50 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(47): Show | 50 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.122-1703dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17681498 | |||||
| chr22:17681535
|
A | C | 1 | a0001c0001t0005g0161 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.122-1679A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681535 | ||||||
| chr22:17681622
|
A | G | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-1592A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681622 | ||||||
| chr22:17681763
|
C | T | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-1451C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681763 | ||||||
| chr22:17681812
|
T | A | 3 | a0001c0001t0020g0224a0001c0001t0020g0231a0001c0001t0020g0233 | 3 | HG02257.hp1 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.122-1402T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681812 | ||||||
| chr22:17681836
|
G | A | 15 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(12): Show | 15 | HG00099.hp2 HG00738.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.122-1378G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681836 | ||||||
| chr22:17681899
|
G | A | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-1315G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681899 | ||||||
| chr22:17681909
|
A | G | 5 | a0001c0001t0005g0143a0001c0001t0005g0145a0001c0001t0005g0149others(2): Show | 5 | HG01109.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-1305A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681909 | ||||||
| chr22:17681928
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-1286G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681928 | ||||||
| chr22:17681976
|
G | C | 4 | a0001c0002t0014g0061a0001c0002t0014g0063a0001c0002t0014g0064others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-1238G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681976 | ||||||
| chr22:17682007
|
T | C | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-1207T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682007 | ||||||
| chr22:17682098
|
A | G | 136 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(133): Show | 136 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.122-1116A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682098 | ||||||
| chr22:17682100
|
T | C | 20 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(17): Show | 20 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.122-1114T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682100 | ||||||
| chr22:17682310
|
T | C | 4 | a0001c0001t0008g0223a0001c0001t0010g0146a0001c0001t0010g0235others(1): Show | 4 | NA18946.hp2 NA18953.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-904T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682310 | ||||||
| chr22:17682604
|
T | C | 2 | a0001c0001t0002g0199a0001c0001t0002g0204 | 2 | HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.122-610T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682604 | ||||||
| chr22:17682872
|
G | A | 45 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(42): Show | 45 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.122-342G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682872 | ||||||
| chr22:17682964
|
C | T | 1 | a0001c0001t0005g0148 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.122-250C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682964 | ||||||
| chr22:17683119
|
C | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0241 | 2 | HG00408.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.122-95C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17683119 | ||||||
| chr22:17683132
|
C | CAA | 15 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.122-67_122-66dupAA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17683132 | |||||
| chr22:17683132
|
CA | C | 26 | a0001c0001t0002g0126a0001c0001t0003g0048a0001c0001t0006g0070others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.122-66delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17683132 | |||||
| chr22:17683360
|
G | T | 1 | a0001c0001t0003g0024 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.229+39G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683360 | ||||||
| chr22:17683539
|
A | G | 1 | a0001c0001t0018g0171 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.229+218A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683539 | ||||||
| chr22:17683728
|
C | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+407C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683728 | ||||||
| chr22:17683729
|
A | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+408A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683729 | ||||||
| chr22:17683731
|
C | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+410C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683731 | ||||||
| chr22:17683734
|
TATA | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+414_229+416del others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683734 | ||||||
| chr22:17683735
|
A | T | 9 | a0001c0001t0002g0099a0001c0001t0002g0126a0001c0001t0002g0156others(6): Show | 9 | HG01192.hp2 HG01978.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.229+414A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683735 | ||||||
| chr22:17683801
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+480G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683801 | ||||||
| chr22:17683844
|
C | CATT | 64 | a0001c0001t0002g0195a0001c0001t0003g0021a0001c0001t0003g0022others(61): Show | 64 | HG00140.hp2 HG00733.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.229+561_229+563dup others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17683844 | |||||
| chr22:17683844
|
C | CATTATT | 3 | a0001c0001t0003g0029a0001c0002t0001g0257a0001c0002t0012g0003 | 3 | HG02970.hp2 HG03486.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.229+558_229+563dup others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17683844 | |||||
| chr22:17683844
|
CATT | C | 14 | a0001c0001t0013g0236a0001c0001t0066g0011a0001c0002t0001g0124others(11): Show | 14 | HG00423.hp1 HG01109.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.229+561_229+563del others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17683844 | |||||
| chr22:17683844
|
CATTATT | C | 16 | a0001c0001t0002g0099a0001c0001t0002g0126a0001c0001t0002g0156others(13): Show | 16 | HG00438.hp2 HG00544.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.229+558_229+563del others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17683844 | |||||
| chr22:17683844
|
CATTATTA others(2): Show |
C | 145 | a0001c0001t0002g0100a0001c0001t0002g0111a0001c0001t0002g0112others(142): Show | 145 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.229+555_229+563del others(9): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17683844 | |||||
| chr22:17683914
|
G | T | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.229+593G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683914 | ||||||
| chr22:17683975
|
T | C | 21 | a0001c0002t0035g0301a0003c0004t0015g0080a0003c0004t0015g0081others(18): Show | 21 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.229+654T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683975 | ||||||
| chr22:17683981
|
C | G | 1 | a0001c0001t0005g0148 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.229+660C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683981 | ||||||
| chr22:17684040
|
C | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+719C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684040 | ||||||
| chr22:17684071
|
C | T | 4 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0118others(1): Show | 4 | HG02896.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+750C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684071 | ||||||
| chr22:17684078
|
A | G | 1 | a0001c0001t0006g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.229+757A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684078 | ||||||
| chr22:17684187
|
T | G | 1 | a0001c0001t0002g0169 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.229+866T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684187 | ||||||
| chr22:17684194
|
A | G | 2 | a0001c0001t0002g0212a0001c0001t0057g0125 | 2 | HG02602.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.229+873A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684194 | ||||||
| chr22:17684569
|
T | G | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+1248T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684569 | ||||||
| chr22:17684591
|
T | G | 1 | a0002c0003t0001g0272 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.229+1270T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684591 | ||||||
| chr22:17684712
|
T | C | 194 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.229+1391T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684712 | ||||||
| chr22:17684726
|
GCTAATTT others(162): Show |
G | 1 | a0003c0004t0016g0089 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.229+1424_229+1592d others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17684726 | |||||
| chr22:17684739
|
A | AT | 18 | a0001c0001t0002g0116a0001c0001t0003g0042a0001c0001t0005g0185others(15): Show | 18 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.229+1432dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17684739 | |||||
| chr22:17684765
|
G | A | 1 | a0003c0005t0006g0084 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.229+1444G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684765 | ||||||
| chr22:17684848
|
T | G | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.229+1527T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684848 | ||||||
| chr22:17684860
|
G | A | 138 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.229+1539G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684860 | ||||||
| chr22:17684881
|
T | C | 4 | a0001c0001t0003g0024a0001c0001t0008g0227a0002c0003t0001g0271others(1): Show | 4 | HG00280.hp2 HG00423.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+1560T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684881 | ||||||
| chr22:17684882
|
G | A | 1 | a0001c0001t0003g0024 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.229+1561G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684882 | ||||||
| chr22:17684923
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.229+1602G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684923 | ||||||
| chr22:17684934
|
G | A | 1 | a0001c0001t0004g0130 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.229+1613G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684934 | ||||||
| chr22:17684939
|
A | G | 1 | a0001c0001t0004g0163 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.229+1618A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684939 | ||||||
| chr22:17684940
|
G | A | 1 | a0001c0001t0004g0208 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.229+1619G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684940 | ||||||
| chr22:17685015
|
A | G | 25 | a0001c0001t0002g0172a0001c0001t0002g0245a0001c0001t0004g0155others(22): Show | 25 | HG01123.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.229+1694A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685015 | ||||||
| chr22:17685093
|
T | C | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.229+1772T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685093 | ||||||
| chr22:17685110
|
G | C | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.229+1789G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685110 | ||||||
| chr22:17685301
|
C | G | 2 | a0001c0001t0002g0203a0001c0001t0002g0213 | 2 | NA18964.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.229+1980C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685301 | ||||||
| chr22:17685366
|
C | T | 3 | a0001c0001t0008g0226a0001c0001t0008g0229a0001c0001t0038g0228 | 3 | HG03041.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.229+2045C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685366 | ||||||
| chr22:17685416
|
G | T | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0118 | 3 | HG03195.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.229+2095G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685416 | ||||||
| chr22:17685445
|
A | G | 1 | a0001c0001t0002g0186 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.229+2124A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685445 | ||||||
| chr22:17685512
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.229+2191C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685512 | ||||||
| chr22:17685557
|
T | C | 3 | a0001c0002t0026g0299a0001c0002t0026g0300a0001c0002t0035g0301 | 3 | HG02258.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.229+2236T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685557 | ||||||
| chr22:17685671
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.229+2350A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685671 | ||||||
| chr22:17685692
|
A | T | 1 | a0001c0001t0055g0129 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.229+2371A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685692 | ||||||
| chr22:17685736
|
A | G | 1 | a0001c0001t0010g0238 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.229+2415A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685736 | ||||||
| chr22:17685754
|
CTTTTTCT others(3): Show |
C | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.229+2439_229+2448d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685754 | |||||
| chr22:17685754
|
CTTTTTCT others(6): Show |
C | 1 | a0001c0001t0005g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.229+2439_229+2451d others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685754 | |||||
| chr22:17685760
|
C | CT | 21 | a0001c0001t0003g0027a0001c0001t0003g0030a0001c0001t0003g0042others(18): Show | 21 | HG00140.hp1 HG00735.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.229+2468dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
C | CTTTTT | 15 | a0001c0001t0002g0196a0001c0001t0002g0210a0001c0001t0002g0212others(12): Show | 15 | HG01074.hp1 HG01175.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.229+2464_229+2468d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
C | CTTTTTCT others(2): Show |
11 | a0001c0001t0008g0226a0001c0001t0008g0230a0001c0001t0010g0235others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.229+2444_229+2445i others(11): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
C | CTTTTTCT others(3): Show |
4 | a0001c0001t0008g0223a0001c0001t0008g0227a0001c0001t0008g0234others(1): Show | 4 | HG01433.hp1 HG02257.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+2444_229+2445i others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
C | CTTTTTCT others(4): Show |
3 | a0001c0001t0010g0238a0001c0001t0028g0302a0001c0001t0041g0240 | 3 | HG01978.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.229+2444_229+2445i others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
C | CTTTTTCT others(5): Show |
1 | a0001c0001t0028g0303 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.229+2444_229+2445i others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
C | CTTTTTCT others(6): Show |
2 | a0001c0001t0010g0219a0001c0001t0010g0225 | 2 | NA18952.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.229+2444_229+2445i others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
C | CTTTTTT | 48 | a0001c0001t0002g0116a0001c0001t0002g0126a0001c0001t0002g0134others(45): Show | 48 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.229+2463_229+2468d others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
C | CTTTTTTT | 30 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0112others(27): Show | 30 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.229+2462_229+2468d others(9): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
C | CTTTTTTT others(1): Show |
19 | a0001c0001t0002g0111a0001c0001t0002g0128a0001c0001t0002g0141others(16): Show | 19 | HG00423.hp2 HG00438.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.229+2461_229+2468d others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0064g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.229+2459_229+2468d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0065g0103 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.229+2458_229+2468d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0007g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.229+2446_229+2468d others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
CT | C | 28 | a0001c0001t0003g0021a0001c0001t0003g0037a0001c0001t0009g0032others(25): Show | 28 | HG00099.hp2 HG00738.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.229+2468delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
CTT | C | 9 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0016g0087others(6): Show | 9 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.229+2467_229+2468d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0008g0222a0001c0001t0021g0015 | 2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.229+2459_229+2468d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685760
|
CTTTTTTT others(4): Show |
C | 12 | a0001c0001t0007g0008a0001c0001t0007g0009a0001c0001t0007g0012others(9): Show | 12 | HG01192.hp1 HG02615.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.229+2458_229+2468d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | |||||
| chr22:17685776
|
T | C | 1 | a0001c0001t0008g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.229+2455T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685776 | ||||||
| chr22:17685828
|
G | A | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.229+2507G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685828 | ||||||
| chr22:17685832
|
C | T | 2 | a0001c0001t0053g0139a0004c0006t0001g0090 | 2 | HG01081.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.229+2511C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685832 | ||||||
| chr22:17685857
|
C | T | 1 | a0001c0002t0001g0290 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.229+2536C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685857 | ||||||
| chr22:17685902
|
G | A | 1 | a0001c0001t0004g0246 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.229+2581G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685902 | ||||||
| chr22:17685937
|
C | A | 22 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(19): Show | 22 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.229+2616C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685937 | ||||||
| chr22:17685962
|
C | T | 7 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.229+2641C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685962 | ||||||
| chr22:17686008
|
A | G | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.229+2687A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686008 | ||||||
| chr22:17686010
|
G | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.229+2689G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686010 | ||||||
| chr22:17686100
|
A | G | 1 | a0001c0001t0004g0098 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.229+2779A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686100 | ||||||
| chr22:17686183
|
C | T | 1 | a0001c0001t0011g0151 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.230-2803C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686183 | ||||||
| chr22:17686224
|
G | A | 1 | a0001c0002t0014g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.230-2762G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686224 | ||||||
| chr22:17686237
|
C | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-2749C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686237 | ||||||
| chr22:17686246
|
T | G | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.230-2740T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686246 | ||||||
| chr22:17686446
|
T | A | 1 | a0001c0001t0003g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.230-2540T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686446 | ||||||
| chr22:17686446
|
T | G | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.230-2540T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686446 | ||||||
| chr22:17686455
|
T | A | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.230-2531T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686455 | ||||||
| chr22:17686503
|
ATTTCTTT others(3): Show |
A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-2469_230-2460d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17686503 | |||||
| chr22:17686517
|
C | CTT | 155 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(152): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.230-2459_230-2458d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17686517 | |||||
| chr22:17686517
|
C | T | 1 | a0001c0001t0003g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.230-2469C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686517 | ||||||
| chr22:17686518
|
T | C | 1 | a0001c0001t0003g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.230-2468T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686518 | ||||||
| chr22:17686657
|
C | G | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.230-2329C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686657 | ||||||
| chr22:17686743
|
T | C | 1 | a0001c0001t0034g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.230-2243T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686743 | ||||||
| chr22:17686756
|
G | A | 6 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0118others(3): Show | 6 | HG01255.hp2 HG02109.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.230-2230G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686756 | ||||||
| chr22:17686761
|
G | A | 1 | a0001c0001t0046g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.230-2225G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686761 | ||||||
| chr22:17686906
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.230-2080G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686906 | ||||||
| chr22:17686962
|
C | T | 1 | a0001c0001t0046g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.230-2024C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686962 | ||||||
| chr22:17687134
|
C | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.230-1852C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687134 | ||||||
| chr22:17687209
|
C | G | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.230-1777C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687209 | ||||||
| chr22:17687291
|
G | A | 2 | a0001c0001t0003g0057a0001c0001t0003g0058 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.230-1695G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687291 | ||||||
| chr22:17687317
|
GTTTTATT others(4): Show |
G | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.230-1660_230-1650d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17687317 | |||||
| chr22:17687360
|
GAGACAGA others(5): Show |
G | 1 | a0001c0001t0003g0021 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.230-1624_230-1613d others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17687360 | |||||
| chr22:17687390
|
G | A | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.230-1596G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687390 | ||||||
| chr22:17687441
|
A | G | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.230-1545A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687441 | ||||||
| chr22:17687538
|
C | A | 1 | a0001c0001t0062g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.230-1448C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687538 | ||||||
| chr22:17687586
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.230-1400G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687586 | ||||||
| chr22:17687612
|
G | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.230-1374G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687612 | ||||||
| chr22:17687678
|
A | G | 2 | a0001c0009t0004g0157a0001c0009t0004g0158 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.230-1308A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687678 | ||||||
| chr22:17687739
|
G | A | 1 | a0001c0002t0001g0258 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.230-1247G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687739 | ||||||
| chr22:17687818
|
C | A | 1 | a0001c0001t0003g0021 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.230-1168C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687818 | ||||||
| chr22:17687818
|
C | CT | 167 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(164): Show | 167 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.230-1152dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17687818 | |||||
| chr22:17687818
|
C | CTT | 9 | a0001c0001t0002g0176a0001c0001t0002g0245a0001c0001t0004g0155others(6): Show | 9 | HG01069.hp1 HG01934.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.230-1153_230-1152d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17687818 | |||||
| chr22:17687819
|
T | C | 7 | a0001c0001t0006g0070a0001c0002t0006g0071a0001c0002t0006g0078others(4): Show | 7 | HG02145.hp1 HG02280.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.230-1167T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687819 | ||||||
| chr22:17687979
|
G | A | 1 | a0001c0001t0010g0146 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.230-1007G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687979 | ||||||
| chr22:17688030
|
C | T | 7 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.230-956C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688030 | ||||||
| chr22:17688252
|
C | T | 2 | a0001c0001t0002g0203a0001c0001t0002g0213 | 2 | NA18964.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.230-734C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688252 | ||||||
| chr22:17688323
|
A | G | 12 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(9): Show | 12 | HG02572.hp2 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.230-663A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688323 | ||||||
| chr22:17688336
|
T | A | 1 | a0001c0001t0004g0136 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.230-650T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688336 | ||||||
| chr22:17688345
|
C | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.230-641C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688345 | ||||||
| chr22:17688457
|
A | T | 1 | a0001c0001t0005g0182 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.230-529A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688457 | ||||||
| chr22:17688534
|
A | G | 1 | a0001c0002t0001g0293 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.230-452A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688534 | ||||||
| chr22:17688535
|
T | A | 1 | a0001c0002t0001g0293 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.230-451T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688535 | ||||||
| chr22:17688646
|
A | G | 1 | a0001c0001t0005g0241 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.230-340A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688646 | ||||||
| chr22:17688722
|
G | A | 1 | a0001c0001t0054g0183 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.230-264G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688722 | ||||||
| chr22:17688762
|
A | G | 1 | a0001c0001t0004g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.230-224A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688762 | ||||||
| chr22:17688768
|
G | GT | 22 | a0001c0001t0002g0116a0001c0001t0002g0150a0001c0001t0003g0002others(19): Show | 22 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.230-202dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17688768 | |||||
| chr22:17688768
|
G | T | 2 | a0001c0002t0012g0305a0001c0002t0012g0306 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.230-218G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688768 | ||||||
| chr22:17688791
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-195G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688791 | ||||||
| chr22:17688801
|
C | T | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.230-185C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688801 | ||||||
| chr22:17688824
|
G | A | 22 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(19): Show | 22 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.230-162G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688824 | ||||||
| chr22:17688884
|
C | T | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.230-102C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688884 | ||||||
| chr22:17689328
|
G | A | 1 | a0001c0001t0003g0035 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.386+186G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689328 | ||||||
| chr22:17689421
|
C | G | 1 | a0002c0003t0001g0262 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.386+279C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689421 | ||||||
| chr22:17689470
|
C | G | 182 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(179): Show | 182 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.386+328C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689470 | ||||||
| chr22:17689571
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.386+429G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689571 | ||||||
| chr22:17689619
|
C | T | 1 | a0001c0001t0008g0230 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.386+477C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689619 | ||||||
| chr22:17689768
|
G | A | 162 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(159): Show | 162 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.386+626G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689768 | ||||||
| chr22:17689770
|
G | C | 1 | a0001c0001t0003g0021 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.386+628G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689770 | ||||||
| chr22:17689842
|
C | CA | 12 | a0001c0001t0002g0216a0001c0002t0001g0120a0001c0002t0001g0259others(9): Show | 12 | HG00544.hp2 HG01256.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.386+718dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17689842 | |||||
| chr22:17689842
|
CA | C | 208 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(205): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.386+718delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17689842 | |||||
| chr22:17689859
|
A | C | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.386+717A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689859 | ||||||
| chr22:17689860
|
A | C | 7 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.386+718A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689860 | ||||||
| chr22:17689863
|
C | A | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.386+721C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689863 | ||||||
| chr22:17689872
|
G | A | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.386+730G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689872 | ||||||
| chr22:17690091
|
C | T | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.386+949C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690091 | ||||||
| chr22:17690124
|
G | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.386+982G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690124 | ||||||
| chr22:17690200
|
C | T | 1 | a0001c0001t0046g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.386+1058C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690200 | ||||||
| chr22:17690241
|
G | A | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+1099G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690241 | ||||||
| chr22:17690329
|
G | GA | 156 | a0001c0001t0002g0099a0001c0001t0002g0111a0001c0001t0002g0112others(153): Show | 156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.386+1194dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17690329 | |||||
| chr22:17690337
|
T | A | 93 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0024others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.386+1195T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690337 | ||||||
| chr22:17690338
|
T | A | 44 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0034others(41): Show | 44 | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.386+1196T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690338 | ||||||
| chr22:17690339
|
T | A | 1 | a0001c0001t0003g0021 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.386+1197T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690339 | ||||||
| chr22:17690391
|
G | A | 1 | a0001c0001t0004g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.386+1249G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690391 | ||||||
| chr22:17690581
|
A | G | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+1439A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690581 | ||||||
| chr22:17690743
|
G | A | 29 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0034others(26): Show | 29 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.386+1601G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690743 | ||||||
| chr22:17690815
|
A | G | 1 | a0001c0001t0011g0180 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.386+1673A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690815 | ||||||
| chr22:17690920
|
A | G | 1 | a0002c0003t0001g0268 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.386+1778A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690920 | ||||||
| chr22:17690981
|
T | C | 13 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(10): Show | 13 | HG02572.hp2 HG02630.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.386+1839T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690981 | ||||||
| chr22:17691205
|
G | A | 1 | a0001c0001t0032g0166 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.386+2063G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691205 | ||||||
| chr22:17691224
|
A | G | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.386+2082A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691224 | ||||||
| chr22:17691336
|
G | A | 2 | a0001c0001t0002g0138a0001c0001t0002g0188 | 2 | HG00280.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.386+2194G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691336 | ||||||
| chr22:17691350
|
T | G | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.386+2208T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691350 | ||||||
| chr22:17691358
|
TTG | T | 182 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(179): Show | 182 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.386+2218_386+2219d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17691358 | |||||
| chr22:17691372
|
C | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.386+2230C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691372 | ||||||
| chr22:17691532
|
G | T | 2 | a0001c0001t0007g0248a0001c0001t0007g0249 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.386+2390G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691532 | ||||||
| chr22:17691585
|
G | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+2443G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691585 | ||||||
| chr22:17691595
|
G | A | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+2453G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691595 | ||||||
| chr22:17691612
|
C | T | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.386+2470C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691612 | ||||||
| chr22:17691651
|
C | CA | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.386+2519dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17691651 | |||||
| chr22:17691689
|
T | G | 1 | a0001c0001t0007g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.386+2547T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691689 | ||||||
| chr22:17691752
|
T | C | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+2610T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691752 | ||||||
| chr22:17691763
|
A | C | 7 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.386+2621A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691763 | ||||||
| chr22:17691765
|
A | G | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+2623A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691765 | ||||||
| chr22:17691819
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.386+2677C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691819 | ||||||
| chr22:17691868
|
A | AT | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.386+2729dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17691868 | |||||
| chr22:17691892
|
A | G | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.386+2750A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691892 | ||||||
| chr22:17691945
|
G | A | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.386+2803G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691945 | ||||||
| chr22:17692015
|
T | C | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.386+2873T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692015 | ||||||
| chr22:17692137
|
A | G | 1 | a0001c0001t0010g0238 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.386+2995A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692137 | ||||||
| chr22:17692230
|
A | G | 3 | a0001c0001t0002g0116a0001c0001t0002g0138a0001c0001t0002g0188 | 3 | HG00280.hp1 HG00639.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.386+3088A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692230 | ||||||
| chr22:17692264
|
A | G | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+3122A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692264 | ||||||
| chr22:17692605
|
T | C | 22 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.386+3463T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692605 | ||||||
| chr22:17692784
|
G | A | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.387-3357G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692784 | ||||||
| chr22:17692792
|
A | T | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.387-3349A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692792 | ||||||
| chr22:17692915
|
A | G | 7 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-3226A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692915 | ||||||
| chr22:17692954
|
G | A | 3 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0204 | 3 | HG03927.hp1 HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.387-3187G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692954 | ||||||
| chr22:17692964
|
C | T | 1 | a0001c0001t0055g0129 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.387-3177C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692964 | ||||||
| chr22:17693176
|
G | A | 1 | a0001c0001t0017g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.387-2965G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693176 | ||||||
| chr22:17693333
|
G | GTTTA | 16 | a0001c0001t0002g0168a0001c0001t0005g0242a0001c0001t0007g0008others(13): Show | 16 | HG00738.hp2 HG01192.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.387-2779_387-2776d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693333 | |||||
| chr22:17693333
|
GTTTA | G | 13 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0118others(10): Show | 13 | HG01255.hp2 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.387-2779_387-2776d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693333 | |||||
| chr22:17693333
|
GTTTATTT others(5): Show |
G | 16 | a0001c0001t0024g0243a0001c0001t0024g0244a0001c0002t0001g0124others(13): Show | 16 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.387-2787_387-2776d others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693333 | |||||
| chr22:17693343
|
T | G | 1 | a0005c0008t0019g0255 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.387-2798T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693343 | ||||||
| chr22:17693362
|
T | G | 44 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(41): Show | 44 | HG00140.hp2 HG01243.hp1 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.387-2779T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693362 | ||||||
| chr22:17693364
|
T | G | 44 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(41): Show | 44 | HG00140.hp2 HG01243.hp1 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.387-2777T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693364 | ||||||
| chr22:17693365
|
A | G | 2 | a0001c0001t0009g0032a0001c0001t0009g0040 | 2 | HG00733.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.387-2776A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693365 | ||||||
| chr22:17693365
|
A | T | 44 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(41): Show | 44 | HG00140.hp2 HG01243.hp1 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.387-2776A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693365 | ||||||
| chr22:17693365
|
AGTG | A | 3 | a0001c0002t0006g0073a0001c0002t0006g0079a0001c0002t0014g0064 | 3 | HG03710.hp2 NA19240.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.387-2775_387-2773d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693365 | ||||||
| chr22:17693365
|
AGTGTT | A | 16 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(13): Show | 16 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.387-2775_387-2771d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693365 | ||||||
| chr22:17693366
|
G | T | 44 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(41): Show | 44 | HG00140.hp2 HG01243.hp1 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.387-2775G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693366 | ||||||
| chr22:17693368
|
G | T | 2 | a0001c0001t0009g0032a0001c0001t0009g0040 | 2 | HG00733.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.387-2773G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693368 | ||||||
| chr22:17693368
|
GTTTGTTT others(3): Show |
G | 11 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(8): Show | 11 | HG00423.hp1 HG01109.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.387-2769_387-2760d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693368 | |||||
| chr22:17693368
|
GTTTGTTT others(6): Show |
G | 2 | a0001c0002t0006g0078a0004c0006t0001g0092 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.387-2769_387-2757d others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693368 | |||||
| chr22:17693368
|
GTTTGTTT others(7): Show |
G | 3 | a0004c0006t0001g0090a0004c0006t0049g0091a0004c0006t0063g0093 | 3 | HG02280.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.387-2769_387-2756d others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693368 | |||||
| chr22:17693372
|
G | A | 3 | a0001c0002t0006g0073a0001c0002t0006g0079a0001c0002t0014g0064 | 3 | HG03710.hp2 NA19240.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.387-2769G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693372 | ||||||
| chr22:17693372
|
G | GGTTT | 3 | a0001c0001t0003g0024a0001c0001t0003g0251a0007c0013t0003g0028 | 3 | HG02922.hp1 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.387-2769_387-2768i others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693372 | ||||||
| chr22:17693372
|
G | GGTTTT | 15 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0025others(12): Show | 15 | HG00140.hp2 HG01496.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.387-2769_387-2768i others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693372 | ||||||
| chr22:17693372
|
G | GGTTTTT | 25 | a0001c0001t0003g0002a0001c0001t0003g0030a0001c0001t0003g0034others(22): Show | 25 | HG01981.hp1 HG02135.hp2 HG02572.hp2 others(22): Show |
intron_variant | MODIFIER | c.387-2769_387-2768i others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693372 | ||||||
| chr22:17693372
|
G | GT | 11 | a0001c0001t0007g0249a0001c0002t0001g0095a0001c0002t0001g0123others(8): Show | 11 | HG00408.hp2 HG00639.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.387-2745dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693372 | |||||
| chr22:17693372
|
G | T | 24 | a0001c0001t0006g0070a0001c0001t0009g0032a0001c0001t0009g0040others(21): Show | 24 | HG00099.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.387-2769G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693372 | ||||||
| chr22:17693372
|
GT | G | 54 | a0001c0001t0002g0099a0001c0001t0002g0112a0001c0001t0002g0116others(51): Show | 54 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.387-2745delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693372 | |||||
| chr22:17693372
|
GTT | G | 97 | a0001c0001t0002g0100a0001c0001t0002g0111a0001c0001t0002g0138others(94): Show | 97 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.387-2746_387-2745d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693372 | |||||
| chr22:17693374
|
T | A | 16 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(13): Show | 16 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.387-2767T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693374 | ||||||
| chr22:17693374
|
T | G | 1 | a0001c0002t0052g0285 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.387-2767T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693374 | ||||||
| chr22:17693376
|
T | A | 3 | a0001c0002t0006g0073a0001c0002t0006g0079a0001c0002t0014g0064 | 3 | HG03710.hp2 NA19240.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.387-2765T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693376 | ||||||
| chr22:17693377
|
T | A | 1 | a0001c0002t0037g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.387-2764T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693377 | ||||||
| chr22:17693377
|
T | G | 2 | a0001c0001t0022g0237a0001c0001t0022g0239 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.387-2764T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693377 | ||||||
| chr22:17693378
|
T | A | 16 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(13): Show | 16 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.387-2763T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693378 | ||||||
| chr22:17693378
|
T | G | 20 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(17): Show | 20 | HG01433.hp1 HG01978.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.387-2763T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693378 | ||||||
| chr22:17693379
|
T | G | 16 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(13): Show | 16 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.387-2762T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693379 | ||||||
| chr22:17693379
|
T | TAG | 3 | a0001c0002t0006g0073a0001c0002t0006g0079a0001c0002t0014g0064 | 3 | HG03710.hp2 NA19240.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.387-2762_387-2761i others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693379 | ||||||
| chr22:17693380
|
T | G | 1 | a0001c0002t0037g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.387-2761T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693380 | ||||||
| chr22:17693381
|
T | G | 19 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(16): Show | 19 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.387-2760T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693381 | ||||||
| chr22:17693384
|
T | G | 1 | a0001c0001t0034g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.387-2757T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693384 | ||||||
| chr22:17693526
|
T | C | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-2615T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693526 | ||||||
| chr22:17693646
|
C | G | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.387-2495C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693646 | ||||||
| chr22:17693670
|
G | T | 1 | a0006c0010t0001g0263 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.387-2471G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693670 | ||||||
| chr22:17694033
|
C | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-2108C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694033 | ||||||
| chr22:17694098
|
G | A | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.387-2043G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694098 | ||||||
| chr22:17694147
|
T | A | 27 | a0001c0001t0006g0070a0001c0001t0029g0174a0001c0002t0006g0066others(24): Show | 27 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.387-1994T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694147 | ||||||
| chr22:17694326
|
A | G | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.387-1815A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694326 | ||||||
| chr22:17694382
|
T | C | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.387-1759T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694382 | ||||||
| chr22:17694506
|
TA | T | 55 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(52): Show | 55 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.387-1624delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17694506 | |||||
| chr22:17694517
|
A | T | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.387-1624A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694517 | ||||||
| chr22:17694518
|
T | A | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.387-1623T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694518 | ||||||
| chr22:17694553
|
C | T | 7 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-1588C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694553 | ||||||
| chr22:17694872
|
T | G | 1 | a0001c0001t0002g0215 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.387-1269T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694872 | ||||||
| chr22:17695011
|
G | A | 1 | a0001c0001t0007g0248 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.387-1130G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695011 | ||||||
| chr22:17695035
|
G | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1106G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695035 | ||||||
| chr22:17695036
|
GC | G | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1103delC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17695036 | |||||
| chr22:17695040
|
C | G | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1101C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695040 | ||||||
| chr22:17695042
|
T | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1099T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695042 | ||||||
| chr22:17695044
|
G | C | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1097G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695044 | ||||||
| chr22:17695045
|
C | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1096C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695045 | ||||||
| chr22:17695046
|
A | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1095A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695046 | ||||||
| chr22:17695049
|
G | GGTTCC | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1092_387-1091i others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695049 | ||||||
| chr22:17695050
|
C | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1091C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695050 | ||||||
| chr22:17695097
|
G | A | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.387-1044G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695097 | ||||||
| chr22:17695216
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.387-925C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695216 | ||||||
| chr22:17695341
|
G | A | 3 | a0001c0001t0008g0230a0001c0001t0010g0219a0001c0001t0010g0225 | 3 | NA18952.hp2 NA18956.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.387-800G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695341 | ||||||
| chr22:17695413
|
C | T | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.387-728C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695413 | ||||||
| chr22:17695531
|
A | C | 1 | a0001c0001t0003g0035 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.387-610A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695531 | ||||||
| chr22:17695571
|
C | T | 1 | a0001c0001t0062g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.387-570C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695571 | ||||||
| chr22:17695627
|
A | T | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.387-514A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695627 | ||||||
| chr22:17695682
|
A | C | 1 | a0003c0004t0015g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.387-459A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695682 | ||||||
| chr22:17695692
|
T | C | 2 | a0001c0001t0007g0248a0001c0001t0007g0249 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.387-449T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695692 | ||||||
| chr22:17695756
|
C | T | 7 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-385C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695756 | ||||||
| chr22:17695929
|
T | G | 1 | a0001c0001t0004g0097 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.387-212T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695929 | ||||||
| chr22:17695983
|
T | A | 1 | a0001c0001t0004g0097 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.387-158T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695983 | ||||||
| chr22:17696019
|
A | G | 2 | a0001c0002t0001g0264a0001c0002t0001g0265 | 2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.387-122A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17696019 | ||||||
| chr22:17696071
|
T | A | 1 | a0001c0001t0004g0097 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.387-70T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17696071 | ||||||
| chr22:17696093
|
C | T | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.387-48C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17696093 | ||||||
| chr22:17696334
|
T | C | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.456+124T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696334 | ||||||
| chr22:17696366
|
C | T | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.456+156C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696366 | ||||||
| chr22:17696367
|
G | A | 2 | a0001c0001t0003g0022a0001c0001t0003g0035 | 2 | NA18986.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.456+157G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696367 | ||||||
| chr22:17696449
|
C | G | 1 | a0001c0002t0027g0006 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.456+239C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696449 | ||||||
| chr22:17696623
|
G | A | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.456+413G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696623 | ||||||
| chr22:17696633
|
C | T | 72 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.456+423C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696633 | ||||||
| chr22:17696636
|
T | A | 1 | a0001c0001t0004g0097 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.456+426T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696636 | ||||||
| chr22:17696706
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+496G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696706 | ||||||
| chr22:17696847
|
G | T | 1 | a0001c0001t0003g0051 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.456+637G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696847 | ||||||
| chr22:17696883
|
G | T | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.456+673G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696883 | ||||||
| chr22:17696983
|
T | G | 1 | a0007c0013t0003g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.456+773T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696983 | ||||||
| chr22:17697137
|
T | TA | 19 | a0001c0001t0020g0224a0001c0001t0020g0231a0001c0001t0020g0233others(16): Show | 19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.456+942dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17697137 | |||||
| chr22:17697137
|
TA | T | 11 | a0001c0001t0002g0138a0001c0001t0002g0217a0001c0001t0003g0022others(8): Show | 11 | HG00323.hp1 HG00639.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.456+942delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17697137 | |||||
| chr22:17697475
|
G | A | 1 | a0001c0001t0007g0248 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.456+1265G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17697475 | ||||||
| chr22:17697631
|
A | G | 45 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(42): Show | 45 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.456+1421A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17697631 | ||||||
| chr22:17697801
|
G | C | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.456+1591G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17697801 | ||||||
| chr22:17697826
|
T | TTTTA | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+1632_456+1635d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17697826 | |||||
| chr22:17697846
|
T | A | 22 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.456+1636T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17697846 | ||||||
| chr22:17697932
|
G | A | 1 | a0001c0002t0037g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.456+1722G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17697932 | ||||||
| chr22:17698094
|
G | A | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.456+1884G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698094 | ||||||
| chr22:17698145
|
T | C | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.456+1935T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698145 | ||||||
| chr22:17698179
|
C | T | 1 | a0001c0002t0001g0282 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.456+1969C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698179 | ||||||
| chr22:17698368
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.456+2158G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698368 | ||||||
| chr22:17698487
|
A | C | 1 | a0001c0001t0013g0164 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.456+2277A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698487 | ||||||
| chr22:17698506
|
C | T | 5 | a0001c0001t0002g0116a0001c0001t0002g0138a0001c0001t0002g0188others(2): Show | 5 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(2): Show |
intron_variant | MODIFIER | c.456+2296C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698506 | ||||||
| chr22:17698507
|
G | A | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.456+2297G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698507 | ||||||
| chr22:17698511
|
A | G | 3 | a0001c0001t0008g0226a0001c0001t0008g0229a0001c0001t0038g0228 | 3 | HG03041.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.456+2301A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698511 | ||||||
| chr22:17698554
|
CT | C | 7 | a0001c0001t0003g0037a0004c0006t0001g0090a0004c0006t0001g0092others(4): Show | 7 | HG02280.hp2 HG02965.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.456+2346delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17698554 | |||||
| chr22:17698555
|
T | TA | 136 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.456+2345_456+2346i others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698555 | ||||||
| chr22:17698555
|
T | TAA | 42 | a0001c0001t0002g0150a0001c0001t0002g0156a0001c0001t0002g0169others(39): Show | 42 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.456+2345_456+2346i others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698555 | ||||||
| chr22:17698555
|
T | TAAA | 3 | a0001c0001t0004g0136a0001c0001t0013g0236a0003c0004t0016g0087 | 3 | HG01934.hp2 NA18957.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.456+2345_456+2346i others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698555 | ||||||
| chr22:17698556
|
T | A | 247 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.456+2346T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698556 | ||||||
| chr22:17698667
|
T | A | 2 | a0001c0001t0005g0059a0001c0001t0005g0060 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.456+2457T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698667 | ||||||
| chr22:17698725
|
T | G | 3 | a0001c0001t0002g0100a0001c0001t0002g0216a0001c0001t0002g0217 | 3 | NA18968.hp1 NA18974.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.456+2515T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698725 | ||||||
| chr22:17698855
|
T | C | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.456+2645T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698855 | ||||||
| chr22:17698979
|
A | G | 1 | a0001c0001t0018g0207 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.456+2769A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698979 | ||||||
| chr22:17699103
|
A | G | 94 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.456+2893A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699103 | ||||||
| chr22:17699218
|
T | G | 45 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(42): Show | 45 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.456+3008T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699218 | ||||||
| chr22:17699445
|
CAA | C | 22 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.457-2796_457-2795d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17699445 | |||||
| chr22:17699542
|
A | G | 1 | a0001c0001t0007g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.457-2701A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699542 | ||||||
| chr22:17699588
|
A | G | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.457-2655A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699588 | ||||||
| chr22:17699595
|
G | A | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.457-2648G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699595 | ||||||
| chr22:17699811
|
T | C | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.457-2432T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699811 | ||||||
| chr22:17699889
|
T | C | 1 | a0005c0008t0019g0256 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.457-2354T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699889 | ||||||
| chr22:17699890
|
C | T | 3 | a0001c0002t0001g0264a0001c0002t0001g0265a0001c0002t0001g0290 | 3 | HG02683.hp2 HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.457-2353C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699890 | ||||||
| chr22:17700055
|
T | A | 1 | a0001c0001t0004g0097 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.457-2188T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700055 | ||||||
| chr22:17700073
|
A | G | 2 | a0002c0003t0001g0279a0002c0003t0001g0280 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.457-2170A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700073 | ||||||
| chr22:17700321
|
G | T | 2 | a0002c0003t0001g0220a0002c0003t0001g0221 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.457-1922G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700321 | ||||||
| chr22:17700326
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.457-1917A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700326 | ||||||
| chr22:17700737
|
G | C | 1 | a0001c0001t0053g0139 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.457-1506G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700737 | ||||||
| chr22:17700857
|
G | C | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.457-1386G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700857 | ||||||
| chr22:17700908
|
T | C | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.457-1335T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700908 | ||||||
| chr22:17700958
|
G | T | 12 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(9): Show | 12 | HG02572.hp2 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.457-1285G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700958 | ||||||
| chr22:17701018
|
A | G | 1 | a0001c0001t0004g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.457-1225A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701018 | ||||||
| chr22:17701245
|
G | A | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.457-998G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701245 | ||||||
| chr22:17701268
|
A | C | 1 | a0001c0001t0010g0225 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.457-975A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701268 | ||||||
| chr22:17701403
|
C | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.457-840C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701403 | ||||||
| chr22:17701404
|
G | A | 1 | a0001c0001t0013g0165 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.457-839G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701404 | ||||||
| chr22:17701447
|
A | G | 1 | a0001c0002t0027g0006 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.457-796A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701447 | ||||||
| chr22:17701482
|
A | G | 1 | a0001c0001t0011g0113 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.457-761A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701482 | ||||||
| chr22:17701524
|
T | C | 257 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.457-719T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701524 | ||||||
| chr22:17701529
|
T | C | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.457-714T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701529 | ||||||
| chr22:17701757
|
C | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.457-486C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701757 | ||||||
| chr22:17701851
|
G | T | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.457-392G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701851 | ||||||
| chr22:17701863
|
G | A | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.457-380G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701863 | ||||||
| chr22:17701882
|
C | T | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.457-361C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701882 | ||||||
| chr22:17701915
|
C | CAA | 44 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(41): Show | 44 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.457-311_457-310dup others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17701915 | |||||
| chr22:17701915
|
CA | C | 168 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(165): Show | 168 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.457-310delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17701915 | |||||
| chr22:17701915
|
CAA | C | 6 | a0001c0001t0005g0161a0001c0001t0005g0241a0001c0001t0028g0302others(3): Show | 6 | HG00408.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.457-311_457-310del others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17701915 | |||||
| chr22:17702075
|
C | G | 3 | a0001c0001t0008g0226a0001c0001t0008g0229a0001c0001t0038g0228 | 3 | HG03041.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.457-168C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17702075 | ||||||
| chr22:17702592
|
A | G | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+206A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17702592 | ||||||
| chr22:17702803
|
G | A | 2 | a0001c0001t0022g0237a0001c0001t0022g0239 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.600+417G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17702803 | ||||||
| chr22:17702953
|
G | T | 3 | a0001c0001t0008g0226a0001c0001t0008g0229a0001c0001t0038g0228 | 3 | HG03041.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.600+567G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17702953 | ||||||
| chr22:17703032
|
G | A | 1 | a0001c0002t0006g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.600+646G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703032 | ||||||
| chr22:17703053
|
G | A | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+667G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703053 | ||||||
| chr22:17703162
|
AAT | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.600+786_600+787del others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703162 | |||||
| chr22:17703168
|
T | TACACACA others(7): Show |
3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+783_600+784ins others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703168 | |||||
| chr22:17703168
|
T | TACACACA others(9): Show |
4 | a0001c0002t0012g0003a0001c0002t0012g0305a0001c0002t0012g0306others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+783_600+784ins others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703168 | |||||
| chr22:17703168
|
T | TACACACA others(11): Show |
1 | a0001c0002t0012g0004 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.600+783_600+784ins others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703168 | |||||
| chr22:17703170
|
T | C | 12 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.600+784T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703170 | ||||||
| chr22:17703172
|
T | C | 15 | a0001c0001t0003g0021a0001c0001t0003g0049a0001c0001t0003g0055others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.600+786T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703172 | ||||||
| chr22:17703172
|
T | TACACACA others(5): Show |
18 | a0001c0001t0006g0070a0001c0001t0024g0243a0001c0001t0024g0244others(15): Show | 18 | HG00099.hp2 HG00738.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.600+792_600+803dup others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703172 | |||||
| chr22:17703172
|
T | TACACACA others(7): Show |
5 | a0001c0002t0006g0068a0001c0002t0006g0069a0001c0002t0006g0073others(2): Show | 5 | HG01261.hp2 HG02071.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.600+790_600+803dup others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703172 | |||||
| chr22:17703190
|
T | C | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+804T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703190 | ||||||
| chr22:17703191
|
ATG | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+807_600+808del others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703191 | |||||
| chr22:17703194
|
T | C | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+808T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703194 | ||||||
| chr22:17703355
|
A | G | 2 | a0001c0001t0002g0196a0001c0001t0002g0210 | 2 | HG01074.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.600+969A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703355 | ||||||
| chr22:17703413
|
G | A | 23 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(20): Show | 23 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.600+1027G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703413 | ||||||
| chr22:17703475
|
C | CTCTT | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+1099_600+1102d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703475 | |||||
| chr22:17703683
|
C | T | 3 | a0001c0007t0009g0053a0001c0007t0009g0056a0001c0007t0044g0052 | 3 | HG03130.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.600+1297C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703683 | ||||||
| chr22:17703919
|
A | G | 2 | a0001c0002t0001g0286a0001c0002t0001g0297 | 2 | HG00741.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.600+1533A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703919 | ||||||
| chr22:17704039
|
C | T | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.600+1653C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704039 | ||||||
| chr22:17704257
|
T | C | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+1871T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704257 | ||||||
| chr22:17704282
|
C | T | 1 | a0001c0001t0046g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.600+1896C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704282 | ||||||
| chr22:17704431
|
A | G | 1 | a0001c0001t0002g0215 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.600+2045A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704431 | ||||||
| chr22:17704450
|
C | T | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+2064C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704450 | ||||||
| chr22:17704464
|
C | T | 1 | a0001c0001t0023g0105 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.600+2078C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704464 | ||||||
| chr22:17704551
|
G | A | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.600+2165G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704551 | ||||||
| chr22:17704563
|
G | A | 1 | a0006c0010t0001g0263 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.600+2177G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704563 | ||||||
| chr22:17704670
|
GT | G | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+2285delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704670 | ||||||
| chr22:17704987
|
C | CA | 7 | a0001c0001t0005g0007a0001c0001t0007g0108a0001c0001t0007g0109others(4): Show | 7 | HG01255.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+2615dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17704987 | |||||
| chr22:17704987
|
CA | C | 33 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(30): Show | 33 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.600+2615delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17704987 | |||||
| chr22:17705113
|
T | TA | 149 | a0001c0001t0002g0099a0001c0001t0002g0111a0001c0001t0002g0112others(146): Show | 149 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.600+2737dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17705113 | |||||
| chr22:17705113
|
TA | T | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.600+2737delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17705113 | |||||
| chr22:17705127
|
T | C | 1 | a0001c0002t0027g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.600+2741T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17705127 | ||||||
| chr22:17705300
|
AT | A | 24 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(21): Show | 24 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.600+2929delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17705300 | |||||
| chr22:17705699
|
C | T | 1 | a0001c0001t0018g0171 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.600+3313C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17705699 | ||||||
| chr22:17705703
|
T | A | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+3317T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17705703 | ||||||
| chr22:17705759
|
T | C | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+3373T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17705759 | ||||||
| chr22:17705784
|
C | T | 1 | a0001c0001t0006g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.600+3398C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17705784 | ||||||
| chr22:17706058
|
G | A | 1 | a0001c0001t0007g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.600+3672G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706058 | ||||||
| chr22:17706135
|
C | G | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.600+3749C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706135 | ||||||
| chr22:17706158
|
G | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.600+3772G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706158 | ||||||
| chr22:17706210
|
A | G | 1 | a0001c0001t0039g0160 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.600+3824A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706210 | ||||||
| chr22:17706223
|
T | C | 136 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(133): Show | 136 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.600+3837T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706223 | ||||||
| chr22:17706279
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+3893G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706279 | ||||||
| chr22:17706329
|
GT | G | 9 | a0001c0001t0003g0024a0001c0001t0003g0027a0001c0001t0003g0029others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+3958delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17706329 | |||||
| chr22:17706414
|
C | G | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+4028C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706414 | ||||||
| chr22:17706530
|
T | C | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+4144T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706530 | ||||||
| chr22:17706584
|
G | A | 6 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0118others(3): Show | 6 | HG01255.hp2 HG02109.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+4198G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706584 | ||||||
| chr22:17706703
|
G | A | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.600+4317G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706703 | ||||||
| chr22:17706751
|
T | C | 1 | a0001c0001t0011g0151 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.600+4365T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706751 | ||||||
| chr22:17706778
|
G | A | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.600+4392G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706778 | ||||||
| chr22:17706998
|
A | G | 3 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0048g0140 | 3 | HG01070.hp1 HG01071.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.600+4612A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706998 | ||||||
| chr22:17707181
|
GA | G | 94 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.600+4799delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17707181 | |||||
| chr22:17707259
|
C | T | 2 | a0001c0002t0012g0305a0001c0002t0012g0306 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.600+4873C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17707259 | ||||||
| chr22:17707359
|
G | A | 1 | a0001c0002t0037g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.600+4973G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17707359 | ||||||
| chr22:17707397
|
G | A | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+5011G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17707397 | ||||||
| chr22:17707548
|
T | C | 4 | a0001c0002t0014g0061a0001c0002t0014g0063a0001c0002t0014g0064others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+5162T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17707548 | ||||||
| chr22:17707623
|
G | A | 2 | a0001c0001t0022g0237a0001c0001t0022g0239 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.600+5237G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17707623 | ||||||
| chr22:17708011
|
G | A | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.600+5625G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17708011 | ||||||
| chr22:17708323
|
A | G | 1 | a0001c0002t0014g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.600+5937A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17708323 | ||||||
| chr22:17708329
|
T | C | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+5943T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17708329 | ||||||
| chr22:17708654
|
C | T | 1 | a0001c0001t0004g0098 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.600+6268C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17708654 | ||||||
| chr22:17709062
|
C | T | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+6676C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709062 | ||||||
| chr22:17709152
|
C | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.600+6766C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709152 | ||||||
| chr22:17709185
|
A | G | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.600+6799A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709185 | ||||||
| chr22:17709305
|
A | G | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+6919A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709305 | ||||||
| chr22:17709370
|
A | G | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.600+6984A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709370 | ||||||
| chr22:17709385
|
C | T | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.600+6999C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709385 | ||||||
| chr22:17709641
|
C | G | 3 | a0001c0007t0009g0053a0001c0007t0009g0056a0001c0007t0044g0052 | 3 | HG03130.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.600+7255C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709641 | ||||||
| chr22:17709750
|
C | G | 7 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+7364C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709750 | ||||||
| chr22:17709767
|
G | A | 5 | a0001c0001t0003g0021a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | NA18963.hp2 NA18974.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+7381G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709767 | ||||||
| chr22:17710053
|
G | A | 1 | a0001c0002t0001g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.600+7667G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710053 | ||||||
| chr22:17710067
|
T | TA | 40 | a0001c0001t0002g0111a0001c0001t0002g0141a0001c0001t0002g0154others(37): Show | 40 | HG01070.hp1 HG01109.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.600+7706dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17710067 | |||||
| chr22:17710067
|
T | TAA | 133 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0112others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.600+7705_600+7706d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17710067 | |||||
| chr22:17710067
|
T | TAAA | 16 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0203others(13): Show | 16 | HG00738.hp2 HG01192.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.600+7704_600+7706d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17710067 | |||||
| chr22:17710067
|
TA | T | 45 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(42): Show | 45 | HG00140.hp2 HG00733.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.600+7706delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17710067 | |||||
| chr22:17710067
|
TAAAAAAA others(5): Show |
T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.600+7695_600+7706d others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17710067 | |||||
| chr22:17710302
|
C | T | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.600+7916C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710302 | ||||||
| chr22:17710350
|
G | A | 16 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(13): Show | 16 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.600+7964G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710350 | ||||||
| chr22:17710395
|
T | C | 1 | a0001c0001t0007g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.600+8009T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710395 | ||||||
| chr22:17710433
|
C | A | 2 | a0001c0001t0005g0059a0001c0001t0005g0060 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.600+8047C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710433 | ||||||
| chr22:17710448
|
C | T | 1 | a0001c0002t0012g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.600+8062C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710448 | ||||||
| chr22:17710449
|
G | A | 1 | a0004c0006t0001g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.600+8063G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710449 | ||||||
| chr22:17710454
|
C | G | 1 | a0001c0002t0006g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.600+8068C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710454 | ||||||
| chr22:17710474
|
G | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.600+8088G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710474 | ||||||
| chr22:17710520
|
C | T | 1 | a0001c0002t0001g0264 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.600+8134C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710520 | ||||||
| chr22:17710540
|
A | T | 13 | a0001c0001t0007g0008a0001c0001t0007g0009a0001c0001t0007g0012others(10): Show | 13 | HG01192.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.600+8154A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710540 | ||||||
| chr22:17710583
|
A | G | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.600+8197A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710583 | ||||||
| chr22:17710615
|
G | A | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.600+8229G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710615 | ||||||
| chr22:17710642
|
C | A | 3 | a0001c0001t0008g0226a0001c0001t0008g0229a0001c0001t0038g0228 | 3 | HG03041.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.600+8256C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710642 | ||||||
| chr22:17710656
|
C | T | 1 | a0001c0001t0004g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.600+8270C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710656 | ||||||
| chr22:17710753
|
C | T | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.600+8367C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710753 | ||||||
| chr22:17710794
|
A | G | 253 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.600+8408A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710794 | ||||||
| chr22:17710824
|
T | C | 1 | a0001c0002t0014g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.600+8438T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710824 | ||||||
| chr22:17710872
|
G | A | 1 | a0001c0001t0002g0209 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.600+8486G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710872 | ||||||
| chr22:17710897
|
A | T | 6 | a0001c0007t0009g0053a0001c0007t0009g0056a0001c0007t0044g0052others(3): Show | 6 | HG02965.hp2 HG03130.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+8511A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710897 | ||||||
| chr22:17710901
|
T | A | 15 | a0001c0001t0002g0176a0002c0003t0001g0262a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG00733.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.600+8515T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710901 | ||||||
| chr22:17710941
|
C | T | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+8555C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710941 | ||||||
| chr22:17710984
|
G | A | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.600+8598G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710984 | ||||||
| chr22:17711066
|
A | T | 1 | a0001c0002t0027g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.600+8680A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711066 | ||||||
| chr22:17711067
|
A | T | 1 | a0001c0002t0027g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.600+8681A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711067 | ||||||
| chr22:17711304
|
C | CCTTTTTT others(7): Show |
1 | a0001c0001t0003g0048 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.600+8918_600+8919i others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711304 | ||||||
| chr22:17711304
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0003g0031 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.600+8919_600+8929d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | |||||
| chr22:17711304
|
C | CTTTTTTT others(5): Show |
36 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(33): Show | 36 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.600+8929_600+8930i others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | |||||
| chr22:17711304
|
C | CTTTTTTT others(6): Show |
13 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0041others(10): Show | 13 | HG01243.hp1 HG01496.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.600+8929_600+8930i others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | |||||
| chr22:17711304
|
C | CTTTTTTT others(7): Show |
24 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(21): Show | 24 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.600+8929_600+8930i others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | |||||
| chr22:17711304
|
C | CTTTTTTT others(8): Show |
14 | a0001c0002t0006g0079a0001c0002t0012g0305a0003c0004t0015g0080others(11): Show | 14 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.600+8929_600+8930i others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | |||||
| chr22:17711304
|
C | CTTTTTTT others(9): Show |
4 | a0003c0004t0016g0087a0003c0004t0016g0089a0003c0005t0006g0082others(1): Show | 4 | HG00423.hp1 HG01361.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+8929_600+8930i others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | |||||
| chr22:17711304
|
C | CTTTTTTT others(10): Show |
1 | a0003c0004t0030g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.600+8929_600+8930i others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | |||||
| chr22:17711344
|
C | T | 2 | a0001c0001t0022g0237a0001c0001t0022g0239 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.600+8958C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711344 | ||||||
| chr22:17711422
|
T | C | 95 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.600+9036T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711422 | ||||||
| chr22:17711604
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.600+9218G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711604 | ||||||
| chr22:17711848
|
T | G | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+9462T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711848 | ||||||
| chr22:17711898
|
A | G | 1 | a0001c0001t0003g0047 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.600+9512A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711898 | ||||||
| chr22:17712024
|
G | GT | 9 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0004g0201others(6): Show | 9 | HG02683.hp1 HG02738.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+9650dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17712024 | |||||
| chr22:17712305
|
C | T | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.600+9919C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17712305 | ||||||
| chr22:17712339
|
A | G | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.600+9953A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17712339 | ||||||
| chr22:17712792
|
T | C | 1 | a0001c0001t0007g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.600+10406T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17712792 | ||||||
| chr22:17712817
|
T | G | 4 | a0001c0001t0004g0163a0001c0001t0013g0164a0001c0001t0013g0165others(1): Show | 4 | HG02132.hp2 NA18943.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+10431T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17712817 | ||||||
| chr22:17712922
|
C | T | 3 | a0001c0001t0003g0054a0001c0001t0009g0032a0001c0001t0009g0040 | 3 | HG00733.hp1 HG01168.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.600+10536C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17712922 | ||||||
| chr22:17712994
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+10608G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17712994 | ||||||
| chr22:17713039
|
C | T | 1 | a0006c0010t0001g0263 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.600+10653C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713039 | ||||||
| chr22:17713238
|
A | G | 3 | a0001c0002t0026g0299a0001c0002t0026g0300a0001c0002t0035g0301 | 3 | HG02258.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.600+10852A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713238 | ||||||
| chr22:17713240
|
A | G | 1 | a0001c0001t0011g0133 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.600+10854A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713240 | ||||||
| chr22:17713282
|
G | C | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+10896G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713282 | ||||||
| chr22:17713310
|
A | G | 2 | a0001c0001t0005g0117a0001c0001t0005g0179 | 2 | NA18956.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.600+10924A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713310 | ||||||
| chr22:17713359
|
T | C | 1 | a0001c0001t0046g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.600+10973T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713359 | ||||||
| chr22:17713362
|
T | G | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.600+10976T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713362 | ||||||
| chr22:17713460
|
A | AT | 140 | a0001c0001t0002g0099a0001c0001t0002g0111a0001c0001t0002g0112others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.600+11092dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17713460 | |||||
| chr22:17713460
|
A | ATT | 20 | a0001c0001t0002g0150a0001c0001t0002g0199a0001c0001t0002g0204others(17): Show | 20 | HG00408.hp1 HG00438.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.600+11091_600+1109 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17713460 | |||||
| chr22:17713460
|
AT | A | 58 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(55): Show | 58 | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.600+11092delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17713460 | |||||
| chr22:17713460
|
ATT | A | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+11091_600+1109 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17713460 | |||||
| chr22:17713473
|
T | G | 19 | a0002c0003t0001g0220a0002c0003t0001g0221a0002c0003t0001g0262others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.600+11087T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713473 | ||||||
| chr22:17713500
|
C | T | 1 | a0001c0001t0005g0190 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.600+11114C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713500 | ||||||
| chr22:17713571
|
C | G | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+11185C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713571 | ||||||
| chr22:17713740
|
A | G | 1 | a0001c0001t0041g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.600+11354A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713740 | ||||||
| chr22:17713752
|
G | A | 1 | a0002c0003t0001g0262 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.600+11366G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713752 | ||||||
| chr22:17713913
|
G | A | 1 | a0001c0001t0046g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.600+11527G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713913 | ||||||
| chr22:17713993
|
A | T | 4 | a0001c0002t0014g0065a0001c0007t0009g0053a0001c0007t0009g0056others(1): Show | 4 | HG02717.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+11607A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713993 | ||||||
| chr22:17714019
|
C | T | 3 | a0001c0002t0026g0299a0001c0002t0026g0300a0001c0002t0035g0301 | 3 | HG02258.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.600+11633C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714019 | ||||||
| chr22:17714020
|
G | A | 1 | a0001c0001t0007g0127 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.600+11634G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714020 | ||||||
| chr22:17714060
|
G | A | 3 | a0001c0001t0008g0226a0001c0001t0008g0229a0001c0001t0038g0228 | 3 | HG03041.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.600+11674G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714060 | ||||||
| chr22:17714065
|
A | G | 47 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(44): Show | 47 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.600+11679A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714065 | ||||||
| chr22:17714109
|
T | C | 94 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.600+11723T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714109 | ||||||
| chr22:17714147
|
G | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+11761G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714147 | ||||||
| chr22:17714157
|
G | A | 12 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(9): Show | 12 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.600+11771G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714157 | ||||||
| chr22:17714287
|
C | T | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+11901C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714287 | ||||||
| chr22:17714346
|
G | A | 1 | a0001c0001t0047g0135 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.600+11960G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714346 | ||||||
| chr22:17714366
|
C | T | 1 | a0001c0001t0007g0248 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.600+11980C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714366 | ||||||
| chr22:17714395
|
C | T | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+12009C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714395 | ||||||
| chr22:17714406
|
G | C | 253 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.600+12020G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714406 | ||||||
| chr22:17714406
|
G | T | 1 | a0001c0001t0003g0002 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.600+12020G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714406 | ||||||
| chr22:17714412
|
A | G | 2 | a0001c0001t0003g0041a0001c0001t0003g0042 | 2 | NA18955.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.600+12026A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714412 | ||||||
| chr22:17714434
|
A | C | 1 | a0001c0001t0046g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.600+12048A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714434 | ||||||
| chr22:17714497
|
A | G | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+12111A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714497 | ||||||
| chr22:17714571
|
G | A | 1 | a0001c0001t0005g0173 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.601-12106G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714571 | ||||||
| chr22:17714590
|
C | T | 1 | a0001c0001t0046g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.601-12087C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714590 | ||||||
| chr22:17714858
|
A | G | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-11819A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714858 | ||||||
| chr22:17714970
|
G | A | 1 | a0001c0001t0005g0218 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.601-11707G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714970 | ||||||
| chr22:17715121
|
TTTATATA others(8): Show |
T | 1 | a0001c0001t0010g0235 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.601-11554_601-1154 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715121 | |||||
| chr22:17715122
|
T | A | 1 | a0001c0001t0003g0002 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.601-11555T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715122 | ||||||
| chr22:17715122
|
T | TTATATAT others(3): Show |
1 | a0002c0003t0001g0278 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.601-11515_601-1150 others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | |||||
| chr22:17715122
|
T | TTATATAT others(5): Show |
1 | a0002c0003t0001g0272 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.601-11517_601-1150 others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | |||||
| chr22:17715122
|
T | TTATATAT others(11): Show |
1 | a0001c0002t0001g0258 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.601-11523_601-1150 others(22): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | |||||
| chr22:17715122
|
T | TTATATAT others(13): Show |
1 | a0001c0002t0001g0283 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.601-11525_601-1150 others(24): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | |||||
| chr22:17715122
|
T | TTATATAT others(19): Show |
1 | a0001c0002t0001g0288 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.601-11531_601-1150 others(30): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | |||||
| chr22:17715122
|
TTATATAT others(3): Show |
T | 1 | a0001c0001t0046g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.601-11515_601-1150 others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | |||||
| chr22:17715122
|
TTATATAT others(7): Show |
T | 1 | a0001c0002t0026g0299 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.601-11519_601-1150 others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | |||||
| chr22:17715122
|
TTATATAT others(13): Show |
T | 2 | a0001c0001t0003g0036a0001c0001t0010g0219 | 2 | HG02135.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.601-11525_601-1150 others(24): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | |||||
| chr22:17715122
|
TTATATAT others(15): Show |
T | 3 | a0001c0001t0010g0225a0004c0006t0001g0092a0007c0013t0003g0028 | 3 | HG02922.hp1 HG03516.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.601-11527_601-1150 others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | |||||
| chr22:17715122
|
TTATATAT others(17): Show |
T | 2 | a0001c0002t0035g0301a0001c0007t0044g0052 | 2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601-11529_601-1150 others(28): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | |||||
| chr22:17715122
|
TTATATAT others(19): Show |
T | 4 | a0001c0001t0002g0199a0001c0001t0002g0204a0001c0001t0032g0166others(1): Show | 4 | HG00423.hp2 HG03927.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-11531_601-1150 others(30): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | |||||
| chr22:17715122
|
TTATATAT others(21): Show |
T | 15 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0131others(12): Show | 15 | HG01109.hp1 HG01255.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.601-11533_601-1150 others(32): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | |||||
| chr22:17715122
|
TTATATAT others(23): Show |
T | 4 | a0001c0001t0005g0179a0001c0001t0007g0008a0001c0001t0007g0009others(1): Show | 4 | HG01256.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-11535_601-1150 others(34): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | |||||
| chr22:17715136
|
ATATATAT others(31): Show |
A | 1 | a0001c0001t0003g0024 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.601-11539_601-1150 others(42): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715136 | |||||
| chr22:17715140
|
ATATATAT others(34): Show |
A | 1 | a0001c0014t0007g0010 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.601-11535_601-1149 others(45): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715140 | |||||
| chr22:17715141
|
TATATATA others(18): Show |
T | 1 | a0001c0001t0004g0200 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.601-11535_601-1151 others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715141 | ||||||
| chr22:17715141
|
TATATATA others(20): Show |
T | 7 | a0001c0001t0004g0097a0001c0001t0004g0132a0001c0001t0004g0153others(4): Show | 7 | HG00438.hp1 HG02135.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-11535_601-1150 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715141 | ||||||
| chr22:17715141
|
TATATATA others(22): Show |
T | 2 | a0001c0001t0005g0117a0001c0001t0011g0180 | 2 | NA18979.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.601-11535_601-1150 others(33): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715141 | ||||||
| chr22:17715142
|
ATATATAT others(22): Show |
A | 2 | a0001c0001t0017g0013a0001c0001t0017g0019 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.601-11533_601-1150 others(33): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715142 | |||||
| chr22:17715143
|
TATATATA others(18): Show |
T | 2 | a0001c0001t0004g0201a0001c0007t0009g0056 | 2 | HG02738.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.601-11533_601-1150 others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715143 | ||||||
| chr22:17715143
|
TATATATA others(20): Show |
T | 6 | a0001c0001t0004g0098a0001c0001t0004g0155a0001c0001t0004g0177others(3): Show | 6 | HG01256.hp1 HG01258.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-11533_601-1150 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715143 | ||||||
| chr22:17715144
|
ATATATAT others(20): Show |
A | 9 | a0001c0001t0002g0162a0001c0001t0004g0136a0001c0001t0005g0190others(6): Show | 9 | HG00609.hp2 HG00738.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-11531_601-1150 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715144 | |||||
| chr22:17715144
|
ATATATAT others(21): Show |
A | 8 | a0001c0001t0004g0130a0001c0001t0004g0191a0001c0001t0005g0148others(5): Show | 8 | HG01516.hp1 HG02071.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-11531_601-1150 others(32): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715144 | |||||
| chr22:17715144
|
ATATATAT others(22): Show |
A | 3 | a0001c0001t0005g0143a0001c0001t0017g0020a0001c0001t0064g0304 | 3 | HG02109.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.601-11531_601-1150 others(33): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715144 | |||||
| chr22:17715144
|
ATATATAT others(23): Show |
A | 1 | a0001c0001t0007g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.601-11531_601-1150 others(34): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715144 | |||||
| chr22:17715144
|
ATATATAT others(28): Show |
A | 1 | a0005c0008t0019g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.601-11531_601-1149 others(39): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715144 | |||||
| chr22:17715145
|
TATATATA others(18): Show |
T | 1 | a0001c0007t0009g0053 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.601-11531_601-1150 others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715145 | ||||||
| chr22:17715146
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0002g0134 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.601-11529_601-1150 others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715146 | |||||
| chr22:17715146
|
ATATATAT others(19): Show |
A | 10 | a0001c0001t0002g0203a0001c0001t0002g0211a0001c0001t0002g0213others(7): Show | 10 | HG00438.hp2 HG00609.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-11529_601-1150 others(30): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715146 | |||||
| chr22:17715146
|
ATATATAT others(20): Show |
A | 25 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0144others(22): Show | 25 | HG00099.hp1 HG00544.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.601-11529_601-1150 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715146 | |||||
| chr22:17715146
|
ATATATAT others(21): Show |
A | 8 | a0001c0001t0002g0126a0001c0001t0005g0007a0001c0001t0007g0109others(5): Show | 8 | HG02559.hp1 HG02622.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-11529_601-1150 others(32): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715146 | |||||
| chr22:17715146
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0005g0149 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.601-11529_601-1150 others(33): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715146 | |||||
| chr22:17715146
|
ATATATAT others(27): Show |
A | 1 | a0001c0002t0012g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.601-11529_601-1149 others(38): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715146 | |||||
| chr22:17715148
|
ATATATAT others(16): Show |
A | 2 | a0001c0001t0005g0241a0003c0004t0031g0254 | 2 | HG00408.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.601-11527_601-1150 others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | |||||
| chr22:17715148
|
ATATATAT others(17): Show |
A | 4 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0045others(1): Show | 4 | HG01981.hp1 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-11527_601-1150 others(28): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | |||||
| chr22:17715148
|
ATATATAT others(18): Show |
A | 5 | a0001c0001t0004g0163a0001c0001t0047g0135a0002c0003t0001g0274others(2): Show | 5 | HG00323.hp1 HG01361.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-11527_601-1150 others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | |||||
| chr22:17715148
|
ATATATAT others(19): Show |
A | 4 | a0001c0001t0002g0100a0001c0001t0002g0150a0001c0001t0007g0108others(1): Show | 4 | HG03492.hp2 HG03831.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-11527_601-1150 others(30): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | |||||
| chr22:17715148
|
ATATATAT others(20): Show |
A | 7 | a0001c0001t0002g0138a0001c0001t0002g0154a0001c0001t0002g0188others(4): Show | 7 | HG00280.hp1 HG00639.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-11527_601-1150 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | |||||
| chr22:17715148
|
ATATATAT others(21): Show |
A | 2 | a0001c0001t0005g0182a0001c0001t0007g0118 | 2 | HG03017.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.601-11527_601-1150 others(32): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | |||||
| chr22:17715148
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0057g0125 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.601-11527_601-1149 others(33): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | |||||
| chr22:17715148
|
ATATATAT others(24): Show |
A | 1 | a0001c0001t0022g0239 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.601-11527_601-1149 others(35): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | |||||
| chr22:17715148
|
ATATATAT others(25): Show |
A | 1 | a0001c0001t0022g0237 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.601-11527_601-1149 others(36): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | |||||
| chr22:17715148
|
ATATATAT others(27): Show |
A | 2 | a0001c0002t0012g0305a0001c0002t0042g0005 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.601-11527_601-1149 others(38): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | |||||
| chr22:17715150
|
ATATATAT others(14): Show |
A | 3 | a0001c0001t0008g0227a0001c0001t0008g0230a0001c0001t0020g0224 | 3 | HG02698.hp2 HG02818.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.601-11525_601-1150 others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | |||||
| chr22:17715150
|
ATATATAT others(15): Show |
A | 4 | a0001c0001t0003g0051a0001c0001t0013g0164a0001c0001t0013g0236others(1): Show | 4 | NA18979.hp2 NA19077.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-11525_601-1150 others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | |||||
| chr22:17715150
|
ATATATAT others(16): Show |
A | 8 | a0001c0001t0003g0021a0001c0001t0003g0027a0001c0001t0003g0035others(5): Show | 8 | HG01109.hp2 HG03098.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-11525_601-1150 others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | |||||
| chr22:17715150
|
ATATATAT others(17): Show |
A | 20 | a0001c0001t0003g0029a0001c0001t0003g0034a0001c0001t0003g0037others(17): Show | 20 | HG00140.hp2 HG00733.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.601-11525_601-1150 others(28): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | |||||
| chr22:17715150
|
ATATATAT others(18): Show |
A | 6 | a0001c0001t0002g0209a0001c0001t0009g0032a0003c0004t0015g0080others(3): Show | 6 | HG01168.hp2 HG01175.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-11525_601-1150 others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | |||||
| chr22:17715150
|
ATATATAT others(19): Show |
A | 3 | a0001c0001t0002g0176a0001c0001t0008g0226a0003c0005t0006g0083 | 3 | HG00423.hp1 HG01069.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.601-11525_601-1150 others(30): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | |||||
| chr22:17715150
|
ATATATAT others(20): Show |
A | 2 | a0001c0001t0002g0147a0001c0001t0008g0229 | 2 | HG03041.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.601-11525_601-1149 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | |||||
| chr22:17715150
|
ATATATAT others(21): Show |
A | 2 | a0001c0001t0002g0210a0001c0001t0038g0228 | 2 | HG01175.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.601-11525_601-1149 others(32): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | |||||
| chr22:17715150
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0002g0196 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.601-11525_601-1149 others(33): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | |||||
| chr22:17715150
|
ATATATAT others(27): Show |
A | 1 | a0001c0002t0012g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.601-11525_601-1149 others(38): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | |||||
| chr22:17715152
|
ATATATAT others(13): Show |
A | 3 | a0001c0001t0002g0112a0001c0001t0008g0222a0001c0001t0010g0238 | 3 | HG01071.hp2 HG01978.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.601-11523_601-1150 others(24): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | |||||
| chr22:17715152
|
ATATATAT others(14): Show |
A | 4 | a0001c0001t0002g0111a0001c0001t0002g0128a0001c0001t0013g0165others(1): Show | 4 | HG01070.hp1 HG01070.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-11523_601-1150 others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | |||||
| chr22:17715152
|
ATATATAT others(15): Show |
A | 4 | a0001c0001t0003g0026a0001c0001t0008g0234a0001c0001t0010g0146others(1): Show | 4 | HG01433.hp1 HG02647.hp2 NA19089.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-11523_601-1150 others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | |||||
| chr22:17715152
|
ATATATAT others(16): Show |
A | 2 | a0001c0001t0003g0002a0004c0006t0049g0091 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.601-11523_601-1150 others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | |||||
| chr22:17715152
|
ATATATAT others(17): Show |
A | 3 | a0001c0001t0003g0022a0001c0001t0003g0046a0001c0001t0003g0104 | 3 | HG04199.hp1 NA18967.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.601-11523_601-1150 others(28): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | |||||
| chr22:17715152
|
ATATATAT others(20): Show |
A | 2 | a0001c0001t0002g0141a0001c0001t0033g0137 | 2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.601-11523_601-1149 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | |||||
| chr22:17715152
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0002g0212 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.601-11523_601-1149 others(32): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | |||||
| chr22:17715152
|
ATATATAT others(23): Show |
A | 1 | a0001c0002t0012g0004 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601-11523_601-1149 others(34): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | |||||
| chr22:17715154
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0024g0243 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.601-11521_601-1150 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715154 | |||||
| chr22:17715154
|
ATATATAT others(14): Show |
A | 1 | a0001c0002t0006g0077 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.601-11521_601-1150 others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715154 | |||||
| chr22:17715154
|
ATATATAT others(15): Show |
A | 3 | a0001c0001t0003g0048a0001c0001t0003g0050a0001c0002t0027g0076 | 3 | HG02145.hp2 NA18974.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.601-11521_601-1150 others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715154 | |||||
| chr22:17715154
|
ATATATAT others(16): Show |
A | 5 | a0001c0001t0003g0025a0001c0001t0003g0251a0001c0001t0003g0252others(2): Show | 5 | HG00099.hp2 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-11521_601-1149 others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715154 | |||||
| chr22:17715154
|
ATATATAT others(17): Show |
A | 1 | a0001c0002t0027g0006 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.601-11521_601-1149 others(28): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715154 | |||||
| chr22:17715156
|
ATATATAT others(11): Show |
A | 2 | a0001c0001t0024g0244a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.601-11519_601-1150 others(22): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715156 | |||||
| chr22:17715156
|
ATATATAT others(12): Show |
A | 2 | a0001c0001t0041g0240a0001c0002t0037g0062 | 2 | HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.601-11519_601-1150 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715156 | |||||
| chr22:17715156
|
ATATATAT others(14): Show |
A | 2 | a0001c0001t0008g0223a0001c0002t0006g0073 | 2 | HG03710.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.601-11519_601-1149 others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715156 | |||||
| chr22:17715156
|
ATATATAT others(16): Show |
A | 3 | a0001c0002t0006g0066a0001c0002t0025g0074a0001c0002t0025g0075 | 3 | HG00738.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.601-11519_601-1149 others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715156 | |||||
| chr22:17715157
|
TATATATA others(6): Show |
T | 1 | a0001c0002t0026g0300 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.601-11519_601-1150 others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715157 | ||||||
| chr22:17715158
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0028g0302 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.601-11517_601-1150 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715158 | |||||
| chr22:17715158
|
ATATATAT others(14): Show |
A | 1 | a0004c0006t0001g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.601-11517_601-1149 others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715158 | |||||
| chr22:17715158
|
ATATATAT others(15): Show |
A | 2 | a0001c0002t0006g0068a0001c0002t0014g0065 | 2 | HG02602.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.601-11517_601-1149 others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715158 | |||||
| chr22:17715158
|
ATATATAT others(16): Show |
A | 2 | a0001c0002t0006g0067a0004c0006t0063g0093 | 2 | HG02280.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.601-11517_601-1149 others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715158 | |||||
| chr22:17715160
|
ATATATAT others(4): Show |
A | 1 | a0001c0002t0001g0281 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.601-11515_601-1150 others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715160 | |||||
| chr22:17715160
|
ATATATAT others(12): Show |
A | 2 | a0001c0002t0006g0069a0001c0002t0006g0079 | 2 | HG03654.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.601-11515_601-1149 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715160 | |||||
| chr22:17715160
|
ATATATAT others(13): Show |
A | 2 | a0001c0002t0014g0061a0001c0002t0014g0063 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.601-11515_601-1149 others(24): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715160 | |||||
| chr22:17715162
|
ATATATAT others(3): Show |
A | 1 | a0001c0002t0001g0261 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.601-11513_601-1150 others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715162 | |||||
| chr22:17715162
|
ATATATAT others(12): Show |
A | 1 | a0001c0002t0006g0072 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601-11513_601-1149 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715162 | |||||
| chr22:17715164
|
ATATATAT others(10): Show |
A | 1 | a0001c0002t0006g0078 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.601-11511_601-1149 others(21): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715164 | |||||
| chr22:17715168
|
A | T | 5 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0200others(2): Show | 5 | HG00735.hp2 HG02040.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-11509A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715168 | ||||||
| chr22:17715170
|
A | ATATATAT others(8): Show |
1 | a0002c0003t0059g0273 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.601-11506_601-1150 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715170
|
A | ATATATAT others(12): Show |
2 | a0001c0002t0001g0290a0001c0002t0069g0294 | 2 | HG00408.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.601-11506_601-1150 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715170
|
A | ATATATAT others(14): Show |
1 | a0001c0002t0052g0285 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.601-11506_601-1150 others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715170
|
A | ATATATAT others(11): Show |
1 | a0002c0003t0001g0270 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.601-11506_601-1150 others(22): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715170
|
A | ATATATAT others(15): Show |
1 | a0001c0002t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.601-11506_601-1150 others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715170
|
A | ATATATAT others(12): Show |
1 | a0002c0003t0058g0275 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.601-11506_601-1150 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715170
|
A | ATATATAT others(7): Show |
3 | a0002c0003t0001g0279a0002c0003t0001g0280a0002c0003t0001g0292 | 3 | HG01069.hp2 HG01071.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.601-11506_601-1150 others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715170
|
A | ATATATAT others(8): Show |
1 | a0006c0010t0001g0263 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601-11506_601-1150 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715170
|
A | ATATATAT others(5): Show |
1 | a0001c0002t0001g0289 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.601-11506_601-1150 others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715170
|
A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0259 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.601-11506_601-1150 others(21): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715170
|
A | ATATATAT others(4): Show |
2 | a0002c0003t0001g0266a0002c0003t0001g0267 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.601-11506_601-1150 others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715170
|
A | ATATATAT others(6): Show |
1 | a0001c0002t0001g0282 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.601-11506_601-1150 others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715170
|
A | T | 30 | a0001c0001t0004g0097a0001c0001t0004g0114a0001c0001t0004g0115others(27): Show | 30 | HG00423.hp2 HG00438.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.601-11507A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715170 | ||||||
| chr22:17715170
|
ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0006g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.601-11488_601-1147 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715170
|
ATTTTTTT others(10): Show |
A | 1 | a0001c0002t0006g0071 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.601-11490_601-1147 others(21): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | |||||
| chr22:17715171
|
T | TATATATA others(4): Show |
1 | a0002c0003t0001g0277 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.601-11506_601-1150 others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715171 | ||||||
| chr22:17715171
|
T | TATATATA others(12): Show |
1 | a0001c0002t0001g0265 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.601-11506_601-1150 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715171 | ||||||
| chr22:17715172
|
T | A | 2 | a0001c0002t0001g0283a0002c0003t0001g0278 | 2 | HG01981.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.601-11505T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715172 | ||||||
| chr22:17715173
|
T | A | 3 | a0001c0002t0001g0297a0002c0003t0001g0271a0002c0003t0001g0277 | 3 | HG00280.hp2 HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.601-11504T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715173 | ||||||
| chr22:17715174
|
T | A | 1 | a0002c0003t0001g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.601-11503T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715174 | ||||||
| chr22:17715227
|
G | GC | 5 | a0001c0001t0005g0143a0001c0001t0005g0145a0001c0001t0005g0149others(2): Show | 5 | HG01109.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-11449dupC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715227 | |||||
| chr22:17715331
|
G | A | 1 | a0001c0001t0004g0136 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.601-11346G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715331 | ||||||
| chr22:17715335
|
C | A | 1 | a0001c0002t0001g0283 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.601-11342C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715335 | ||||||
| chr22:17715343
|
G | A | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.601-11334G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715343 | ||||||
| chr22:17715500
|
C | T | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.601-11177C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715500 | ||||||
| chr22:17715561
|
C | G | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.601-11116C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715561 | ||||||
| chr22:17715980
|
T | A | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02040.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.601-10697T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715980 | ||||||
| chr22:17715992
|
A | T | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601-10685A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715992 | ||||||
| chr22:17716337
|
G | T | 3 | a0001c0007t0009g0053a0001c0007t0009g0056a0001c0007t0044g0052 | 3 | HG03130.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.601-10340G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17716337 | ||||||
| chr22:17716477
|
A | C | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-10200A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17716477 | ||||||
| chr22:17716717
|
A | G | 22 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.601-9960A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17716717 | ||||||
| chr22:17716779
|
T | G | 1 | a0001c0001t0050g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.601-9898T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17716779 | ||||||
| chr22:17717210
|
A | G | 94 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-9467A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717210 | ||||||
| chr22:17717283
|
C | T | 7 | a0001c0001t0004g0097a0001c0001t0004g0114a0001c0001t0004g0115others(4): Show | 7 | HG00423.hp2 HG02040.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-9394C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717283 | ||||||
| chr22:17717284
|
G | A | 94 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-9393G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717284 | ||||||
| chr22:17717354
|
TG | T | 94 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-9319delG | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717354 | |||||
| chr22:17717368
|
G | A | 1 | a0001c0001t0002g0212 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.601-9309G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717368 | ||||||
| chr22:17717380
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-9291_601-9290i others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | |||||
| chr22:17717380
|
C | CAAAAAAA others(9): Show |
12 | a0003c0004t0015g0080a0003c0004t0015g0253a0003c0004t0016g0087others(9): Show | 12 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.601-9291_601-9290i others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | |||||
| chr22:17717380
|
C | CAAAAAAA others(10): Show |
1 | a0003c0004t0015g0081 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.601-9291_601-9290i others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | |||||
| chr22:17717380
|
C | CAAAAAAA others(16): Show |
16 | a0001c0001t0006g0070a0001c0001t0009g0032a0001c0002t0006g0068others(13): Show | 16 | HG01168.hp2 HG01261.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.601-9291_601-9290i others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | |||||
| chr22:17717380
|
C | CAAAAAAA others(17): Show |
33 | a0001c0001t0003g0021a0001c0001t0003g0034a0001c0001t0003g0035others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.601-9291_601-9290i others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | |||||
| chr22:17717380
|
C | CAAAAAAA others(18): Show |
12 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0054others(9): Show | 12 | HG00738.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.601-9291_601-9290i others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | |||||
| chr22:17717380
|
C | CAAAAAAA others(19): Show |
9 | a0001c0001t0003g0024a0001c0001t0003g0027a0001c0001t0003g0029others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-9291_601-9290i others(28): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | |||||
| chr22:17717380
|
C | CAAAAAAA others(20): Show |
5 | a0001c0001t0003g0025a0001c0001t0003g0026a0001c0001t0003g0252others(2): Show | 5 | HG02647.hp2 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-9291_601-9290i others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | |||||
| chr22:17717380
|
C | CAAAAAAA others(26): Show |
1 | a0004c0006t0001g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.601-9291_601-9290i others(35): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | |||||
| chr22:17717380
|
C | CAAAAAAA others(27): Show |
1 | a0004c0006t0049g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.601-9291_601-9290i others(36): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | |||||
| chr22:17717380
|
C | CAAAAAAA others(28): Show |
1 | a0004c0006t0001g0092 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.601-9291_601-9290i others(37): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | |||||
| chr22:17717380
|
C | CAAAAAAA others(38): Show |
1 | a0004c0006t0063g0093 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.601-9291_601-9290i others(47): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | |||||
| chr22:17717439
|
C | T | 1 | a0001c0002t0012g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.601-9238C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717439 | ||||||
| chr22:17717459
|
T | G | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-9218T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717459 | ||||||
| chr22:17717464
|
T | G | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.601-9213T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717464 | ||||||
| chr22:17717500
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-9177G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717500 | ||||||
| chr22:17717586
|
C | T | 1 | a0001c0002t0006g0066 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.601-9091C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717586 | ||||||
| chr22:17717620
|
G | A | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.601-9057G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717620 | ||||||
| chr22:17717706
|
A | G | 2 | a0001c0001t0064g0304a0001c0001t0065g0103 | 2 | HG01255.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.601-8971A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717706 | ||||||
| chr22:17717737
|
T | C | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-8940T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717737 | ||||||
| chr22:17717914
|
C | T | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-8763C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717914 | ||||||
| chr22:17717947
|
C | T | 6 | a0001c0001t0003g0034a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | NA18955.hp1 NA18989.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-8730C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717947 | ||||||
| chr22:17717960
|
G | A | 1 | a0004c0006t0001g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.601-8717G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717960 | ||||||
| chr22:17718044
|
G | A | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.601-8633G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718044 | ||||||
| chr22:17718112
|
G | T | 15 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(12): Show | 15 | HG00099.hp2 HG00738.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.601-8565G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718112 | ||||||
| chr22:17718438
|
C | T | 72 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.601-8239C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718438 | ||||||
| chr22:17718529
|
C | T | 1 | a0001c0002t0027g0006 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.601-8148C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718529 | ||||||
| chr22:17718730
|
C | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-7947C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718730 | ||||||
| chr22:17718732
|
T | G | 22 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.601-7945T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718732 | ||||||
| chr22:17718760
|
G | C | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.601-7917G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718760 | ||||||
| chr22:17718835
|
G | C | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-7842G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718835 | ||||||
| chr22:17718839
|
C | G | 1 | a0001c0001t0062g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.601-7838C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718839 | ||||||
| chr22:17718875
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-7802G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718875 | ||||||
| chr22:17718875
|
G | T | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-7802G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718875 | ||||||
| chr22:17718947
|
T | C | 136 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(133): Show | 136 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.601-7730T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718947 | ||||||
| chr22:17718988
|
G | A | 1 | a0001c0001t0005g0242 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.601-7689G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718988 | ||||||
| chr22:17719003
|
C | T | 1 | a0006c0010t0001g0263 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601-7674C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719003 | ||||||
| chr22:17719021
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.601-7656G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719021 | ||||||
| chr22:17719153
|
C | CA | 52 | a0001c0001t0002g0169a0001c0001t0002g0172a0001c0001t0002g0210others(49): Show | 52 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.601-7500dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719153 | |||||
| chr22:17719153
|
C | CAA | 38 | a0001c0001t0003g0027a0001c0001t0003g0046a0001c0001t0003g0051others(35): Show | 38 | HG00099.hp2 HG00423.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.601-7501_601-7500d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719153 | |||||
| chr22:17719153
|
C | CAAA | 9 | a0001c0002t0006g0066a0001c0002t0006g0069a0001c0002t0006g0071others(6): Show | 9 | HG00738.hp1 HG01361.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.601-7502_601-7500d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719153 | |||||
| chr22:17719153
|
CA | C | 14 | a0001c0001t0002g0209a0001c0001t0005g0117a0001c0001t0007g0096others(11): Show | 14 | HG01081.hp2 HG01169.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.601-7500delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719153 | |||||
| chr22:17719206
|
A | C | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-7471A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719206 | ||||||
| chr22:17719266
|
A | G | 2 | a0001c0009t0004g0157a0001c0009t0004g0158 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.601-7411A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719266 | ||||||
| chr22:17719273
|
A | C | 1 | a0001c0001t0002g0194 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.601-7404A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719273 | ||||||
| chr22:17719363
|
A | G | 257 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.601-7314A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719363 | ||||||
| chr22:17719370
|
G | A | 1 | a0006c0010t0001g0263 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601-7307G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719370 | ||||||
| chr22:17719384
|
C | T | 21 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.601-7293C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719384 | ||||||
| chr22:17719441
|
A | G | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.601-7236A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719441 | ||||||
| chr22:17719541
|
G | A | 2 | a0001c0001t0005g0059a0001c0001t0005g0060 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.601-7136G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719541 | ||||||
| chr22:17719549
|
C | G | 4 | a0001c0001t0004g0098a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02738.hp1 HG03834.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-7128C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719549 | ||||||
| chr22:17719701
|
C | T | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-6976C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719701 | ||||||
| chr22:17719764
|
G | C | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.601-6913G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719764 | ||||||
| chr22:17719827
|
C | CAA | 20 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0226others(17): Show | 20 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.601-6828_601-6827d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719827 | |||||
| chr22:17719827
|
CAAAAAAA others(3): Show |
C | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.601-6836_601-6827d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719827 | |||||
| chr22:17719827
|
CAAAAAAA others(4): Show |
C | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.601-6837_601-6827d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719827 | |||||
| chr22:17719827
|
CAAAAAAA others(8): Show |
C | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-6841_601-6827d others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719827 | |||||
| chr22:17719846
|
A | AAAC | 60 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0116others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.601-6829_601-6828i others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719846 | |||||
| chr22:17719846
|
A | AAC | 70 | a0001c0001t0002g0128a0001c0001t0002g0209a0001c0001t0002g0216others(67): Show | 70 | HG00408.hp1 HG00423.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.601-6830_601-6829i others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719846 | |||||
| chr22:17719846
|
A | C | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0048g0140others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-6831A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719846 | ||||||
| chr22:17719868
|
A | ATGC | 13 | a0001c0001t0007g0008a0001c0001t0007g0009a0001c0001t0007g0012others(10): Show | 13 | HG01192.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-6807_601-6805d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719868 | |||||
| chr22:17719882
|
G | A | 1 | a0001c0002t0027g0006 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.601-6795G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719882 | ||||||
| chr22:17719897
|
A | G | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.601-6780A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719897 | ||||||
| chr22:17720084
|
A | G | 94 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-6593A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720084 | ||||||
| chr22:17720090
|
G | A | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-6587G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720090 | ||||||
| chr22:17720135
|
C | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-6542C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720135 | ||||||
| chr22:17720154
|
T | TTTCTTTC others(8): Show |
1 | a0001c0001t0060g0178 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.601-6521_601-6520i others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTCTTTC others(20): Show |
1 | a0001c0001t0011g0151 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.601-6521_601-6520i others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTCTTTC others(32): Show |
1 | a0001c0001t0010g0238 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.601-6521_601-6520i others(41): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTTC | 8 | a0001c0001t0003g0034a0001c0001t0003g0041a0001c0001t0003g0042others(5): Show | 8 | HG02965.hp1 NA18955.hp1 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-6498_601-6495d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTTCTTT others(5): Show |
6 | a0001c0001t0002g0176a0001c0001t0002g0195a0001c0001t0050g0250others(3): Show | 6 | HG01069.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-6506_601-6495d others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTTCTTT others(9): Show |
58 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(55): Show | 58 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.601-6510_601-6495d others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTTCTTT others(13): Show |
35 | a0001c0001t0002g0134a0001c0001t0002g0162a0001c0001t0002g0169others(32): Show | 35 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.601-6514_601-6495d others(22): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTTCTTT others(17): Show |
25 | a0001c0001t0002g0128a0001c0001t0002g0138a0001c0001t0002g0144others(22): Show | 25 | HG00323.hp1 HG00408.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.601-6518_601-6495d others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTTCTTT others(21): Show |
14 | a0001c0001t0002g0116a0001c0001t0002g0172a0001c0001t0002g0188others(11): Show | 14 | HG00280.hp1 HG01261.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.601-6522_601-6495d others(30): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTTCTTT others(25): Show |
10 | a0001c0001t0002g0211a0001c0001t0008g0227a0001c0001t0028g0303others(7): Show | 10 | HG00738.hp1 HG01934.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.601-6495_601-6494i others(34): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTTCTTT others(29): Show |
3 | a0001c0001t0008g0229a0001c0002t0006g0067a0001c0002t0012g0305 | 3 | HG02055.hp2 HG03041.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.601-6495_601-6494i others(38): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTTCTTT others(33): Show |
12 | a0001c0001t0008g0222a0001c0001t0008g0226a0001c0001t0008g0232others(9): Show | 12 | HG01169.hp2 HG01261.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.601-6495_601-6494i others(42): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTTCTTT others(37): Show |
12 | a0001c0001t0010g0146a0001c0001t0022g0237a0001c0001t0024g0243others(9): Show | 12 | HG00099.hp2 HG01167.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.601-6495_601-6494i others(46): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTTCTTT others(41): Show |
6 | a0001c0001t0008g0230a0001c0001t0020g0233a0001c0001t0036g0094others(3): Show | 6 | HG02257.hp1 HG02717.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-6495_601-6494i others(50): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTTCTTT others(45): Show |
4 | a0001c0001t0008g0223a0001c0001t0010g0235a0001c0002t0014g0064others(1): Show | 4 | HG02965.hp2 NA18953.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-6495_601-6494i others(54): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720154
|
T | TTTTCTTT others(53): Show |
1 | a0001c0001t0010g0219 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.601-6495_601-6494i others(62): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | |||||
| chr22:17720349
|
T | A | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.601-6328T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720349 | ||||||
| chr22:17720411
|
C | T | 2 | a0001c0001t0028g0302a0001c0001t0028g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.601-6266C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720411 | ||||||
| chr22:17720413
|
C | G | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.601-6264C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720413 | ||||||
| chr22:17720556
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-6121G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720556 | ||||||
| chr22:17720584
|
C | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-6093C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720584 | ||||||
| chr22:17720668
|
A | AT | 8 | a0001c0001t0002g0100a0001c0001t0004g0202a0001c0001t0008g0223others(5): Show | 8 | HG01192.hp1 HG04184.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-5993dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720668 | |||||
| chr22:17720690
|
C | T | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601-5987C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720690 | ||||||
| chr22:17720692
|
G | A | 1 | a0001c0001t0004g0208 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.601-5985G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720692 | ||||||
| chr22:17720766
|
T | C | 8 | a0001c0001t0003g0034a0001c0001t0003g0039a0001c0001t0003g0041others(5): Show | 8 | NA18955.hp1 NA18965.hp2 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-5911T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720766 | ||||||
| chr22:17720904
|
C | T | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.601-5773C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720904 | ||||||
| chr22:17720958
|
A | G | 6 | a0001c0002t0006g0066a0001c0002t0006g0067a0001c0002t0006g0079others(3): Show | 6 | HG00099.hp2 HG00738.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-5719A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720958 | ||||||
| chr22:17720992
|
C | T | 7 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-5685C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720992 | ||||||
| chr22:17721035
|
C | T | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601-5642C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721035 | ||||||
| chr22:17721095
|
G | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-5582G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721095 | ||||||
| chr22:17721104
|
A | G | 45 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(42): Show | 45 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.601-5573A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721104 | ||||||
| chr22:17721125
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-5552G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721125 | ||||||
| chr22:17721169
|
CA | C | 160 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.601-5496delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17721169 | |||||
| chr22:17721176
|
A | T | 22 | a0001c0001t0003g0037a0001c0001t0006g0070a0001c0002t0006g0066others(19): Show | 22 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.601-5501A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721176 | ||||||
| chr22:17721178
|
A | T | 95 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.601-5499A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721178 | ||||||
| chr22:17721180
|
A | AT | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-5497_601-5496i others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721180 | ||||||
| chr22:17721180
|
A | T | 113 | a0001c0001t0002g0141a0001c0001t0002g0212a0001c0001t0003g0002others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.601-5497A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721180 | ||||||
| chr22:17721182
|
T | A | 16 | a0001c0002t0026g0299a0001c0002t0026g0300a0001c0002t0035g0301others(13): Show | 16 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.601-5495T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721182 | ||||||
| chr22:17721184
|
T | A | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-5493T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721184 | ||||||
| chr22:17721208
|
G | A | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.601-5469G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721208 | ||||||
| chr22:17721285
|
G | A | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-5392G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721285 | ||||||
| chr22:17721325
|
A | G | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-5352A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721325 | ||||||
| chr22:17721381
|
A | G | 1 | a0001c0001t0004g0131 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.601-5296A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721381 | ||||||
| chr22:17721452
|
C | G | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.601-5225C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721452 | ||||||
| chr22:17721492
|
G | GT | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-5174dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17721492 | |||||
| chr22:17721525
|
A | ATTT | 202 | a0001c0001t0002g0099a0001c0001t0002g0111a0001c0001t0002g0112others(199): Show | 202 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.601-5136_601-5134d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17721525 | |||||
| chr22:17721525
|
A | ATTTT | 45 | a0001c0001t0002g0100a0001c0001t0002g0147a0001c0001t0002g0150others(42): Show | 45 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.601-5137_601-5134d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17721525 | |||||
| chr22:17721550
|
T | G | 94 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-5127T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721550 | ||||||
| chr22:17721650
|
A | G | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.601-5027A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721650 | ||||||
| chr22:17721707
|
G | A | 2 | a0001c0001t0022g0237a0001c0001t0022g0239 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.601-4970G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721707 | ||||||
| chr22:17721756
|
C | G | 15 | a0001c0001t0024g0243a0001c0001t0024g0244a0003c0004t0015g0080others(12): Show | 15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-4921C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721756 | ||||||
| chr22:17721821
|
C | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.601-4856C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721821 | ||||||
| chr22:17721853
|
G | A | 1 | a0001c0001t0008g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.601-4824G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721853 | ||||||
| chr22:17721860
|
C | T | 1 | a0001c0001t0004g0130 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.601-4817C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721860 | ||||||
| chr22:17721879
|
C | G | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.601-4798C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721879 | ||||||
| chr22:17721882
|
G | A | 1 | a0001c0002t0027g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.601-4795G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721882 | ||||||
| chr22:17721908
|
G | C | 94 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-4769G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721908 | ||||||
| chr22:17722061
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.601-4616A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722061 | ||||||
| chr22:17722076
|
T | C | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-4601T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722076 | ||||||
| chr22:17722090
|
AATAAGTA others(7): Show |
A | 1 | a0001c0001t0005g0142 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.601-4583_601-4570d others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722090 | |||||
| chr22:17722109
|
A | G | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-4568A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722109 | ||||||
| chr22:17722122
|
A | G | 1 | a0003c0004t0030g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.601-4555A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722122 | ||||||
| chr22:17722158
|
T | C | 1 | a0001c0001t0004g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.601-4519T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722158 | ||||||
| chr22:17722289
|
C | T | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601-4388C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722289 | ||||||
| chr22:17722314
|
A | G | 1 | a0001c0002t0012g0004 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601-4363A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722314 | ||||||
| chr22:17722375
|
AGG | A | 30 | a0001c0001t0002g0141a0001c0001t0003g0024a0001c0001t0003g0029others(27): Show | 30 | HG00099.hp2 HG00738.hp1 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.601-4299_601-4298d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722375 | |||||
| chr22:17722376
|
G | GGT | 16 | a0001c0001t0002g0100a0001c0001t0002g0150a0001c0001t0002g0156others(13): Show | 16 | HG02004.hp1 HG02300.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.601-4300_601-4299i others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | |||||
| chr22:17722376
|
G | GGTGC | 29 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0034others(26): Show | 29 | HG00140.hp2 HG01168.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.601-4300_601-4299i others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | |||||
| chr22:17722376
|
G | GGTGCGT | 10 | a0001c0001t0003g0107a0001c0001t0004g0163a0001c0001t0004g0177others(7): Show | 10 | HG00733.hp1 HG01243.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-4300_601-4299i others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | |||||
| chr22:17722376
|
G | GGTGCGTG others(3): Show |
9 | a0003c0004t0015g0080a0003c0004t0015g0253a0003c0004t0030g0101others(6): Show | 9 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-4300_601-4299i others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | |||||
| chr22:17722376
|
G | GGTGCGTG others(5): Show |
5 | a0003c0004t0015g0081a0003c0004t0016g0088a0004c0006t0001g0092others(2): Show | 5 | HG02280.hp2 HG02300.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-4300_601-4299i others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | |||||
| chr22:17722376
|
G | GGTGCGTG others(7): Show |
2 | a0003c0004t0016g0089a0004c0006t0001g0090 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.601-4300_601-4299i others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | |||||
| chr22:17722376
|
G | GGTGCGTG others(9): Show |
1 | a0003c0004t0016g0087 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.601-4300_601-4299i others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | |||||
| chr22:17722376
|
GGGGT | G | 13 | a0001c0001t0005g0185a0001c0001t0005g0241a0001c0001t0007g0009others(10): Show | 13 | HG00408.hp1 HG01192.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.601-4299_601-4296d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | |||||
| chr22:17722376
|
GGGGTGT | G | 32 | a0001c0001t0005g0007a0001c0001t0007g0008a0001c0001t0007g0012others(29): Show | 32 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.601-4299_601-4294d others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | |||||
| chr22:17722376
|
GGGGTGTG others(1): Show |
G | 7 | a0001c0001t0005g0242a0001c0001t0065g0103a0001c0002t0012g0003others(4): Show | 7 | HG00738.hp2 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-4299_601-4292d others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | |||||
| chr22:17722376
|
GGGGTGTG others(9): Show |
G | 1 | a0001c0001t0003g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601-4299_601-4284d others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | |||||
| chr22:17722378
|
G | C | 16 | a0001c0001t0002g0100a0001c0001t0002g0150a0001c0001t0002g0156others(13): Show | 16 | HG02004.hp1 HG02300.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.601-4299G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722378 | ||||||
| chr22:17722378
|
G | GGT | 3 | a0001c0002t0001g0247a0002c0003t0001g0270a0002c0003t0001g0292 | 3 | HG01258.hp2 HG02698.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.601-4258_601-4257d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722378 | |||||
| chr22:17722378
|
G | T | 159 | a0001c0001t0002g0099a0001c0001t0002g0111a0001c0001t0002g0112others(156): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.601-4299G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722378 | ||||||
| chr22:17722380
|
T | C | 100 | a0001c0001t0002g0099a0001c0001t0002g0111a0001c0001t0002g0112others(97): Show | 100 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.601-4297T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722380 | ||||||
| chr22:17722382
|
T | C | 30 | a0001c0001t0002g0141a0001c0001t0003g0024a0001c0001t0003g0029others(27): Show | 30 | HG00099.hp2 HG00738.hp1 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.601-4295T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722382 | ||||||
| chr22:17722384
|
T | C | 13 | a0001c0001t0005g0185a0001c0001t0005g0241a0001c0001t0007g0009others(10): Show | 13 | HG00408.hp1 HG01192.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.601-4293T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722384 | ||||||
| chr22:17722386
|
T | C | 29 | a0001c0001t0005g0007a0001c0001t0007g0008a0001c0001t0007g0012others(26): Show | 29 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.601-4291T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722386 | ||||||
| chr22:17722388
|
T | C | 7 | a0001c0001t0005g0242a0001c0001t0065g0103a0001c0002t0012g0003others(4): Show | 7 | HG00738.hp2 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-4289T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722388 | ||||||
| chr22:17722396
|
T | C | 1 | a0001c0001t0003g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601-4281T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722396 | ||||||
| chr22:17722417
|
G | A | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-4260G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722417 | ||||||
| chr22:17722421
|
A | G | 26 | a0001c0001t0006g0070a0001c0002t0006g0066a0001c0002t0006g0067others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.601-4256A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722421 | ||||||
| chr22:17722664
|
A | T | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.601-4013A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722664 | ||||||
| chr22:17722791
|
C | T | 94 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-3886C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722791 | ||||||
| chr22:17722911
|
G | C | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-3766G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722911 | ||||||
| chr22:17723154
|
C | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0245 | 2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.601-3523C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723154 | ||||||
| chr22:17723173
|
C | T | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-3504C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723173 | ||||||
| chr22:17723181
|
CCT | C | 3 | a0001c0002t0026g0299a0001c0002t0026g0300a0001c0002t0035g0301 | 3 | HG02258.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.601-3489_601-3488d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17723181 | |||||
| chr22:17723232
|
G | T | 1 | a0001c0002t0052g0285 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.601-3445G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723232 | ||||||
| chr22:17723560
|
A | G | 1 | a0001c0001t0002g0134 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.601-3117A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723560 | ||||||
| chr22:17723570
|
T | C | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601-3107T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723570 | ||||||
| chr22:17723639
|
A | G | 7 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-3038A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723639 | ||||||
| chr22:17723656
|
C | T | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-3021C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723656 | ||||||
| chr22:17723701
|
G | A | 1 | a0001c0001t0062g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.601-2976G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723701 | ||||||
| chr22:17723734
|
A | C | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-2943A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723734 | ||||||
| chr22:17723750
|
T | C | 1 | a0001c0001t0003g0024 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.601-2927T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723750 | ||||||
| chr22:17723762
|
G | A | 2 | a0005c0008t0019g0255a0005c0008t0019g0256 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.601-2915G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723762 | ||||||
| chr22:17723772
|
A | G | 13 | a0003c0004t0015g0080a0003c0004t0015g0081a0003c0004t0015g0253others(10): Show | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-2905A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723772 | ||||||
| chr22:17723777
|
A | G | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-2900A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723777 | ||||||
| chr22:17723887
|
T | C | 257 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.601-2790T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723887 | ||||||
| chr22:17723888
|
G | A | 1 | a0001c0001t0002g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.601-2789G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723888 | ||||||
| chr22:17723931
|
C | CA | 25 | a0001c0001t0004g0132a0001c0001t0004g0201a0001c0001t0006g0070others(22): Show | 25 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.601-2736dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17723931 | |||||
| chr22:17723931
|
C | CAA | 12 | a0003c0004t0015g0080a0003c0004t0015g0253a0003c0004t0016g0087others(9): Show | 12 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.601-2737_601-2736d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17723931 | |||||
| chr22:17723983
|
G | C | 2 | a0001c0002t0001g0286a0001c0002t0001g0297 | 2 | HG00741.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.601-2694G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723983 | ||||||
| chr22:17724003
|
T | A | 2 | a0001c0001t0024g0243a0001c0001t0024g0244 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-2674T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724003 | ||||||
| chr22:17724025
|
C | T | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-2652C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724025 | ||||||
| chr22:17724259
|
C | T | 1 | a0001c0001t0005g0241 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.601-2418C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724259 | ||||||
| chr22:17724372
|
C | T | 1 | a0001c0001t0066g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.601-2305C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724372 | ||||||
| chr22:17724447
|
T | A | 1 | a0008c0011t0023g0106 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.601-2230T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724447 | ||||||
| chr22:17724454
|
C | T | 15 | a0001c0001t0008g0223a0001c0001t0008g0227a0001c0001t0008g0230others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-2223C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724454 | ||||||
| chr22:17724485
|
T | C | 80 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.601-2192T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724485 | ||||||
| chr22:17724750
|
T | C | 1 | a0001c0001t0003g0030 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.601-1927T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724750 | ||||||
| chr22:17724961
|
C | A | 1 | a0001c0002t0001g0281 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.601-1716C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724961 | ||||||
| chr22:17724964
|
G | C | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-1713G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724964 | ||||||
| chr22:17725014
|
C | CA | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-1662dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17725014 | |||||
| chr22:17725045
|
G | A | 1 | a0001c0001t0003g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601-1632G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725045 | ||||||
| chr22:17725161
|
T | G | 257 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.601-1516T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725161 | ||||||
| chr22:17725278
|
G | A | 1 | a0001c0001t0005g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.601-1399G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725278 | ||||||
| chr22:17725300
|
A | C | 1 | a0001c0002t0052g0285 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.601-1377A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725300 | ||||||
| chr22:17725649
|
C | T | 6 | a0001c0001t0017g0013a0001c0001t0017g0019a0001c0001t0017g0020others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-1028C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725649 | ||||||
| chr22:17725762
|
AT | A | 6 | a0001c0001t0002g0099a0001c0001t0003g0051a0001c0001t0005g0242others(3): Show | 6 | HG00738.hp2 HG01255.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-902delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17725762 | |||||
| chr22:17725870
|
A | G | 1 | a0001c0001t0047g0135 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.601-807A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725870 | ||||||
| chr22:17725875
|
G | A | 112 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.601-802G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725875 | ||||||
| chr22:17725998
|
C | T | 254 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.601-679C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725998 | ||||||
| chr22:17726110
|
G | A | 46 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.601-567G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17726110 | ||||||
| chr22:17726212
|
G | A | 4 | a0004c0006t0001g0090a0004c0006t0001g0092a0004c0006t0049g0091others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-465G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17726212 | ||||||
| chr22:17726350
|
TA | T | 157 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0111others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.601-308delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17726350 | |||||
| chr22:17726350
|
TAA | T | 92 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(89): Show | 92 | HG00140.hp2 HG00733.hp1 HG01167.hp1 others(89): Show |
intron_variant | MODIFIER | c.601-309_601-308del others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17726350 | |||||
| chr22:17726351
|
A | T | 1 | a0006c0010t0001g0263 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601-326A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17726351 | ||||||
| chr22:17726363
|
A | C | 3 | a0005c0008t0019g0255a0005c0008t0019g0256a0005c0008t0019g0298 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601-314A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17726363 | ||||||
| chr22:17726545
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0004a0001c0002t0012g0305others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-132G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17726545 |