Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 317 |
|---|---|
| ensemblid | ENSG00000120868.14 |
| hgncid | 576 |
| symbol | APAF1 |
| name | apoptotic peptidase activating factor 1 |
| refseq_nuc | NM_181861.2 |
| refseq_prot | NP_863651.1 |
| ensembl_nuc | ENST00000551964.6 |
| ensembl_prot | ENSP00000448165.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 98645290 |
| end | 98735433 |
| strand | + |
| ver | v1.2 |
| region | chr12:98645290-98735433 |
| region5000 | chr12:98640290-98740433 |
| regionname0 | APAF1_chr12_98645290_98735433 |
| regionname5000 | APAF1_chr12_98640290_98740433 |
| 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 | 1248 | 355 | 84 | 57 | 153 | 12 | 47 | 119 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0002 | 0/0 | 1248 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0003 | 0/0 | 1248 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0004 | 0/0 | 1248 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0005 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0006 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0007 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0008 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0009 | 0/0 | 1248 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| 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 | 1/1 | 3747 | 348 | 79 | 57 | 151 | 12 | 47 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| c0002 | 0/0 | 3747 | 3 | 3 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| c0003 | 0/0 | 3747 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| c0004 | 0/0 | 3747 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| c0005 | 0/0 | 3747 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| c0006 | 0/0 | 3747 | 2 | 0 | 0 | 2 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| c0007 | 0/0 | 3747 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| c0008 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| c0009 | 0/0 | 3747 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| c0010 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| c0011 | 0/0 | 3747 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| c0012 | 0/0 | 3747 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| c0013 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| 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 | 3455 | 165 | 30 | 32 | 65 | 7 | 30 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0002 | 0/0 | 3454 | 35 | 1 | 3 | 26 | 0 | 5 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0003 | 0/0 | 3454 | 30 | 2 | 0 | 25 | 0 | 3 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0004 | 0/1 | 3454 | 27 | 12 | 7 | 0 | 3 | 4 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0005 | 0/0 | 3455 | 21 | 0 | 0 | 21 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0006 | 0/0 | 3454 | 16 | 0 | 6 | 8 | 1 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0007 | 0/0 | 3454 | 8 | 6 | 0 | 0 | 0 | 2 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0008 | 0/0 | 3454 | 7 | 6 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0009 | 0/0 | 3455 | 5 | 5 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0010 | 0/0 | 3455 | 5 | 0 | 0 | 5 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0011 | 0/0 | 3454 | 4 | 0 | 0 | 4 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0012 | 0/0 | 3454 | 4 | 4 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0013 | 0/0 | 3454 | 3 | 3 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0014 | 0/0 | 3455 | 3 | 2 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0015 | 0/0 | 3454 | 3 | 3 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0016 | 0/0 | 3455 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0017 | 0/0 | 3454 | 2 | 0 | 2 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0018 | 0/0 | 3455 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0019 | 0/0 | 3455 | 2 | 0 | 0 | 0 | 1 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0020 | 0/0 | 3455 | 2 | 0 | 2 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0021 | 0/0 | 3455 | 2 | 0 | 0 | 1 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0022 | 0/0 | 3454 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0023 | 0/0 | 3455 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0024 | 0/0 | 3454 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0025 | 0/0 | 3454 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0026 | 0/0 | 3454 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0027 | 0/0 | 3454 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0028 | 0/0 | 3455 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0029 | 0/0 | 3454 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0030 | 0/0 | 3454 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0031 | 0/0 | 3455 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0032 | 0/0 | 3455 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0033 | 0/0 | 3454 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0034 | 0/0 | 3454 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0035 | 0/0 | 3454 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0036 | 0/0 | 3454 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0037 | 0/0 | 3454 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0038 | 0/0 | 3454 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| t0039 | 0/0 | 3454 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| 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 | 1/1 | 3747 | 348 | 79 | 57 | 151 | 12 | 47 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0002 | 0/0 | 3747 | 3 | 3 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0004 | 0/0 | 3747 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0010 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0013 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0002c0003 | 0/0 | 3747 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0003c0005 | 0/0 | 3747 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0004c0006 | 0/0 | 3747 | 2 | 0 | 0 | 2 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0005c0008 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0006c0012 | 0/0 | 3747 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0007c0011 | 0/0 | 3747 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0008c0009 | 0/0 | 3747 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0009c0007 | 0/0 | 3747 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 7201 | 160 | 29 | 32 | 62 | 7 | 29 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0002 | 0/0 | 7200 | 35 | 1 | 3 | 26 | 0 | 5 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0003 | 0/0 | 7200 | 30 | 2 | 0 | 25 | 0 | 3 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0004 | 0/1 | 7200 | 27 | 12 | 7 | 0 | 3 | 4 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0005 | 0/0 | 7201 | 21 | 0 | 0 | 21 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0006 | 0/0 | 7200 | 15 | 0 | 6 | 7 | 1 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0007 | 0/0 | 7200 | 2 | 0 | 0 | 0 | 0 | 2 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0008 | 0/0 | 7200 | 7 | 6 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0009 | 0/0 | 7201 | 5 | 5 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0010 | 0/0 | 7201 | 5 | 0 | 0 | 5 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0011 | 0/0 | 7200 | 3 | 0 | 0 | 3 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0012 | 0/0 | 7200 | 3 | 3 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0013 | 0/0 | 7200 | 3 | 3 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0014 | 0/0 | 7201 | 3 | 2 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0015 | 0/0 | 7200 | 3 | 3 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0016 | 0/0 | 7201 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0017 | 0/0 | 7200 | 2 | 0 | 2 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0018 | 0/0 | 7201 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0019 | 0/0 | 7201 | 2 | 0 | 0 | 0 | 1 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0020 | 0/0 | 7201 | 2 | 0 | 2 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0021 | 0/0 | 7201 | 2 | 0 | 0 | 1 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0022 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0024 | 0/0 | 7200 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0026 | 0/0 | 7200 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0027 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0028 | 0/0 | 7201 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0030 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0031 | 0/0 | 7201 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0033 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0034 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0035 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0036 | 0/0 | 7200 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0037 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0038 | 0/0 | 7200 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0001t0039 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0002t0001 | 0/0 | 7201 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0002t0023 | 0/0 | 7201 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0002t0032 | 0/0 | 7201 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0004t0007 | 0/0 | 7200 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0010t0001 | 0/0 | 7201 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0001c0013t0006 | 0/0 | 7200 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0002c0003t0007 | 0/0 | 7200 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0003c0005t0007 | 0/0 | 7200 | 2 | 2 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0004c0006t0001 | 0/0 | 7201 | 2 | 0 | 0 | 2 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0005c0008t0011 | 0/0 | 7200 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0006c0012t0001 | 0/0 | 7201 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0007c0011t0025 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0008c0009t0012 | 0/0 | 7200 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| a0009c0007t0029 | 0/0 | 7200 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | copy fasta | chr12 | 98640290 | 98740433 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0006g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0007g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0008g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0008g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0008g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0008g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0008g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0008g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0009g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0010g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0010g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0010g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0010g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0010g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0011g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0011g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0011g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0012g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0012g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0012g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0013g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0013g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0013g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0014g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0014g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0014g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0015g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0015g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0015g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0016g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0016g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0017g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0017g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0018g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0018g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0019g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0019g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0020g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0020g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0021g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0021g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0022g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0024g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0026g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0027g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0028g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0030g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0031g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0033g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0034g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0035g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0036g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0037g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0038g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0001t0039g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0002t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0002t0023g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0002t0032g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0004t0007g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0004t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0010t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0001c0013t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0002c0003t0007g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0002c0003t0007g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0003c0005t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0003c0005t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0004c0006t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0004c0006t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0005c0008t0011g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0006c0012t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0007c0011t0025g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0008c0009t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| a0009c0007t0029g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0288 | EUR | GBR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00140 | hp2 | a0001 | c0001 | t0019 | g0215 | EUR | GBR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0191 | EUR | FIN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0322 | EUR | FIN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0349 | EAS | CHS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0126 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0312 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0190 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0363 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01081 | hp1 | a0001 | c0001 | t0036 | g0300 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01099 | hp1 | a0001 | c0001 | t0020 | g0351 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01109 | hp1 | a0009 | c0007 | t0029 | g0304 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01109 | hp2 | a0001 | c0001 | t0020 | g0352 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0178 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0179 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01192 | hp2 | a0001 | c0001 | t0026 | g0151 | AMR | PUR | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0171 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01257 | hp2 | a0001 | c0001 | t0017 | g0203 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01258 | hp1 | a0001 | c0001 | t0017 | g0202 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0180 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0165 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01433 | hp1 | a0001 | c0001 | t0038 | g0320 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0362 | EUR | IBS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0197 | EUR | IBS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0196 | EUR | IBS | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0302 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0042 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01891 | hp2 | a0001 | c0001 | t0030 | g0007 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0160 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02004 | hp2 | a0001 | c0001 | t0031 | g0252 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02129 | hp2 | a0001 | c0001 | t0024 | g0162 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0082 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0166 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CDX | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | CDX | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0311 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02257 | hp2 | a0001 | c0001 | t0027 | g0214 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02258 | hp2 | a0001 | c0004 | t0007 | g0226 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02273 | hp1 | a0001 | c0001 | t0006 | g0163 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02280 | hp2 | a0002 | c0003 | t0007 | g0353 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02293 | hp1 | a0001 | c0001 | t0006 | g0222 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0127 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0095 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | KHV | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02572 | hp1 | a0003 | c0005 | t0007 | g0220 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02622 | hp1 | a0001 | c0001 | t0016 | g0045 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0313 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0188 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0212 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0124 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02717 | hp1 | a0008 | c0009 | t0012 | g0211 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02717 | hp2 | a0007 | c0011 | t0025 | g0204 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0177 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02735 | hp1 | a0001 | c0001 | t0021 | g0321 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0205 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02818 | hp1 | a0003 | c0005 | t0007 | g0219 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02886 | hp1 | a0001 | c0001 | t0033 | g0213 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02895 | hp1 | a0001 | c0001 | t0037 | g0299 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0122 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0306 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0305 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02897 | hp2 | a0001 | c0001 | t0014 | g0123 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0308 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0084 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0355 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02970 | hp2 | a0001 | c0002 | t0032 | g0217 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0199 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0070 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03130 | hp2 | a0001 | c0001 | t0022 | g0307 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03139 | hp1 | a0002 | c0003 | t0007 | g0354 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03195 | hp1 | a0001 | c0001 | t0034 | g0208 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0338 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03453 | hp2 | a0001 | c0001 | t0028 | g0005 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0310 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03490 | hp2 | a0001 | c0001 | t0007 | g0250 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0145 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03516 | hp1 | a0001 | c0002 | t0023 | g0309 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03516 | hp2 | a0001 | c0001 | t0012 | g0210 | AFR | ESN | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03579 | hp2 | a0001 | c0004 | t0007 | g0225 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0359 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0361 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0189 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0315 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0065 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0198 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03942 | hp2 | a0001 | c0001 | t0019 | g0216 | SAS | BEB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0342 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04204 | hp1 | a0006 | c0012 | t0001 | g0360 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04228 | hp1 | a0001 | c0001 | t0014 | g0293 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0323 | SAS | STU | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18522 | hp1 | a0001 | c0001 | t0015 | g0129 | AFR | YRI | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | YRI | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | CHB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0255 | AFR | YRI | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18940 | hp2 | a0001 | c0001 | t0010 | g0292 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18946 | hp1 | a0001 | c0001 | t0006 | g0157 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18946 | hp2 | a0004 | c0006 | t0001 | g0356 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18949 | hp2 | a0001 | c0001 | t0021 | g0350 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18950 | hp2 | a0001 | c0001 | t0011 | g0135 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18952 | hp2 | a0001 | c0001 | t0010 | g0296 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0076 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18966 | hp2 | a0001 | c0010 | t0001 | g0029 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0115 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18975 | hp2 | a0001 | c0001 | t0011 | g0140 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18979 | hp1 | a0001 | c0001 | t0006 | g0164 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18982 | hp2 | a0001 | c0001 | t0010 | g0295 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18984 | hp2 | a0001 | c0001 | t0010 | g0291 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18989 | hp1 | a0001 | c0001 | t0006 | g0174 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18993 | hp1 | a0001 | c0013 | t0006 | g0153 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0087 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19005 | hp2 | a0001 | c0001 | t0006 | g0169 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19012 | hp2 | a0001 | c0001 | t0010 | g0297 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19030 | hp1 | a0001 | c0001 | t0018 | g0009 | AFR | LWK | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0079 | AFR | LWK | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0318 | AFR | LWK | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19043 | hp2 | a0001 | c0001 | t0039 | g0008 | AFR | LWK | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19054 | hp2 | a0004 | c0006 | t0001 | g0256 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19056 | hp1 | a0001 | c0001 | t0006 | g0223 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0086 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19065 | hp1 | a0005 | c0008 | t0011 | g0142 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19072 | hp2 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19078 | hp1 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19083 | hp2 | a0001 | c0001 | t0011 | g0132 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19240 | hp1 | a0001 | c0001 | t0015 | g0128 | AFR | YRI | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA19240 | hp2 | a0001 | c0001 | t0013 | g0301 | AFR | YRI | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0218 | AFR | ASW | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ASW | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0200 | SAS | GIH | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG02486 | hp2 | a0001 | c0001 | t0013 | g0303 | AFR | ACB | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03471 | hp1 | a0001 | c0001 | t0016 | g0071 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| HG03471 | hp2 | a0001 | c0001 | t0035 | g0201 | AFR | MSL | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | USA | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | USA | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA21309 | hp1 | a0001 | c0001 | t0018 | g0010 | AFR | LWK | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0192 | REF | REF | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0241 | REF | REF | APAF1_chr12_98640290_98740433 | APAF1 | chr12 | 98640290 | 98740433 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:98648493
|
A | G | 1 | a0004 | 2 | NA18946.hp2 NA19054.hp2 |
missense_variant | MODERATE | c.134A>G | p.Asn45Ser | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 2/27 | 721/7201 | 134/3747 | 45/1248 | chr12 | 98648493 | ||
| chr12:98649657
|
G | A | 1 | a0009 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.499G>A | p.Ala167Thr | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/27 | 1086/7201 | 499/3747 | 167/1248 | chr12 | 98649657 | ||
| chr12:98662550
|
G | A | 1 | a0005 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.805G>A | p.Val269Ile | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 6/27 | 1392/7201 | 805/3747 | 269/1248 | chr12 | 98662550 | ||
| chr12:98666295
|
C | T | 1 | a0006 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.1300C>T | p.Arg434Cys | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/27 | 1887/7201 | 1300/3747 | 434/1248 | chr12 | 98666295 | ||
| chr12:98666331
|
A | T | 1 | a0002 | 2 | HG02280.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.1336A>T | p.Thr446Ser | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/27 | 1923/7201 | 1336/3747 | 446/1248 | chr12 | 98666331 | ||
| chr12:98667559
|
C | T | 1 | a0007 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1409C>T | p.Pro470Leu | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/27 | 1996/7201 | 1409/3747 | 470/1248 | chr12 | 98667559 | ||
| chr12:98683182
|
G | C | 1 | a0008 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.2086G>C | p.Asp696His | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/27 | 2673/7201 | 2086/3747 | 696/1248 | chr12 | 98683182 | ||
| chr12:98715542
|
C | A | 1 | a0003 | 2 | HG02572.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.3074C>A | p.Ala1025Asp | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/27 | 3661/7201 | 3074/3747 | 1025/1248 | chr12 | 98715542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:98665590
|
A | G | 1 | a0001c0013 | 1 | NA18993.hp1 | synonymous_variant | LOW | c.993A>G | p.Leu331Leu | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 8/27 | 1580/7201 | 993/3747 | 331/1248 | chr12 | 98665590 | ||
| chr12:98665674
|
T | C | 2 | a0001c0002a0002c0003 | 5 | HG02280.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
synonymous_variant | LOW | c.1077T>C | p.Tyr359Tyr | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 8/27 | 1664/7201 | 1077/3747 | 359/1248 | chr12 | 98665674 | ||
| chr12:98699518
|
G | A | 1 | a0001c0010 | 1 | NA18966.hp2 | synonymous_variant | LOW | c.2415G>A | p.Ser805Ser | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/27 | 3002/7201 | 2415/3747 | 805/1248 | chr12 | 98699518 | ||
| chr12:98699524
|
T | G | 1 | a0001c0004 | 2 | HG02258.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.2421T>G | p.Ser807Ser | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/27 | 3008/7201 | 2421/3747 | 807/1248 | chr12 | 98699524 | ||
| chr12:98712429
|
C | T | 1 | a0001c0004 | 2 | HG02258.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.2952C>T | p.Ala984Ala | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/27 | 3539/7201 | 2952/3747 | 984/1248 | chr12 | 98712429 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:98645389
|
G | A | 3 | a0001c0001t0008a0001c0001t0022a0001c0002t0023 | 9 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-488G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/27 | 2971 | chr12 | 98645389 | |||||
| chr12:98645393
|
A | G | 1 | a0001c0001t0015 | 3 | HG02451.hp1 NA18522.hp1 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-484A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/27 | 2967 | chr12 | 98645393 | |||||
| chr12:98645405
|
G | A | 8 | a0001c0001t0003a0001c0001t0006a0001c0001t0011others(5): Show | 53 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(50): Show |
5_prime_UTR_variant | MODIFIER | c.-472G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/27 | 2955 | chr12 | 98645405 | |||||
| chr12:98645475
|
C | T | 1 | a0001c0001t0039 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-402C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/27 | 2885 | chr12 | 98645475 | |||||
| chr12:98645477
|
G | A | 1 | a0001c0001t0016 | 2 | HG02622.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-400G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/27 | 2883 | chr12 | 98645477 | |||||
| chr12:98645548
|
C | G | 3 | a0001c0001t0002a0001c0001t0021a0001c0001t0038 | 38 | HG00408.hp1 HG00438.hp1 HG00621.hp2 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-329C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/27 | 2812 | chr12 | 98645548 | |||||
| chr12:98645567
|
G | C | 1 | a0001c0001t0027 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-310G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/27 | 2793 | chr12 | 98645567 | |||||
| chr12:98645592
|
C | G | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG01081.hp1 HG02895.hp1 |
5_prime_UTR_variant | MODIFIER | c.-285C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/27 | 2768 | chr12 | 98645592 | |||||
| chr12:98645636
|
C | T | 1 | a0001c0001t0038 | 1 | HG01433.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-241C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/27 | chr12 | 98645636 | ||||||
| chr12:98645689
|
G | T | 3 | a0001c0001t0002a0001c0001t0021a0001c0001t0038 | 38 | HG00408.hp1 HG00438.hp1 HG00621.hp2 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-188G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/27 | 2671 | chr12 | 98645689 | |||||
| chr12:98645695
|
G | A | 1 | a0001c0001t0028 | 1 | HG03453.hp2 | 5_prime_UTR_variant | MODIFIER | c.-182G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/27 | 2665 | chr12 | 98645695 | |||||
| chr12:98648349
|
T | G | 1 | a0009c0007t0029 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 2/27 | 11 | chr12 | 98648349 | |||||
| chr12:98732772
|
C | T | 1 | a0001c0001t0010 | 5 | NA18940.hp2 NA18952.hp2 NA18982.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*206C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 206 | chr12 | 98732772 | |||||
| chr12:98732870
|
A | G | 1 | a0001c0001t0035 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*304A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 304 | chr12 | 98732870 | |||||
| chr12:98732992
|
G | T | 7 | a0001c0001t0010a0001c0001t0012a0001c0001t0014others(4): Show | 15 | HG02257.hp2 HG02647.hp2 HG02717.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*426G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 426 | chr12 | 98732992 | |||||
| chr12:98733133
|
C | A | 1 | a0001c0001t0024 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*567C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 567 | chr12 | 98733133 | |||||
| chr12:98733222
|
C | A | 2 | a0001c0001t0013a0009c0007t0029 | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*656C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 656 | chr12 | 98733222 | |||||
| chr12:98733260
|
G | A | 1 | a0001c0001t0022 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*694G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 694 | chr12 | 98733260 | |||||
| chr12:98733323
|
G | A | 2 | a0001c0001t0009a0001c0001t0028 | 6 | HG01891.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*757G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 757 | chr12 | 98733323 | |||||
| chr12:98733539
|
C | A | 1 | a0007c0011t0025 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*973C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 973 | chr12 | 98733539 | |||||
| chr12:98733653
|
T | G | 12 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(9): Show | 72 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1087T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 1087 | chr12 | 98733653 | |||||
| chr12:98733738
|
C | T | 1 | a0001c0001t0034 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1172C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 1172 | chr12 | 98733738 | |||||
| chr12:98733917
|
GA | G | 35 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(32): Show | 165 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*1354delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 1354 | INFO_REALIGN_3_PRIME | chr12 | 98733917 | ||||
| chr12:98733968
|
C | T | 1 | a0001c0001t0033 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1402C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 1402 | chr12 | 98733968 | |||||
| chr12:98733981
|
T | C | 1 | a0001c0001t0019 | 2 | HG00140.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1415T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 1415 | chr12 | 98733981 | |||||
| chr12:98734223
|
A | T | 23 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(20): Show | 93 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1657A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 1657 | chr12 | 98734223 | |||||
| chr12:98734224
|
T | C | 23 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(20): Show | 93 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1658T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 1658 | chr12 | 98734224 | |||||
| chr12:98734324
|
T | C | 1 | a0001c0001t0036 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1758T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 1758 | chr12 | 98734324 | |||||
| chr12:98734464
|
T | C | 1 | a0001c0001t0018 | 2 | NA19030.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1898T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 1898 | chr12 | 98734464 | |||||
| chr12:98734514
|
A | T | 1 | a0001c0001t0017 | 2 | HG01257.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1948A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 1948 | chr12 | 98734514 | |||||
| chr12:98734579
|
G | A | 1 | a0001c0001t0031 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2013G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 2013 | chr12 | 98734579 | |||||
| chr12:98734943
|
C | T | 2 | a0001c0002t0023a0001c0002t0032 | 2 | HG02970.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2377C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 2377 | chr12 | 98734943 | |||||
| chr12:98735063
|
C | T | 1 | a0001c0001t0030 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2497C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 2497 | chr12 | 98735063 | |||||
| chr12:98735094
|
G | A | 1 | a0001c0001t0005 | 21 | HG02080.hp1 HG02135.hp1 HG02523.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2528G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 2528 | chr12 | 98735094 | |||||
| chr12:98735241
|
A | AT | 4 | a0001c0001t0010a0001c0001t0014a0001c0001t0019others(1): Show | 12 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2682dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 2683 | INFO_REALIGN_3_PRIME | chr12 | 98735241 | ||||
| chr12:98735280
|
T | C | 1 | a0001c0001t0026 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2714T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 2714 | chr12 | 98735280 | |||||
| chr12:98735282
|
A | C | 2 | a0001c0001t0011a0005c0008t0011 | 4 | NA18950.hp2 NA18975.hp2 NA19065.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2716A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 2716 | chr12 | 98735282 | |||||
| chr12:98735419
|
T | C | 2 | a0001c0001t0019a0001c0001t0020 | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2853T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 27/27 | 2853 | chr12 | 98735419 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:98646006
|
A | G | 6 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0361others(3): Show | 6 | HG01069.hp2 HG01515.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+171A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98646006 | ||||||
| chr12:98646070
|
A | G | 1 | a0001c0001t0001g0357 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-42+235A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98646070 | ||||||
| chr12:98646072
|
A | G | 1 | a0004c0006t0001g0356 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-42+237A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98646072 | ||||||
| chr12:98646339
|
C | T | 3 | a0001c0002t0001g0355a0002c0003t0007g0353a0002c0003t0007g0354 | 3 | HG02280.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-42+504C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98646339 | ||||||
| chr12:98646381
|
T | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0018g0009others(4): Show | 7 | HG01891.hp2 HG03098.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-42+546T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98646381 | ||||||
| chr12:98646705
|
T | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 4 | NA18612.hp2 NA18952.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42+870T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98646705 | ||||||
| chr12:98647027
|
AT | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(109): Show | 113 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.-42+1193delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98647027 | ||||||
| chr12:98647247
|
C | G | 2 | a0001c0001t0020g0351a0001c0001t0020g0352 | 2 | HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-41-1072C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98647247 | ||||||
| chr12:98647253
|
T | TA | 13 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(10): Show | 13 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.-41-1050dupA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 98647253 | |||||
| chr12:98647253
|
TA | T | 37 | a0001c0001t0002g0314a0001c0001t0002g0315a0001c0001t0002g0316others(34): Show | 37 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-41-1050delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 98647253 | |||||
| chr12:98647273
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0018g0009others(4): Show | 7 | HG01891.hp2 HG03098.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41-1046G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98647273 | ||||||
| chr12:98647379
|
G | GT | 10 | a0001c0001t0001g0120a0001c0001t0008g0305a0001c0001t0008g0306others(7): Show | 10 | HG00544.hp2 HG00735.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41-929dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 98647379 | |||||
| chr12:98647426
|
A | G | 6 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(3): Show | 6 | HG01081.hp1 HG01109.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-893A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98647426 | ||||||
| chr12:98647705
|
G | GT | 18 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0116others(15): Show | 18 | HG00621.hp2 HG01433.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-41-594dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 98647705 | |||||
| chr12:98647705
|
GT | G | 110 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0206others(107): Show | 110 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-41-594delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 98647705 | |||||
| chr12:98647930
|
A | G | 1 | a0001c0001t0001g0363 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-41-389A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98647930 | ||||||
| chr12:98647947
|
G | T | 1 | a0001c0001t0002g0323 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-41-372G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98647947 | ||||||
| chr12:98647949
|
TTGAGCTA others(7): Show |
T | 1 | a0001c0001t0002g0323 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-41-366_-41-353del others(14): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 98647949 | |||||
| chr12:98648127
|
G | C | 167 | a0001c0001t0001g0294a0001c0001t0002g0209a0001c0001t0002g0221others(164): Show | 167 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-41-192G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98648127 | ||||||
| chr12:98648227
|
T | A | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-41-92T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 1/26 | chr12 | 98648227 | ||||||
| chr12:98648519
|
C | T | 1 | a0001c0001t0036g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.138+22C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 2/26 | chr12 | 98648519 | ||||||
| chr12:98649099
|
A | G | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.328+284A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 3/26 | chr12 | 98649099 | ||||||
| chr12:98649271
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.329-216C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 3/26 | chr12 | 98649271 | ||||||
| chr12:98649375
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.329-112T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 3/26 | chr12 | 98649375 | ||||||
| chr12:98649429
|
A | G | 86 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(83): Show | 86 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.329-58A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 3/26 | chr12 | 98649429 | ||||||
| chr12:98649756
|
C | T | 1 | a0001c0001t0002g0348 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.526+72C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98649756 | ||||||
| chr12:98649875
|
TAGC | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0289a0001c0001t0001g0290 | 4 | HG00642.hp1 HG00733.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+194_526+196del others(3): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98649875 | |||||
| chr12:98649905
|
A | T | 167 | a0001c0001t0001g0294a0001c0001t0002g0209a0001c0001t0002g0221others(164): Show | 167 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.526+221A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98649905 | ||||||
| chr12:98649915
|
T | G | 1 | a0001c0001t0001g0227 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.526+231T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98649915 | ||||||
| chr12:98650058
|
G | T | 1 | a0001c0001t0004g0205 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.526+374G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650058 | ||||||
| chr12:98650157
|
C | T | 8 | a0001c0001t0002g0221a0001c0001t0002g0315a0001c0001t0002g0316others(5): Show | 8 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+473C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650157 | ||||||
| chr12:98650224
|
C | T | 1 | a0001c0001t0010g0297 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.526+540C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650224 | ||||||
| chr12:98650286
|
C | T | 1 | a0001c0002t0001g0355 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.526+602C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650286 | ||||||
| chr12:98650379
|
G | A | 86 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(83): Show | 86 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.526+695G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650379 | ||||||
| chr12:98650440
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.526+756C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650440 | ||||||
| chr12:98650496
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.526+812T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650496 | ||||||
| chr12:98650502
|
G | GT | 6 | a0001c0001t0001g0110a0001c0001t0001g0119a0001c0001t0001g0298others(3): Show | 6 | HG00741.hp2 HG01081.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+831dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98650502 | |||||
| chr12:98650502
|
G | T | 3 | a0001c0001t0001g0111a0001c0001t0001g0207a0001c0001t0001g0287 | 3 | HG02055.hp1 HG02451.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.526+818G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650502 | ||||||
| chr12:98650510
|
T | G | 1 | a0001c0001t0006g0124 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.526+826T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650510 | ||||||
| chr12:98650641
|
A | G | 10 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(7): Show | 10 | HG01081.hp1 HG01109.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+957A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650641 | ||||||
| chr12:98650682
|
C | G | 1 | a0007c0011t0025g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526+998C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650682 | ||||||
| chr12:98650837
|
T | G | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+1153T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650837 | ||||||
| chr12:98650909
|
AAT | A | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+1228_526+1229d others(4): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98650909 | |||||
| chr12:98650978
|
G | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0227a0001c0001t0001g0274others(12): Show | 16 | HG00438.hp2 NA18939.hp1 NA18940.hp1 others(13): Show |
intron_variant | MODIFIER | c.526+1294G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650978 | ||||||
| chr12:98650985
|
C | T | 25 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0257others(22): Show | 25 | HG00140.hp1 HG00544.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.526+1301C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98650985 | ||||||
| chr12:98651142
|
C | T | 86 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(83): Show | 86 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.526+1458C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98651142 | ||||||
| chr12:98651273
|
T | C | 1 | a0001c0001t0002g0324 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.526+1589T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98651273 | ||||||
| chr12:98651388
|
G | A | 1 | a0001c0001t0003g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.526+1704G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98651388 | ||||||
| chr12:98651414
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0274a0001c0001t0001g0275others(2): Show | 6 | HG00438.hp2 NA18961.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+1730G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98651414 | ||||||
| chr12:98651598
|
C | T | 1 | a0001c0001t0037g0299 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.526+1914C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98651598 | ||||||
| chr12:98651664
|
T | A | 1 | a0001c0001t0004g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.526+1980T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98651664 | ||||||
| chr12:98651665
|
TG | T | 30 | a0001c0001t0004g0126a0001c0001t0004g0176a0001c0001t0004g0177others(27): Show | 30 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.526+1982delG | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98651665 | ||||||
| chr12:98651713
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.526+2029G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98651713 | ||||||
| chr12:98651782
|
C | T | 23 | a0001c0001t0001g0294a0001c0001t0010g0291a0001c0001t0010g0292others(20): Show | 23 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.526+2098C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98651782 | ||||||
| chr12:98651982
|
T | A | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.526+2298T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98651982 | ||||||
| chr12:98652034
|
C | G | 6 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(3): Show | 6 | HG01081.hp1 HG01109.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+2350C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98652034 | ||||||
| chr12:98652210
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.526+2526C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98652210 | ||||||
| chr12:98652416
|
G | A | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.526+2732G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98652416 | ||||||
| chr12:98652464
|
A | G | 1 | a0001c0001t0012g0218 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.526+2780A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98652464 | ||||||
| chr12:98652491
|
T | G | 1 | a0001c0001t0004g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.526+2807T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98652491 | ||||||
| chr12:98652584
|
A | G | 10 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(7): Show | 10 | HG01081.hp1 HG01109.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+2900A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98652584 | ||||||
| chr12:98652635
|
A | T | 53 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(50): Show | 53 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.526+2951A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98652635 | ||||||
| chr12:98652687
|
C | T | 1 | a0001c0001t0010g0296 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.526+3003C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98652687 | ||||||
| chr12:98652749
|
T | C | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.526+3065T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98652749 | ||||||
| chr12:98652990
|
C | G | 38 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(35): Show | 38 | HG00408.hp1 HG00438.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.526+3306C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98652990 | ||||||
| chr12:98653137
|
T | A | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.526+3453T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653137 | ||||||
| chr12:98653215
|
A | G | 1 | a0001c0001t0003g0175 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.526+3531A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653215 | ||||||
| chr12:98653473
|
A | G | 1 | a0001c0001t0006g0174 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.526+3789A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653473 | ||||||
| chr12:98653572
|
G | A | 16 | a0001c0001t0001g0294a0001c0001t0010g0291a0001c0001t0010g0292others(13): Show | 16 | HG01433.hp2 HG02257.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.526+3888G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653572 | ||||||
| chr12:98653638
|
C | T | 1 | a0001c0002t0032g0217 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.526+3954C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653638 | ||||||
| chr12:98653651
|
C | T | 13 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(10): Show | 13 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+3967C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653651 | ||||||
| chr12:98653656
|
CA | C | 16 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0120others(13): Show | 16 | HG00140.hp2 HG00544.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.526+4008delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAA | C | 7 | a0001c0001t0001g0207a0001c0001t0001g0274a0001c0001t0004g0191others(4): Show | 7 | HG00280.hp2 HG00438.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.526+4007_526+4008d others(4): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAA | C | 7 | a0001c0001t0001g0251a0001c0001t0001g0294a0001c0001t0007g0250others(4): Show | 7 | HG01081.hp1 HG01433.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.526+4006_526+4008d others(5): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAAA | C | 8 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0003g0134others(5): Show | 8 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+4005_526+4008d others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAAAA | C | 19 | a0001c0001t0003g0125a0001c0001t0003g0154a0001c0001t0003g0168others(16): Show | 19 | HG00735.hp1 HG02071.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.526+4004_526+4008d others(7): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAAAAA | C | 7 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0006g0157others(4): Show | 7 | HG02293.hp1 HG02922.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.526+4003_526+4008d others(8): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAAAAAA | C | 29 | a0001c0001t0003g0141a0001c0001t0003g0143a0001c0001t0003g0144others(26): Show | 29 | HG01192.hp2 HG01346.hp1 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.526+4002_526+4008d others(9): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0004g0180others(3): Show | 6 | HG00408.hp2 HG00558.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+4001_526+4008d others(10): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAAAAAA others(2): Show |
C | 10 | a0001c0001t0003g0158a0001c0001t0004g0178a0001c0001t0004g0189others(7): Show | 10 | HG00738.hp1 HG01109.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+4000_526+4008d others(11): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0004g0179a0001c0001t0012g0218 | 2 | HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.526+3999_526+4008d others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0004g0188a0001c0001t0038g0320 | 2 | HG01433.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.526+3998_526+4008d others(13): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0323 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.526+3997_526+4008d others(14): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAAAAAA others(6): Show |
C | 10 | a0001c0001t0002g0221a0001c0001t0002g0315a0001c0001t0002g0318others(7): Show | 10 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+3996_526+4008d others(15): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0021g0321 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.526+3995_526+4008d others(16): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAAAAAA others(8): Show |
C | 6 | a0001c0001t0002g0316a0001c0001t0002g0317a0001c0001t0002g0344others(3): Show | 6 | HG01069.hp1 HG01071.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+3994_526+4008d others(17): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653656
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0002g0324 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.526+3993_526+4008d others(18): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653656 | |||||
| chr12:98653673
|
A | T | 1 | a0001c0001t0037g0299 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.526+3989A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653673 | ||||||
| chr12:98653675
|
A | T | 1 | a0001c0001t0037g0299 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.526+3991A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653675 | ||||||
| chr12:98653676
|
AAAAAAAA others(10): Show |
A | 23 | a0001c0001t0002g0209a0001c0001t0002g0314a0001c0001t0002g0326others(20): Show | 23 | HG00408.hp1 HG00621.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.526+3994_526+4010d others(19): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653676 | |||||
| chr12:98653677
|
A | T | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.526+3993A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653677 | ||||||
| chr12:98653677
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0002g0325 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.526+3995_526+4012d others(20): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653677 | |||||
| chr12:98653679
|
A | T | 4 | a0001c0001t0001g0097a0001c0001t0004g0192a0001c0001t0036g0300others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+3995A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653679 | ||||||
| chr12:98653679
|
AAAAAAAA others(15): Show |
A | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.526+3997_526+4018d others(24): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653679 | |||||
| chr12:98653680
|
AAAAAAAA others(6): Show |
A | 6 | a0001c0001t0004g0182a0001c0001t0004g0183a0001c0001t0004g0184others(3): Show | 6 | HG02572.hp2 HG02886.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+3998_526+4010d others(15): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653680 | |||||
| chr12:98653680
|
AAAAAAAA others(14): Show |
A | 1 | a0001c0001t0012g0210 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.526+3998_526+4018d others(23): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653680 | |||||
| chr12:98653681
|
A | T | 6 | a0001c0001t0001g0097a0001c0001t0004g0191a0001c0001t0004g0192others(3): Show | 6 | HG00280.hp2 HG01081.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+3997A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653681 | ||||||
| chr12:98653681
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0003g0170 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.526+3999_526+4014d others(18): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653681 | |||||
| chr12:98653682
|
AAAAAAAA others(6): Show |
A | 3 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0205 | 3 | HG02630.hp2 HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.526+4000_526+4012d others(15): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653682 | |||||
| chr12:98653683
|
A | T | 10 | a0001c0001t0001g0097a0001c0001t0004g0191a0001c0001t0004g0192others(7): Show | 10 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.526+3999A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653683 | ||||||
| chr12:98653685
|
A | AATATATA others(3): Show |
2 | a0001c0001t0001g0026a0001c0001t0005g0095 | 2 | HG02280.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.526+4002_526+4003i others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653685 | |||||
| chr12:98653685
|
A | AATATATA others(5): Show |
1 | a0001c0001t0005g0096 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.526+4002_526+4003i others(14): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653685 | |||||
| chr12:98653685
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.526+4002_526+4003i others(16): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653685 | |||||
| chr12:98653685
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0273 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.526+4001_526+4002i others(17): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653685 | ||||||
| chr12:98653685
|
A | T | 19 | a0001c0001t0001g0097a0001c0001t0001g0294a0001c0001t0004g0191others(16): Show | 19 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.526+4001A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653685 | ||||||
| chr12:98653685
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0013g0303 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.526+4003_526+4012d others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653685 | |||||
| chr12:98653685
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0013g0301a0001c0001t0013g0302 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.526+4003_526+4014d others(14): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653685 | |||||
| chr12:98653687
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0015 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.526+4004_526+4005i others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653687 | |||||
| chr12:98653687
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0092 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.526+4004_526+4005i others(18): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653687 | |||||
| chr12:98653687
|
A | AATATATA others(15): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0093 | 2 | HG02056.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.526+4004_526+4005i others(24): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653687 | |||||
| chr12:98653687
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0117 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.526+4003_526+4004i others(13): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653687 | ||||||
| chr12:98653687
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.526+4003_526+4004i others(17): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653687 | ||||||
| chr12:98653687
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0094 | 2 | HG01168.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.526+4003_526+4004i others(19): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653687 | ||||||
| chr12:98653687
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0106 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.526+4003_526+4004i others(23): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653687 | ||||||
| chr12:98653687
|
A | T | 39 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0097others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.526+4003A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653687 | ||||||
| chr12:98653689
|
A | AATATATA others(3): Show |
1 | a0001c0001t0016g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.526+4006_526+4007i others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653689 | |||||
| chr12:98653689
|
A | AATATATA others(5): Show |
4 | a0001c0001t0001g0014a0001c0001t0001g0072a0001c0001t0001g0267others(1): Show | 4 | HG00544.hp1 HG01496.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+4006_526+4007i others(14): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653689 | |||||
| chr12:98653689
|
A | AATATATA others(7): Show |
4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0118others(1): Show | 4 | HG00323.hp1 HG02738.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+4006_526+4007i others(16): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653689 | |||||
| chr12:98653689
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0074 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.526+4006_526+4007i others(18): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653689 | |||||
| chr12:98653689
|
A | AATATATA others(11): Show |
3 | a0001c0001t0001g0021a0001c0001t0005g0075a0001c0001t0005g0076 | 3 | HG01074.hp1 NA18962.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.526+4006_526+4007i others(20): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653689 | |||||
| chr12:98653689
|
A | AATATATA others(15): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0102 | 2 | HG00738.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.526+4006_526+4007i others(24): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653689 | |||||
| chr12:98653689
|
A | ATATATAA others(4): Show |
1 | a0001c0001t0001g0078 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.526+4005_526+4006i others(13): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653689 | ||||||
| chr12:98653689
|
A | ATATATAT others(2): Show |
3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0009g0079 | 3 | HG01361.hp2 HG03017.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.526+4005_526+4006i others(11): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653689 | ||||||
| chr12:98653689
|
A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0022a0001c0001t0001g0271a0001c0001t0005g0080 | 3 | HG01167.hp2 HG01516.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.526+4005_526+4006i others(13): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653689 | ||||||
| chr12:98653689
|
A | ATATATAT others(6): Show |
7 | a0001c0001t0001g0081a0001c0001t0001g0103a0001c0001t0001g0108others(4): Show | 7 | HG00280.hp1 HG00733.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.526+4005_526+4006i others(15): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653689 | ||||||
| chr12:98653689
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0005g0083a0001c0001t0009g0084 | 2 | HG02965.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.526+4005_526+4006i others(17): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653689 | ||||||
| chr12:98653689
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0085a0001c0001t0005g0086 | 2 | HG03492.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.526+4005_526+4006i others(19): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653689 | ||||||
| chr12:98653689
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0005g0087 | 3 | HG03927.hp1 NA18993.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.526+4005_526+4006i others(21): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653689 | ||||||
| chr12:98653689
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0005g0090 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.526+4005_526+4006i others(29): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653689 | ||||||
| chr12:98653689
|
A | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0023others(69): Show | 73 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.526+4005A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653689 | ||||||
| chr12:98653689
|
AAAATATA others(9): Show |
A | 1 | a0001c0001t0001g0265 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.526+4007_526+4022d others(18): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653689 | |||||
| chr12:98653690
|
AAATATAT others(4): Show |
A | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.526+4008_526+4018d others(13): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653690 | |||||
| chr12:98653690
|
AAATATAT others(8): Show |
A | 1 | a0001c0001t0009g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.526+4008_526+4022d others(17): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653690 | |||||
| chr12:98653691
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0001g0027 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.526+4008_526+4009i others(14): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAAAAATA others(9): Show |
1 | a0001c0001t0001g0028 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.526+4008_526+4009i others(18): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAAAAATA others(15): Show |
1 | a0001c0010t0001g0029 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.526+4008_526+4009i others(24): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAAAAATA others(17): Show |
1 | a0001c0001t0001g0030 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.526+4008_526+4009i others(26): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAAAATAT others(10): Show |
1 | a0001c0001t0001g0031 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.526+4008_526+4009i others(19): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAAAATAT others(14): Show |
1 | a0001c0001t0001g0032 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.526+4008_526+4009i others(23): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAAAATAT others(18): Show |
1 | a0001c0001t0001g0119 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.526+4008_526+4009i others(27): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0035 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.526+4008_526+4009i others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAAATATA others(9): Show |
1 | a0001c0001t0001g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.526+4008_526+4009i others(18): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAATATAT others(4): Show |
2 | a0001c0001t0001g0011a0001c0001t0031g0252 | 2 | HG02004.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.526+4008_526+4009i others(13): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAATATAT others(6): Show |
2 | a0001c0001t0001g0111a0001c0001t0001g0113 | 2 | HG02129.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.526+4008_526+4009i others(15): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAATATAT others(8): Show |
1 | a0001c0001t0001g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.526+4008_526+4009i others(17): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAATATAT others(10): Show |
2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG00621.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.526+4008_526+4009i others(19): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAATATAT others(12): Show |
1 | a0001c0001t0001g0039 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.526+4008_526+4009i others(21): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AAATATAT others(18): Show |
1 | a0001c0001t0005g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.526+4008_526+4009i others(27): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0044 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.526+4031_526+4040d others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0254 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.526+4029_526+4040d others(14): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0107 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.526+4027_526+4040d others(16): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AATATATA others(9): Show |
4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0099others(1): Show | 4 | HG02622.hp1 HG03654.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+4025_526+4040d others(18): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AATATATA others(11): Show |
4 | a0001c0001t0001g0049a0001c0001t0001g0100a0001c0001t0001g0114others(1): Show | 4 | HG00735.hp2 HG03831.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+4023_526+4040d others(20): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AATATATA others(13): Show |
1 | a0001c0001t0001g0050 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.526+4021_526+4040d others(22): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0051 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.526+4019_526+4040d others(24): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | AATATATA others(17): Show |
1 | a0001c0001t0005g0109 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.526+4017_526+4040d others(26): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653691
|
A | ACTATATA others(7): Show |
1 | a0001c0001t0001g0234 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.526+4007_526+4008i others(16): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653691 | ||||||
| chr12:98653691
|
A | AT | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0280others(3): Show | 6 | HG02083.hp1 HG03139.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+4007_526+4008i others(3): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653691 | ||||||
| chr12:98653691
|
A | ATATATAT | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0004c0006t0001g0256 | 3 | HG03669.hp1 HG04115.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.526+4007_526+4008i others(9): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653691 | ||||||
| chr12:98653691
|
A | ATATATAT others(2): Show |
3 | a0001c0001t0001g0259a0001c0001t0001g0288a0001c0001t0039g0008 | 3 | HG00140.hp1 HG00741.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.526+4007_526+4008i others(11): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653691 | ||||||
| chr12:98653691
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0260a0004c0006t0001g0356 | 2 | HG01192.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.526+4007_526+4008i others(13): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653691 | ||||||
| chr12:98653691
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0057a0001c0001t0001g0206 | 2 | HG02922.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.526+4007_526+4008i others(15): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653691 | ||||||
| chr12:98653691
|
A | ATATATAT others(8): Show |
9 | a0001c0001t0001g0012a0001c0001t0001g0059a0001c0001t0001g0061others(6): Show | 9 | HG01952.hp2 HG02738.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.526+4007_526+4008i others(17): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653691 | ||||||
| chr12:98653691
|
A | ATATATAT others(10): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0064others(2): Show | 5 | HG01515.hp2 HG01517.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.526+4007_526+4008i others(19): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653691 | ||||||
| chr12:98653691
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0005g0066 | 3 | HG02698.hp2 NA19009.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.526+4007_526+4008i others(21): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653691 | ||||||
| chr12:98653691
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0067 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.526+4007_526+4008i others(23): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653691 | ||||||
| chr12:98653691
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0013 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.526+4007_526+4008i others(27): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653691 | ||||||
| chr12:98653691
|
A | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(160): Show | 164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.526+4007A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653691 | ||||||
| chr12:98653691
|
AATATATA others(3): Show |
A | 1 | a0001c0001t0001g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.526+4031_526+4040d others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98653691 | |||||
| chr12:98653692
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0229 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.526+4009_526+4023d others(17): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653692 | ||||||
| chr12:98653693
|
T | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0357 | 3 | NA18954.hp1 NA19007.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.526+4009T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653693 | ||||||
| chr12:98653695
|
T | A | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.526+4011T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653695 | ||||||
| chr12:98653696
|
A | C | 4 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0233others(1): Show | 4 | HG02723.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+4012A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653696 | ||||||
| chr12:98653698
|
A | C | 1 | a0001c0002t0001g0355 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.526+4014A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653698 | ||||||
| chr12:98653719
|
T | G | 23 | a0001c0001t0001g0294a0001c0001t0010g0291a0001c0001t0010g0292others(20): Show | 23 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.526+4035T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653719 | ||||||
| chr12:98653811
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.526+4127G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653811 | ||||||
| chr12:98653936
|
T | C | 38 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(35): Show | 38 | HG00408.hp1 HG00438.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.526+4252T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653936 | ||||||
| chr12:98653967
|
A | G | 3 | a0001c0001t0012g0212a0001c0001t0033g0213a0008c0009t0012g0211 | 3 | HG02647.hp2 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.526+4283A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98653967 | ||||||
| chr12:98654015
|
G | T | 1 | a0001c0002t0001g0355 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.526+4331G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98654015 | ||||||
| chr12:98654114
|
A | G | 8 | a0001c0001t0002g0221a0001c0001t0002g0315a0001c0001t0002g0316others(5): Show | 8 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+4430A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98654114 | ||||||
| chr12:98654197
|
T | C | 1 | a0007c0011t0025g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526+4513T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98654197 | ||||||
| chr12:98654664
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.527-4496C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98654664 | ||||||
| chr12:98654725
|
G | T | 1 | a0001c0001t0033g0213 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.527-4435G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98654725 | ||||||
| chr12:98654816
|
C | CT | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(101): Show | 106 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.527-4325dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98654816 | |||||
| chr12:98654816
|
C | CTT | 11 | a0001c0001t0001g0043a0001c0001t0001g0117a0001c0001t0008g0305others(8): Show | 11 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.527-4326_527-4325d others(4): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98654816 | |||||
| chr12:98654816
|
CT | C | 55 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0239others(52): Show | 55 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.527-4325delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98654816 | |||||
| chr12:98654816
|
CTT | C | 16 | a0001c0001t0002g0221a0001c0001t0002g0315a0001c0001t0002g0316others(13): Show | 16 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.527-4326_527-4325d others(4): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98654816 | |||||
| chr12:98654821
|
T | C | 1 | a0001c0001t0001g0244 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.527-4339T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98654821 | ||||||
| chr12:98654835
|
T | A | 147 | a0001c0001t0001g0294a0001c0001t0002g0209a0001c0001t0002g0221others(144): Show | 147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.527-4325T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98654835 | ||||||
| chr12:98654876
|
GA | G | 29 | a0001c0001t0002g0209a0001c0001t0002g0314a0001c0001t0002g0324others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.527-4283delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98654876 | ||||||
| chr12:98654899
|
G | T | 5 | a0001c0001t0003g0139a0001c0001t0003g0154a0001c0001t0003g0167others(2): Show | 5 | HG02132.hp2 NA18945.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-4261G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98654899 | ||||||
| chr12:98654974
|
C | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0038others(5): Show | 8 | HG01099.hp2 HG01358.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-4186C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98654974 | ||||||
| chr12:98655299
|
T | C | 49 | a0001c0001t0001g0245a0001c0001t0002g0209a0001c0001t0002g0221others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.527-3861T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655299 | ||||||
| chr12:98655358
|
C | T | 9 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(6): Show | 9 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-3802C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655358 | ||||||
| chr12:98655365
|
G | GTGGCCGG others(120): Show |
1 | a0001c0001t0001g0246 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.527-3751_527-3625d others(129): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98655365 | |||||
| chr12:98655365
|
GTGGCCGG others(120): Show |
G | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.527-3751_527-3625d others(2): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 98655365 | |||||
| chr12:98655435
|
C | A | 5 | a0001c0001t0001g0059a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-3725C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655435 | ||||||
| chr12:98655437
|
G | A | 9 | a0001c0001t0001g0206a0001c0001t0001g0228a0001c0001t0001g0230others(6): Show | 9 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.527-3723G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655437 | ||||||
| chr12:98655444
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.527-3716C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655444 | ||||||
| chr12:98655448
|
C | T | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-3712C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655448 | ||||||
| chr12:98655464
|
C | A | 1 | a0001c0001t0001g0014 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.527-3696C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655464 | ||||||
| chr12:98655469
|
C | A | 1 | a0001c0001t0001g0262 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.527-3691C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655469 | ||||||
| chr12:98655663
|
G | C | 1 | a0001c0001t0003g0130 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.527-3497G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655663 | ||||||
| chr12:98655705
|
C | A | 1 | a0001c0001t0001g0014 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.527-3455C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655705 | ||||||
| chr12:98655725
|
C | G | 1 | a0001c0002t0001g0355 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.527-3435C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655725 | ||||||
| chr12:98655776
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.527-3384C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655776 | ||||||
| chr12:98655847
|
G | A | 1 | a0001c0001t0005g0090 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.527-3313G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655847 | ||||||
| chr12:98655851
|
T | G | 1 | a0001c0001t0006g0174 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.527-3309T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655851 | ||||||
| chr12:98655909
|
G | A | 10 | a0001c0001t0001g0294a0001c0001t0010g0291a0001c0001t0010g0292others(7): Show | 10 | HG01433.hp2 HG02895.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.527-3251G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655909 | ||||||
| chr12:98655984
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0068 | 2 | HG01071.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.527-3176C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98655984 | ||||||
| chr12:98656018
|
T | A | 1 | a0001c0001t0012g0210 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.527-3142T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656018 | ||||||
| chr12:98656034
|
C | T | 2 | a0001c0001t0009g0070a0001c0001t0009g0079 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.527-3126C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656034 | ||||||
| chr12:98656254
|
A | G | 1 | a0001c0002t0032g0217 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.527-2906A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656254 | ||||||
| chr12:98656293
|
A | T | 168 | a0001c0001t0001g0294a0001c0001t0002g0209a0001c0001t0002g0221others(165): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.527-2867A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656293 | ||||||
| chr12:98656314
|
A | G | 1 | a0001c0001t0037g0299 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.527-2846A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656314 | ||||||
| chr12:98656376
|
C | G | 38 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(35): Show | 38 | HG00408.hp1 HG00438.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.527-2784C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656376 | ||||||
| chr12:98656377
|
A | G | 42 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(39): Show | 42 | HG00408.hp1 HG00438.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.527-2783A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656377 | ||||||
| chr12:98656510
|
G | T | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.527-2650G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656510 | ||||||
| chr12:98656538
|
T | A | 5 | a0001c0001t0001g0240a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG02132.hp1 HG02155.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-2622T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656538 | ||||||
| chr12:98656588
|
A | G | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.527-2572A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656588 | ||||||
| chr12:98656608
|
A | G | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.527-2552A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656608 | ||||||
| chr12:98656708
|
G | T | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.527-2452G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656708 | ||||||
| chr12:98656831
|
G | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | HG00280.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.527-2329G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656831 | ||||||
| chr12:98656865
|
C | T | 2 | a0001c0001t0004g0180a0001c0001t0004g0181 | 2 | HG01258.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.527-2295C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656865 | ||||||
| chr12:98656867
|
G | T | 1 | a0001c0001t0030g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.527-2293G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98656867 | ||||||
| chr12:98657342
|
T | C | 1 | a0001c0001t0002g0344 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.527-1818T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98657342 | ||||||
| chr12:98657406
|
G | C | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-1754G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98657406 | ||||||
| chr12:98657414
|
A | G | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.527-1746A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98657414 | ||||||
| chr12:98657428
|
G | C | 1 | a0001c0001t0012g0210 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.527-1732G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98657428 | ||||||
| chr12:98657451
|
G | A | 1 | a0001c0001t0005g0075 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.527-1709G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98657451 | ||||||
| chr12:98657596
|
A | T | 38 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(35): Show | 38 | HG00408.hp1 HG00438.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.527-1564A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98657596 | ||||||
| chr12:98657862
|
A | G | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-1298A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98657862 | ||||||
| chr12:98657922
|
T | C | 1 | a0001c0001t0037g0299 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.527-1238T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98657922 | ||||||
| chr12:98658147
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.527-1013G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98658147 | ||||||
| chr12:98658378
|
C | T | 1 | a0007c0011t0025g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.527-782C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98658378 | ||||||
| chr12:98658380
|
C | T | 1 | a0007c0011t0025g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.527-780C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98658380 | ||||||
| chr12:98658529
|
A | G | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.527-631A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98658529 | ||||||
| chr12:98658617
|
A | G | 1 | a0001c0001t0033g0213 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.527-543A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98658617 | ||||||
| chr12:98658639
|
G | A | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG00140.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.527-521G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98658639 | ||||||
| chr12:98658717
|
T | A | 1 | a0001c0001t0010g0295 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.527-443T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98658717 | ||||||
| chr12:98658856
|
A | C | 38 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(35): Show | 38 | HG00408.hp1 HG00438.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.527-304A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98658856 | ||||||
| chr12:98658876
|
C | A | 2 | a0002c0003t0007g0353a0002c0003t0007g0354 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.527-284C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98658876 | ||||||
| chr12:98658919
|
G | A | 1 | a0001c0001t0012g0210 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.527-241G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98658919 | ||||||
| chr12:98659025
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.527-135T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98659025 | ||||||
| chr12:98659032
|
C | T | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.527-128C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98659032 | ||||||
| chr12:98659102
|
C | T | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.527-58C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 4/26 | chr12 | 98659102 | ||||||
| chr12:98659438
|
G | C | 10 | a0001c0001t0001g0206a0001c0001t0001g0228a0001c0001t0001g0230others(7): Show | 10 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.710+95G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98659438 | ||||||
| chr12:98659517
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.710+174C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98659517 | ||||||
| chr12:98659752
|
G | GA | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.710+429dupA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr12 | 98659752 | |||||
| chr12:98659752
|
G | GAA | 14 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0116others(11): Show | 14 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.710+428_710+429dup others(2): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr12 | 98659752 | |||||
| chr12:98659752
|
G | GAAA | 20 | a0001c0001t0002g0221a0001c0001t0002g0314a0001c0001t0002g0324others(17): Show | 20 | HG00438.hp1 HG02080.hp2 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.710+427_710+429dup others(3): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr12 | 98659752 | |||||
| chr12:98659752
|
G | GAAAA | 8 | a0001c0001t0002g0209a0001c0001t0002g0325a0001c0001t0002g0327others(5): Show | 8 | HG00408.hp1 HG00621.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.710+426_710+429dup others(4): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr12 | 98659752 | |||||
| chr12:98659752
|
GA | G | 9 | a0001c0001t0001g0294a0001c0001t0010g0291a0001c0001t0010g0295others(6): Show | 9 | HG01433.hp2 HG02895.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.710+429delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr12 | 98659752 | |||||
| chr12:98659770
|
AAAGAG | A | 6 | a0001c0001t0008g0308a0001c0001t0008g0311a0001c0001t0008g0312others(3): Show | 6 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.710+429_710+433del others(5): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr12 | 98659770 | |||||
| chr12:98659771
|
A | AG | 5 | a0001c0001t0001g0050a0001c0001t0001g0105a0001c0001t0005g0062others(2): Show | 5 | HG02572.hp1 HG02602.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.710+428_710+429ins others(1): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98659771 | ||||||
| chr12:98659771
|
A | G | 1 | a0001c0002t0001g0355 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.710+428A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98659771 | ||||||
| chr12:98659776
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.710+433A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98659776 | ||||||
| chr12:98659781
|
A | G | 9 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(6): Show | 9 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.710+438A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98659781 | ||||||
| chr12:98659835
|
A | C | 1 | a0001c0001t0006g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.710+492A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98659835 | ||||||
| chr12:98659916
|
T | C | 1 | a0001c0001t0027g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.710+573T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98659916 | ||||||
| chr12:98659985
|
A | C | 1 | a0001c0001t0016g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.710+642A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98659985 | ||||||
| chr12:98660540
|
T | A | 9 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0182others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.710+1197T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98660540 | ||||||
| chr12:98660604
|
C | A | 1 | a0001c0001t0004g0190 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.710+1261C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98660604 | ||||||
| chr12:98660705
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.710+1362G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98660705 | ||||||
| chr12:98660726
|
A | G | 1 | a0001c0001t0019g0215 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.710+1383A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98660726 | ||||||
| chr12:98661008
|
T | G | 1 | a0001c0001t0010g0291 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.711-1448T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661008 | ||||||
| chr12:98661091
|
T | C | 50 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.711-1365T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661091 | ||||||
| chr12:98661092
|
G | A | 50 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.711-1364G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661092 | ||||||
| chr12:98661093
|
A | G | 50 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.711-1363A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661093 | ||||||
| chr12:98661109
|
A | G | 60 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.711-1347A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661109 | ||||||
| chr12:98661128
|
C | G | 1 | a0001c0001t0012g0218 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.711-1328C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661128 | ||||||
| chr12:98661344
|
T | C | 3 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0273 | 3 | HG00544.hp1 NA18747.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.711-1112T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661344 | ||||||
| chr12:98661381
|
G | T | 1 | a0001c0001t0001g0012 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.711-1075G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661381 | ||||||
| chr12:98661421
|
G | A | 63 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.711-1035G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661421 | ||||||
| chr12:98661536
|
G | T | 1 | a0001c0001t0006g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.711-920G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661536 | ||||||
| chr12:98661537
|
T | C | 1 | a0001c0001t0006g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.711-919T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661537 | ||||||
| chr12:98661649
|
A | G | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.711-807A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661649 | ||||||
| chr12:98661826
|
C | T | 6 | a0001c0001t0036g0300a0001c0001t0037g0299a0001c0004t0007g0225others(3): Show | 6 | HG01081.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.711-630C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661826 | ||||||
| chr12:98661894
|
C | T | 63 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.711-562C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661894 | ||||||
| chr12:98661901
|
C | T | 63 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.711-555C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661901 | ||||||
| chr12:98661944
|
A | T | 1 | a0001c0001t0006g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.711-512A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98661944 | ||||||
| chr12:98662096
|
G | A | 1 | a0001c0001t0036g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.711-360G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98662096 | ||||||
| chr12:98662107
|
A | C | 1 | a0001c0001t0012g0218 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.711-349A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98662107 | ||||||
| chr12:98662145
|
C | T | 4 | a0001c0001t0036g0300a0001c0001t0037g0299a0003c0005t0007g0219others(1): Show | 4 | HG01081.hp1 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-311C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98662145 | ||||||
| chr12:98662147
|
C | CT | 8 | a0001c0001t0001g0054a0001c0001t0001g0089a0001c0001t0001g0114others(5): Show | 8 | HG03831.hp2 HG03927.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.711-291dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr12 | 98662147 | |||||
| chr12:98662147
|
CT | C | 12 | a0001c0001t0002g0323a0001c0001t0012g0210a0001c0001t0013g0301others(9): Show | 12 | HG01081.hp1 HG01109.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.711-291delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr12 | 98662147 | |||||
| chr12:98662147
|
CTT | C | 52 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(49): Show | 52 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.711-292_711-291del others(2): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr12 | 98662147 | |||||
| chr12:98662257
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.711-199A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98662257 | ||||||
| chr12:98662299
|
T | C | 8 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(5): Show | 8 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.711-157T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98662299 | ||||||
| chr12:98662308
|
G | A | 30 | a0001c0001t0004g0126a0001c0001t0004g0176a0001c0001t0004g0177others(27): Show | 30 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.711-148G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98662308 | ||||||
| chr12:98662316
|
C | T | 1 | a0001c0001t0012g0218 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.711-140C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98662316 | ||||||
| chr12:98662347
|
T | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.711-109T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98662347 | ||||||
| chr12:98662385
|
G | T | 1 | a0001c0001t0006g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.711-71G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98662385 | ||||||
| chr12:98662386
|
T | G | 1 | a0001c0001t0006g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.711-70T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98662386 | ||||||
| chr12:98662387
|
G | T | 1 | a0001c0001t0006g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.711-69G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98662387 | ||||||
| chr12:98662440
|
T | A | 1 | a0001c0001t0003g0131 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.711-16T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 5/26 | chr12 | 98662440 | ||||||
| chr12:98662581
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0287 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.823+13C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 6/26 | chr12 | 98662581 | ||||||
| chr12:98663074
|
T | C | 63 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.955+268T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98663074 | ||||||
| chr12:98663081
|
A | C | 9 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0182others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.955+275A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98663081 | ||||||
| chr12:98663143
|
T | C | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.955+337T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98663143 | ||||||
| chr12:98663207
|
T | C | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.955+401T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98663207 | ||||||
| chr12:98663331
|
A | G | 4 | a0001c0001t0012g0212a0001c0001t0012g0218a0001c0001t0033g0213others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+525A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98663331 | ||||||
| chr12:98663460
|
T | A | 1 | a0001c0001t0006g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.955+654T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98663460 | ||||||
| chr12:98663536
|
C | T | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.955+730C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98663536 | ||||||
| chr12:98663720
|
G | T | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0053others(2): Show | 5 | NA18954.hp1 NA18973.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.955+914G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98663720 | ||||||
| chr12:98663950
|
A | G | 1 | a0001c0001t0004g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.955+1144A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98663950 | ||||||
| chr12:98664233
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.956-1320A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98664233 | ||||||
| chr12:98664510
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.956-1043A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98664510 | ||||||
| chr12:98664524
|
T | C | 1 | a0001c0001t0005g0095 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.956-1029T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98664524 | ||||||
| chr12:98664541
|
C | CT | 6 | a0001c0001t0001g0240a0001c0001t0001g0244a0001c0001t0001g0245others(3): Show | 6 | HG02132.hp1 HG02155.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.956-1002dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98664541 | |||||
| chr12:98664560
|
A | G | 1 | a0001c0001t0005g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.956-993A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98664560 | ||||||
| chr12:98664686
|
AC | A | 4 | a0001c0001t0015g0127a0001c0001t0015g0128a0001c0001t0015g0129others(1): Show | 4 | HG01891.hp2 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.956-865delC | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98664686 | |||||
| chr12:98664807
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.956-746C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98664807 | ||||||
| chr12:98664822
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0287 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.956-731G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98664822 | ||||||
| chr12:98664906
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.956-647A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98664906 | ||||||
| chr12:98664914
|
A | G | 1 | a0002c0003t0007g0354 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.956-639A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98664914 | ||||||
| chr12:98665186
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0289a0001c0001t0001g0290 | 4 | HG00642.hp1 HG00733.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-367C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665186 | ||||||
| chr12:98665245
|
T | C | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.956-308T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665245 | ||||||
| chr12:98665255
|
C | CACATATA others(23): Show |
1 | a0001c0001t0003g0158 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.956-297_956-296ins others(30): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CAT | 5 | a0001c0001t0001g0359a0001c0001t0001g0361a0001c0001t0001g0362others(2): Show | 5 | HG01069.hp2 HG01515.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.956-275_956-274dup others(2): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CATATAT | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-279_956-274dup others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CATATATA others(3): Show |
1 | a0001c0002t0023g0309 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.956-283_956-274dup others(10): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CATATATA others(5): Show |
1 | a0001c0002t0032g0217 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.956-285_956-274dup others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CATATATA others(11): Show |
1 | a0001c0001t0003g0159 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.956-291_956-274dup others(18): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CATATATA others(13): Show |
7 | a0001c0001t0003g0141a0001c0001t0003g0146a0001c0001t0003g0147others(4): Show | 7 | HG02129.hp2 NA18945.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.956-293_956-274dup others(20): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CATATATA others(15): Show |
3 | a0001c0001t0003g0170a0001c0001t0015g0127a0001c0001t0015g0128 | 3 | HG02451.hp1 HG02523.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.956-295_956-274dup others(22): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CATATATA others(17): Show |
3 | a0001c0001t0003g0155a0001c0001t0030g0007a0007c0011t0025g0204 | 3 | HG00408.hp2 HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.956-297_956-274dup others(24): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CATATATA others(19): Show |
2 | a0001c0001t0003g0133a0001c0001t0004g0189 | 2 | HG03688.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.956-274_956-273ins others(26): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CATATATA others(21): Show |
2 | a0001c0001t0003g0143a0001c0001t0003g0152 | 2 | HG02145.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.956-274_956-273ins others(28): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CATATATA others(23): Show |
5 | a0001c0001t0003g0131a0001c0001t0003g0136a0001c0001t0003g0137others(2): Show | 5 | HG03927.hp2 NA18942.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-274_956-273ins others(30): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CATATATA others(25): Show |
1 | a0001c0001t0011g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.956-274_956-273ins others(32): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CATATATA others(27): Show |
3 | a0001c0001t0003g0134a0001c0001t0026g0151a0005c0008t0011g0142 | 3 | HG01192.hp2 NA19009.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.956-274_956-273ins others(34): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
C | CATATATA others(31): Show |
3 | a0001c0001t0003g0130a0001c0001t0011g0132a0001c0001t0011g0140 | 3 | NA18975.hp2 NA18987.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.956-274_956-273ins others(38): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
CAT | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(122): Show | 126 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.956-275_956-274del others(2): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665255
|
CATAT | C | 8 | a0001c0001t0002g0221a0001c0001t0002g0315a0001c0001t0002g0316others(5): Show | 8 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.956-277_956-274del others(4): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665255 | |||||
| chr12:98665274
|
A | T | 1 | a0001c0001t0001g0240 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.956-279A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665274 | ||||||
| chr12:98665274
|
ATATAT | A | 44 | a0001c0001t0002g0209a0001c0001t0002g0314a0001c0001t0002g0324others(41): Show | 44 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.956-277_956-273del others(5): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665274 | |||||
| chr12:98665275
|
TATA | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0057a0001c0001t0001g0230 | 3 | HG00323.hp1 NA18522.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.956-277_956-275del others(3): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665275 | ||||||
| chr12:98665276
|
A | ATTTTTT | 7 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(4): Show | 7 | HG02895.hp2 HG02897.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.956-276_956-275ins others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665276 | |||||
| chr12:98665276
|
A | T | 12 | a0001c0001t0001g0113a0001c0001t0001g0228a0001c0001t0001g0240others(9): Show | 12 | HG00735.hp1 HG01884.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.956-277A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665276 | ||||||
| chr12:98665277
|
TA | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0067a0001c0001t0001g0074others(7): Show | 11 | HG00642.hp1 HG00733.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.956-275delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665277 | ||||||
| chr12:98665278
|
A | ATATATAT others(2): Show |
8 | a0001c0001t0004g0176a0001c0001t0004g0182a0001c0001t0004g0183others(5): Show | 8 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.956-274_956-273ins others(9): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | ATATATAT others(4): Show |
3 | a0001c0001t0004g0187a0001c0001t0004g0193a0001c0001t0004g0194 | 3 | HG02109.hp1 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.956-274_956-273ins others(11): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0003g0149 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.956-274_956-273ins others(15): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | ATATATAT others(16): Show |
3 | a0001c0001t0004g0178a0001c0001t0004g0179a0001c0001t0004g0181 | 3 | HG01168.hp2 HG01169.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.956-274_956-273ins others(23): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0004g0190 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.956-274_956-273ins others(25): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | ATATATAT others(20): Show |
4 | a0001c0001t0003g0125a0001c0001t0003g0173a0001c0001t0004g0195others(1): Show | 4 | HG01255.hp1 HG02071.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-274_956-273ins others(27): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | ATATATAT others(22): Show |
2 | a0001c0001t0004g0199a0001c0001t0015g0129 | 2 | HG03017.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.956-274_956-273ins others(29): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | ATATATAT others(26): Show |
2 | a0001c0001t0004g0196a0001c0001t0004g0197 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.956-274_956-273ins others(33): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | ATATATAT others(23): Show |
2 | a0001c0001t0003g0144a0001c0001t0003g0145 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.956-274_956-273ins others(30): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0003g0156 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.956-274_956-273ins others(24): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0003g0154 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.956-274_956-273ins others(20): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0035g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.956-274_956-273ins others(19): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | ATATATAT others(5): Show |
1 | a0001c0002t0001g0355 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.956-274_956-273ins others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | ATATATAT others(3): Show |
2 | a0002c0003t0007g0353a0002c0003t0007g0354 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.956-274_956-273ins others(10): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
A | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(87): Show | 91 | HG00621.hp1 HG00639.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.956-275A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665278 | ||||||
| chr12:98665278
|
AT | A | 10 | a0001c0001t0001g0089a0001c0001t0001g0098a0001c0001t0001g0101others(7): Show | 10 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.956-260delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665278
|
ATT | A | 7 | a0001c0001t0001g0254a0001c0001t0001g0298a0001c0001t0009g0070others(4): Show | 7 | HG02572.hp1 HG02738.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.956-261_956-260del others(2): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 98665278 | |||||
| chr12:98665279
|
T | TA | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0118others(3): Show | 6 | HG00735.hp2 HG01255.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.956-274_956-273ins others(1): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665279 | ||||||
| chr12:98665279
|
T | TATATATA others(14): Show |
2 | a0001c0001t0003g0139a0001c0001t0004g0180 | 2 | HG01258.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.956-274_956-273ins others(21): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665279 | ||||||
| chr12:98665279
|
T | TATATATA others(20): Show |
1 | a0001c0001t0004g0191 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.956-274_956-273ins others(27): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665279 | ||||||
| chr12:98665280
|
T | A | 19 | a0001c0001t0001g0207a0001c0001t0001g0239a0001c0001t0001g0286others(16): Show | 19 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.956-273T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665280 | ||||||
| chr12:98665281
|
T | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0103a0001c0001t0001g0106 | 3 | HG00280.hp1 HG01361.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.956-272T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665281 | ||||||
| chr12:98665282
|
T | A | 6 | a0001c0001t0003g0130a0001c0001t0003g0134a0001c0001t0011g0140others(3): Show | 6 | HG01891.hp2 HG02451.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.956-271T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665282 | ||||||
| chr12:98665284
|
T | A | 1 | a0001c0001t0011g0140 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.956-269T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665284 | ||||||
| chr12:98665349
|
C | T | 4 | a0001c0001t0001g0098a0001c0001t0001g0101a0001c0001t0001g0104others(1): Show | 4 | HG00741.hp2 HG02083.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-204C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665349 | ||||||
| chr12:98665359
|
C | T | 166 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(163): Show | 166 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.956-194C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665359 | ||||||
| chr12:98665480
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0287 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.956-73A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 7/26 | chr12 | 98665480 | ||||||
| chr12:98665911
|
G | A | 7 | a0001c0001t0002g0221a0001c0001t0002g0315a0001c0001t0002g0316others(4): Show | 7 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1194+120G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 8/26 | chr12 | 98665911 | ||||||
| chr12:98666105
|
G | A | 8 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(5): Show | 8 | HG02895.hp2 HG02897.hp2 HG04228.hp1 others(5): Show |
intron_variant | MODIFIER | c.1195-85G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 8/26 | chr12 | 98666105 | ||||||
| chr12:98666122
|
A | G | 71 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(68): Show | 71 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1195-68A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 8/26 | chr12 | 98666122 | ||||||
| chr12:98666140
|
C | A | 1 | a0001c0001t0002g0326 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1195-50C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 8/26 | chr12 | 98666140 | ||||||
| chr12:98666453
|
A | G | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1362+96A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | chr12 | 98666453 | ||||||
| chr12:98666572
|
A | G | 166 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(163): Show | 166 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1362+215A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | chr12 | 98666572 | ||||||
| chr12:98666849
|
GTTT | G | 70 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(67): Show | 70 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1362+495_1362+497d others(5): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr12 | 98666849 | |||||
| chr12:98667035
|
G | A | 67 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(64): Show | 67 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1363-478G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | chr12 | 98667035 | ||||||
| chr12:98667098
|
G | GTA | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1363-405_1363-404d others(4): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr12 | 98667098 | |||||
| chr12:98667110
|
G | A | 1 | a0001c0001t0002g0315 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1363-403G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | chr12 | 98667110 | ||||||
| chr12:98667112
|
A | G | 1 | a0001c0001t0002g0315 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1363-401A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | chr12 | 98667112 | ||||||
| chr12:98667112
|
A | T | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1363-401A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | chr12 | 98667112 | ||||||
| chr12:98667196
|
G | A | 1 | a0001c0001t0001g0357 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1363-317G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | chr12 | 98667196 | ||||||
| chr12:98667197
|
G | A | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.1363-316G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | chr12 | 98667197 | ||||||
| chr12:98667368
|
G | C | 4 | a0001c0001t0012g0212a0001c0001t0012g0218a0001c0001t0033g0213others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1363-145G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | chr12 | 98667368 | ||||||
| chr12:98667483
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1363-30T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | chr12 | 98667483 | ||||||
| chr12:98667497
|
T | C | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1363-16T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 9/26 | chr12 | 98667497 | ||||||
| chr12:98667765
|
A | AT | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(142): Show | 147 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1494+145dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr12 | 98667765 | |||||
| chr12:98667765
|
A | ATT | 67 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0020others(64): Show | 67 | HG00323.hp2 HG00621.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1494+144_1494+145d others(4): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr12 | 98667765 | |||||
| chr12:98667765
|
A | ATTT | 16 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0328others(13): Show | 16 | HG00408.hp1 HG00438.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.1494+143_1494+145d others(5): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr12 | 98667765 | |||||
| chr12:98667765
|
AT | A | 25 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(22): Show | 25 | HG00735.hp1 HG01081.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1494+145delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr12 | 98667765 | |||||
| chr12:98667822
|
A | T | 3 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303 | 3 | HG01884.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1494+178A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98667822 | ||||||
| chr12:98667887
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1494+243C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98667887 | ||||||
| chr12:98668079
|
T | C | 3 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303 | 3 | HG01884.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1494+435T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98668079 | ||||||
| chr12:98668128
|
C | T | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1494+484C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98668128 | ||||||
| chr12:98668236
|
T | G | 1 | a0001c0001t0003g0139 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1494+592T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98668236 | ||||||
| chr12:98668237
|
G | T | 1 | a0001c0001t0003g0139 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1494+593G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98668237 | ||||||
| chr12:98668611
|
A | T | 9 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(6): Show | 9 | HG02895.hp2 HG02897.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1494+967A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98668611 | ||||||
| chr12:98668641
|
G | A | 5 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0182others(2): Show | 5 | HG02630.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1494+997G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98668641 | ||||||
| chr12:98668705
|
C | T | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1494+1061C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98668705 | ||||||
| chr12:98668880
|
A | T | 1 | a0001c0001t0003g0139 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1494+1236A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98668880 | ||||||
| chr12:98668900
|
A | G | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.1494+1256A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98668900 | ||||||
| chr12:98669092
|
A | G | 17 | a0001c0001t0001g0061a0001c0001t0005g0040a0001c0001t0005g0048others(14): Show | 17 | NA18939.hp2 NA18945.hp1 NA18962.hp1 others(14): Show |
intron_variant | MODIFIER | c.1494+1448A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98669092 | ||||||
| chr12:98669386
|
A | G | 13 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(10): Show | 13 | HG02647.hp2 HG02717.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.1495-1587A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98669386 | ||||||
| chr12:98669400
|
A | G | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1495-1573A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98669400 | ||||||
| chr12:98669687
|
G | A | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1495-1286G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98669687 | ||||||
| chr12:98669884
|
CCCCTCCC others(9): Show |
C | 5 | a0001c0001t0004g0191a0001c0001t0013g0301a0001c0001t0013g0302others(2): Show | 5 | HG00280.hp2 HG01109.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1495-1052_1495-103 others(20): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr12 | 98669884 | |||||
| chr12:98669991
|
G | A | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1495-982G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98669991 | ||||||
| chr12:98670028
|
G | A | 1 | a0001c0001t0004g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1495-945G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98670028 | ||||||
| chr12:98670065
|
C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1495-908C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98670065 | ||||||
| chr12:98670068
|
C | T | 1 | a0001c0001t0004g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1495-905C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98670068 | ||||||
| chr12:98670554
|
G | C | 63 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1495-419G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98670554 | ||||||
| chr12:98670616
|
C | T | 1 | a0001c0001t0002g0340 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1495-357C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98670616 | ||||||
| chr12:98670729
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1495-244G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98670729 | ||||||
| chr12:98670798
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1495-175T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98670798 | ||||||
| chr12:98670882
|
G | A | 1 | a0001c0004t0007g0225 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1495-91G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 10/26 | chr12 | 98670882 | ||||||
| chr12:98671130
|
A | AT | 8 | a0001c0001t0002g0221a0001c0001t0002g0315a0001c0001t0002g0316others(5): Show | 8 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1608+53dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr12 | 98671130 | |||||
| chr12:98671243
|
C | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0108others(3): Show | 6 | HG03098.hp2 HG03130.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1608+157C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 11/26 | chr12 | 98671243 | ||||||
| chr12:98671755
|
G | A | 15 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(12): Show | 15 | HG02257.hp2 HG02647.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1793+36G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98671755 | ||||||
| chr12:98671792
|
G | C | 1 | a0001c0001t0001g0021 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1793+73G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98671792 | ||||||
| chr12:98672153
|
T | TTTTA | 117 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(114): Show | 118 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.1793+458_1793+461d others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 98672153 | |||||
| chr12:98672153
|
TTTTA | T | 158 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(155): Show | 158 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1793+458_1793+461d others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 98672153 | |||||
| chr12:98672257
|
C | T | 1 | a0007c0011t0025g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1793+538C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98672257 | ||||||
| chr12:98672272
|
C | G | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1793+553C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98672272 | ||||||
| chr12:98672316
|
C | G | 1 | a0001c0001t0001g0270 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1793+597C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98672316 | ||||||
| chr12:98672417
|
G | C | 4 | a0001c0001t0015g0127a0001c0001t0015g0128a0001c0001t0015g0129others(1): Show | 4 | HG01891.hp2 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1793+698G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98672417 | ||||||
| chr12:98672559
|
A | T | 1 | a0001c0001t0007g0065 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1793+840A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98672559 | ||||||
| chr12:98672723
|
A | C | 1 | a0001c0001t0006g0322 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1793+1004A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98672723 | ||||||
| chr12:98672736
|
A | C | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1793+1017A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98672736 | ||||||
| chr12:98672817
|
C | T | 5 | a0001c0001t0003g0152a0001c0001t0013g0301a0001c0001t0013g0302others(2): Show | 5 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1793+1098C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98672817 | ||||||
| chr12:98672916
|
G | C | 1 | a0001c0001t0039g0008 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1793+1197G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98672916 | ||||||
| chr12:98673252
|
G | A | 3 | a0001c0001t0010g0292a0001c0001t0010g0296a0001c0001t0010g0297 | 3 | NA18940.hp2 NA18952.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1793+1533G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98673252 | ||||||
| chr12:98673416
|
A | G | 63 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1793+1697A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98673416 | ||||||
| chr12:98673442
|
C | CA | 61 | a0001c0001t0001g0119a0001c0001t0001g0359a0001c0001t0002g0209others(58): Show | 61 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1793+1737dupA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 98673442 | |||||
| chr12:98673457
|
C | A | 13 | a0001c0001t0001g0011a0001c0001t0008g0305a0001c0001t0008g0306others(10): Show | 13 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1793+1738C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98673457 | ||||||
| chr12:98673461
|
A | C | 3 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303 | 3 | HG01884.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1793+1742A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98673461 | ||||||
| chr12:98673468
|
C | A | 8 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(5): Show | 8 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1793+1749C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98673468 | ||||||
| chr12:98673541
|
A | G | 2 | a0001c0001t0014g0122a0001c0001t0014g0123 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1793+1822A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98673541 | ||||||
| chr12:98673600
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0289a0001c0001t0001g0290 | 4 | HG00642.hp1 HG00733.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1793+1881A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98673600 | ||||||
| chr12:98673764
|
G | A | 13 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(10): Show | 13 | HG02647.hp2 HG02717.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.1793+2045G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98673764 | ||||||
| chr12:98673812
|
G | A | 167 | a0001c0001t0001g0121a0001c0001t0002g0209a0001c0001t0002g0221others(164): Show | 167 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1793+2093G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98673812 | ||||||
| chr12:98673941
|
A | T | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1793+2222A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98673941 | ||||||
| chr12:98674128
|
T | C | 15 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(12): Show | 15 | HG02257.hp2 HG02647.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1793+2409T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98674128 | ||||||
| chr12:98674141
|
A | C | 1 | a0001c0001t0002g0323 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1793+2422A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98674141 | ||||||
| chr12:98674269
|
G | A | 1 | a0001c0001t0005g0082 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1793+2550G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98674269 | ||||||
| chr12:98674312
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1793+2593A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98674312 | ||||||
| chr12:98674332
|
A | G | 4 | a0001c0001t0012g0212a0001c0001t0012g0218a0001c0001t0033g0213others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1793+2613A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98674332 | ||||||
| chr12:98674408
|
C | T | 1 | a0001c0001t0010g0291 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1793+2689C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98674408 | ||||||
| chr12:98674439
|
G | GTC | 71 | a0001c0001t0001g0121a0001c0001t0002g0341a0001c0001t0003g0125others(68): Show | 71 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1793+2742_1793+274 others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 98674439 | |||||
| chr12:98674463
|
G | C | 1 | a0001c0001t0008g0308 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1793+2744G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98674463 | ||||||
| chr12:98674543
|
T | C | 1 | a0001c0001t0034g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1793+2824T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98674543 | ||||||
| chr12:98674705
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0227a0001c0001t0001g0274others(4): Show | 8 | HG00438.hp2 NA18940.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.1794-2720G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98674705 | ||||||
| chr12:98674792
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1794-2633G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98674792 | ||||||
| chr12:98674814
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1794-2611T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98674814 | ||||||
| chr12:98675005
|
C | G | 5 | a0001c0002t0001g0355a0001c0002t0023g0309a0001c0002t0032g0217others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1794-2420C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98675005 | ||||||
| chr12:98675198
|
G | A | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1794-2227G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98675198 | ||||||
| chr12:98675272
|
A | T | 1 | a0001c0001t0003g0156 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1794-2153A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98675272 | ||||||
| chr12:98675380
|
A | T | 2 | a0002c0003t0007g0353a0002c0003t0007g0354 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1794-2045A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98675380 | ||||||
| chr12:98675415
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1794-2010C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98675415 | ||||||
| chr12:98675546
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1794-1879T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98675546 | ||||||
| chr12:98675630
|
T | C | 8 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(5): Show | 8 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1794-1795T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98675630 | ||||||
| chr12:98675964
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0289a0001c0001t0001g0290 | 4 | HG00642.hp1 HG00733.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1794-1461C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98675964 | ||||||
| chr12:98676071
|
C | T | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1794-1354C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98676071 | ||||||
| chr12:98676141
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1794-1284G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98676141 | ||||||
| chr12:98676335
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0112 | 2 | HG00558.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1794-1090G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98676335 | ||||||
| chr12:98676400
|
G | A | 1 | a0001c0001t0020g0352 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1794-1025G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98676400 | ||||||
| chr12:98676456
|
G | A | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG00140.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1794-969G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98676456 | ||||||
| chr12:98676650
|
G | GT | 321 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(318): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1794-761dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 98676650 | |||||
| chr12:98676780
|
G | T | 4 | a0001c0001t0012g0212a0001c0001t0012g0218a0001c0001t0033g0213others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794-645G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98676780 | ||||||
| chr12:98676793
|
C | T | 4 | a0001c0001t0036g0300a0001c0001t0037g0299a0003c0005t0007g0219others(1): Show | 4 | HG01081.hp1 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794-632C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98676793 | ||||||
| chr12:98677065
|
A | G | 97 | a0001c0001t0001g0011a0001c0001t0001g0121a0001c0001t0003g0125others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1794-360A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98677065 | ||||||
| chr12:98677245
|
T | C | 73 | a0001c0001t0001g0011a0001c0001t0001g0121a0001c0001t0003g0125others(70): Show | 73 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1794-180T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98677245 | ||||||
| chr12:98677292
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1794-133T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98677292 | ||||||
| chr12:98677321
|
G | A | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1794-104G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98677321 | ||||||
| chr12:98677387
|
A | G | 4 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0017g0202others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794-38A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98677387 | ||||||
| chr12:98677406
|
A | G | 1 | a0001c0001t0004g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1794-19A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 12/26 | chr12 | 98677406 | ||||||
| chr12:98677903
|
A | G | 51 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(48): Show | 51 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1920+352A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98677903 | ||||||
| chr12:98678035
|
T | G | 1 | a0001c0001t0001g0051 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1920+484T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98678035 | ||||||
| chr12:98678114
|
C | T | 15 | a0001c0001t0004g0126a0001c0001t0004g0176a0001c0001t0004g0177others(12): Show | 15 | HG00639.hp2 HG01257.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1920+563C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98678114 | ||||||
| chr12:98678303
|
G | A | 61 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(58): Show | 61 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1920+752G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98678303 | ||||||
| chr12:98678411
|
C | T | 1 | a0001c0001t0002g0319 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1920+860C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98678411 | ||||||
| chr12:98678454
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1920+903C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98678454 | ||||||
| chr12:98678455
|
G | A | 73 | a0001c0001t0001g0011a0001c0001t0001g0121a0001c0001t0003g0125others(70): Show | 73 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1920+904G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98678455 | ||||||
| chr12:98678551
|
C | T | 1 | a0001c0001t0010g0291 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1920+1000C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98678551 | ||||||
| chr12:98678599
|
G | C | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1920+1048G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98678599 | ||||||
| chr12:98678796
|
T | C | 51 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(48): Show | 51 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1920+1245T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98678796 | ||||||
| chr12:98678832
|
C | T | 1 | a0001c0001t0002g0315 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1920+1281C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98678832 | ||||||
| chr12:98678873
|
G | A | 1 | a0001c0001t0031g0252 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1920+1322G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98678873 | ||||||
| chr12:98678885
|
A | G | 1 | a0001c0001t0009g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1920+1334A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98678885 | ||||||
| chr12:98678942
|
A | C | 1 | a0001c0001t0003g0175 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1921-1335A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98678942 | ||||||
| chr12:98679081
|
C | G | 55 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(52): Show | 55 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1921-1196C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679081 | ||||||
| chr12:98679096
|
A | G | 328 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1921-1181A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679096 | ||||||
| chr12:98679169
|
A | G | 15 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(12): Show | 15 | HG02257.hp2 HG02647.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1921-1108A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679169 | ||||||
| chr12:98679244
|
T | C | 61 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(58): Show | 61 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1921-1033T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679244 | ||||||
| chr12:98679303
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1921-974A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679303 | ||||||
| chr12:98679396
|
G | A | 1 | a0001c0001t0004g0192 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1921-881G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679396 | ||||||
| chr12:98679465
|
C | T | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1921-812C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679465 | ||||||
| chr12:98679483
|
G | C | 1 | a0001c0001t0027g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1921-794G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679483 | ||||||
| chr12:98679571
|
C | T | 1 | a0001c0001t0011g0140 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1921-706C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679571 | ||||||
| chr12:98679650
|
T | A | 9 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0001g0231others(6): Show | 9 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1921-627T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679650 | ||||||
| chr12:98679717
|
C | T | 2 | a0001c0001t0007g0065a0001c0004t0007g0225 | 2 | HG03579.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1921-560C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679717 | ||||||
| chr12:98679768
|
A | G | 1 | a0001c0001t0001g0357 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1921-509A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679768 | ||||||
| chr12:98679811
|
C | T | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1921-466C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679811 | ||||||
| chr12:98679854
|
C | T | 61 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(58): Show | 61 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1921-423C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679854 | ||||||
| chr12:98679883
|
C | T | 2 | a0001c0001t0002g0329a0001c0001t0002g0347 | 2 | NA19057.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1921-394C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679883 | ||||||
| chr12:98679946
|
C | T | 1 | a0009c0007t0029g0304 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1921-331C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679946 | ||||||
| chr12:98679958
|
G | A | 1 | a0001c0001t0006g0166 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1921-319G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98679958 | ||||||
| chr12:98680039
|
C | T | 55 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(52): Show | 55 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1921-238C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98680039 | ||||||
| chr12:98680042
|
C | G | 1 | a0001c0001t0039g0008 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1921-235C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98680042 | ||||||
| chr12:98680094
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1921-183G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98680094 | ||||||
| chr12:98680252
|
A | C | 1 | a0001c0001t0012g0210 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1921-25A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 13/26 | chr12 | 98680252 | ||||||
| chr12:98680460
|
A | G | 1 | a0001c0001t0039g0008 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2046+58A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98680460 | ||||||
| chr12:98680758
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2046+356T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98680758 | ||||||
| chr12:98680770
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2046+368G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98680770 | ||||||
| chr12:98680975
|
A | G | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2046+573A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98680975 | ||||||
| chr12:98680994
|
G | A | 327 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(324): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.2046+592G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98680994 | ||||||
| chr12:98681017
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2046+615C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98681017 | ||||||
| chr12:98681021
|
A | G | 1 | a0001c0001t0003g0170 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2046+619A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98681021 | ||||||
| chr12:98681130
|
C | T | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2046+728C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98681130 | ||||||
| chr12:98681264
|
G | A | 1 | a0001c0001t0005g0060 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2046+862G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98681264 | ||||||
| chr12:98681392
|
C | T | 2 | a0001c0001t0015g0127a0001c0001t0015g0128 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2046+990C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98681392 | ||||||
| chr12:98681421
|
G | A | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2046+1019G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98681421 | ||||||
| chr12:98681423
|
G | A | 14 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(11): Show | 14 | HG02257.hp2 HG02647.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.2046+1021G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98681423 | ||||||
| chr12:98681969
|
A | G | 3 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303 | 3 | HG01884.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2047-1174A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98681969 | ||||||
| chr12:98682042
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2047-1101T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98682042 | ||||||
| chr12:98682044
|
A | AT | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2047-1092dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr12 | 98682044 | |||||
| chr12:98682052
|
G | GT | 40 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0030others(37): Show | 40 | HG00558.hp2 HG00642.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.2047-1072dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr12 | 98682052 | |||||
| chr12:98682052
|
G | T | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2047-1091G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98682052 | ||||||
| chr12:98682052
|
GT | G | 8 | a0001c0001t0001g0072a0001c0001t0001g0271a0001c0001t0003g0144others(5): Show | 8 | HG01496.hp2 HG01516.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2047-1072delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr12 | 98682052 | |||||
| chr12:98682060
|
T | G | 9 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0182others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2047-1083T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98682060 | ||||||
| chr12:98682198
|
C | T | 1 | a0001c0001t0002g0323 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2047-945C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98682198 | ||||||
| chr12:98682299
|
C | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0108others(3): Show | 6 | HG03098.hp2 HG03130.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2047-844C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98682299 | ||||||
| chr12:98682538
|
A | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0206others(36): Show | 40 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.2047-605A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98682538 | ||||||
| chr12:98682580
|
AT | A | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2047-555delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr12 | 98682580 | |||||
| chr12:98682729
|
T | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0206others(36): Show | 40 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.2047-414T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98682729 | ||||||
| chr12:98682760
|
G | A | 1 | a0001c0001t0037g0299 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2047-383G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98682760 | ||||||
| chr12:98682808
|
A | G | 361 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(358): Show | 364 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.2047-335A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98682808 | ||||||
| chr12:98682811
|
T | C | 6 | a0001c0001t0008g0308a0001c0001t0008g0310a0001c0001t0008g0311others(3): Show | 6 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2047-332T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98682811 | ||||||
| chr12:98682816
|
T | C | 7 | a0001c0001t0002g0221a0001c0001t0002g0315a0001c0001t0002g0316others(4): Show | 7 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2047-327T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98682816 | ||||||
| chr12:98682898
|
T | C | 1 | a0001c0001t0003g0149 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2047-245T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98682898 | ||||||
| chr12:98683077
|
C | G | 1 | a0001c0001t0003g0170 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2047-66C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98683077 | ||||||
| chr12:98683140
|
T | C | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.2047-3T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 14/26 | chr12 | 98683140 | ||||||
| chr12:98683348
|
G | T | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2178+74G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98683348 | ||||||
| chr12:98683379
|
T | A | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2178+105T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98683379 | ||||||
| chr12:98683801
|
T | C | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2178+527T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98683801 | ||||||
| chr12:98683965
|
T | G | 26 | a0001c0001t0001g0036a0001c0001t0001g0253a0001c0001t0001g0254others(23): Show | 26 | HG00140.hp1 HG00544.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.2178+691T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98683965 | ||||||
| chr12:98684008
|
A | G | 2 | a0001c0001t0008g0305a0001c0001t0008g0306 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2178+734A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98684008 | ||||||
| chr12:98684113
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2178+839A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98684113 | ||||||
| chr12:98684221
|
C | T | 6 | a0001c0001t0002g0333a0001c0001t0002g0339a0001c0001t0002g0349others(3): Show | 6 | HG00621.hp2 HG02970.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2178+947C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98684221 | ||||||
| chr12:98684222
|
G | A | 1 | a0001c0001t0006g0165 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2178+948G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98684222 | ||||||
| chr12:98684344
|
C | A | 1 | a0001c0001t0002g0325 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2178+1070C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98684344 | ||||||
| chr12:98684390
|
C | G | 6 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(3): Show | 6 | HG01081.hp1 HG01109.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.2178+1116C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98684390 | ||||||
| chr12:98684490
|
C | G | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.2178+1216C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98684490 | ||||||
| chr12:98684578
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2178+1304A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98684578 | ||||||
| chr12:98684744
|
A | C | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2178+1470A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98684744 | ||||||
| chr12:98684891
|
T | C | 6 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0361others(3): Show | 6 | HG01069.hp2 HG01515.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.2178+1617T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98684891 | ||||||
| chr12:98684959
|
C | T | 1 | a0001c0001t0015g0128 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2178+1685C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98684959 | ||||||
| chr12:98685081
|
A | G | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2179-1667A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98685081 | ||||||
| chr12:98685111
|
T | C | 64 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(61): Show | 64 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2179-1637T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98685111 | ||||||
| chr12:98685340
|
CT | C | 12 | a0001c0001t0001g0025a0001c0001t0001g0081a0001c0001t0003g0130others(9): Show | 12 | HG01081.hp1 HG01109.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.2179-1394delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr12 | 98685340 | |||||
| chr12:98685429
|
G | A | 8 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(5): Show | 8 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2179-1319G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98685429 | ||||||
| chr12:98685679
|
A | G | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2179-1069A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98685679 | ||||||
| chr12:98685862
|
C | G | 4 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0017g0202others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2179-886C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98685862 | ||||||
| chr12:98685880
|
G | A | 3 | a0001c0001t0010g0292a0001c0001t0010g0296a0001c0001t0010g0297 | 3 | NA18940.hp2 NA18952.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2179-868G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98685880 | ||||||
| chr12:98686172
|
T | G | 54 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(51): Show | 54 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.2179-576T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98686172 | ||||||
| chr12:98686265
|
A | C | 8 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(5): Show | 8 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2179-483A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98686265 | ||||||
| chr12:98686344
|
C | T | 1 | a0001c0001t0004g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2179-404C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98686344 | ||||||
| chr12:98686390
|
G | T | 5 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | HG01167.hp1 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2179-358G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98686390 | ||||||
| chr12:98686458
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2179-290A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98686458 | ||||||
| chr12:98686542
|
C | T | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.2179-206C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98686542 | ||||||
| chr12:98686721
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2179-27A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 15/26 | chr12 | 98686721 | ||||||
| chr12:98687090
|
T | C | 167 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(164): Show | 167 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.2304+217T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687090 | ||||||
| chr12:98687092
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2304+219C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687092 | ||||||
| chr12:98687192
|
G | A | 1 | a0001c0001t0016g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2304+319G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687192 | ||||||
| chr12:98687220
|
G | C | 1 | a0001c0001t0027g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2304+347G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687220 | ||||||
| chr12:98687260
|
G | A | 54 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(51): Show | 54 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.2304+387G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687260 | ||||||
| chr12:98687280
|
T | G | 1 | a0001c0001t0006g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2304+407T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687280 | ||||||
| chr12:98687285
|
C | T | 6 | a0001c0001t0036g0300a0001c0001t0037g0299a0001c0004t0007g0225others(3): Show | 6 | HG01081.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2304+412C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687285 | ||||||
| chr12:98687286
|
C | T | 1 | a0009c0007t0029g0304 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2304+413C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687286 | ||||||
| chr12:98687297
|
G | A | 54 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(51): Show | 54 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.2304+424G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687297 | ||||||
| chr12:98687357
|
G | A | 54 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(51): Show | 54 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.2304+484G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687357 | ||||||
| chr12:98687361
|
C | CA | 59 | a0001c0001t0001g0111a0001c0001t0001g0114a0001c0001t0002g0209others(56): Show | 59 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2304+504dupA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98687361 | |||||
| chr12:98687449
|
A | G | 1 | a0001c0001t0034g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2304+576A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687449 | ||||||
| chr12:98687498
|
T | A | 1 | a0001c0001t0001g0280 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2304+625T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687498 | ||||||
| chr12:98687583
|
CA | C | 8 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(5): Show | 8 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2304+711delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687583 | ||||||
| chr12:98687611
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0112 | 2 | HG00558.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2304+738G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687611 | ||||||
| chr12:98687699
|
G | C | 1 | a0001c0001t0004g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2304+826G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687699 | ||||||
| chr12:98687865
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0049others(1): Show | 4 | HG00621.hp1 HG02129.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.2304+992A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98687865 | ||||||
| chr12:98688135
|
T | C | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2304+1262T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98688135 | ||||||
| chr12:98688297
|
A | G | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2304+1424A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98688297 | ||||||
| chr12:98688404
|
G | A | 1 | a0001c0001t0002g0346 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2304+1531G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98688404 | ||||||
| chr12:98688470
|
CT | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.2304+1615delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98688470 | |||||
| chr12:98688470
|
CTT | C | 8 | a0001c0001t0002g0335a0001c0001t0003g0147a0001c0001t0012g0212others(5): Show | 8 | HG02451.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2304+1614_2304+161 others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98688470 | |||||
| chr12:98688530
|
G | C | 1 | a0001c0001t0001g0049 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2304+1657G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98688530 | ||||||
| chr12:98688638
|
A | AT | 14 | a0001c0001t0001g0278a0001c0001t0003g0158a0001c0001t0004g0198others(11): Show | 14 | HG00735.hp1 HG02155.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2304+1787dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98688638 | |||||
| chr12:98688638
|
AT | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(141): Show | 145 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.2304+1787delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98688638 | |||||
| chr12:98688638
|
ATT | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0057others(16): Show | 20 | HG00642.hp1 HG00733.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.2304+1786_2304+178 others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98688638 | |||||
| chr12:98688640
|
T | TTTC | 9 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(6): Show | 9 | HG01081.hp1 HG01109.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2304+1769_2304+177 others(7): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98688640 | |||||
| chr12:98688641
|
T | TTC | 50 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(47): Show | 50 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.2304+1769_2304+177 others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98688641 | |||||
| chr12:98688642
|
T | TC | 4 | a0001c0001t0002g0329a0001c0001t0002g0336a0001c0001t0002g0348others(1): Show | 4 | HG02698.hp1 NA18972.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.2304+1769_2304+177 others(5): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98688642 | ||||||
| chr12:98688668
|
G | A | 2 | a0002c0003t0007g0353a0002c0003t0007g0354 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2304+1795G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98688668 | ||||||
| chr12:98688717
|
A | T | 54 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(51): Show | 54 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.2304+1844A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98688717 | ||||||
| chr12:98688839
|
G | A | 4 | a0001c0001t0003g0141a0001c0001t0003g0146a0001c0001t0003g0147others(1): Show | 4 | NA18955.hp1 NA18986.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2304+1966G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98688839 | ||||||
| chr12:98688890
|
C | T | 2 | a0001c0001t0008g0305a0001c0001t0008g0306 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2304+2017C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98688890 | ||||||
| chr12:98688929
|
C | T | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2304+2056C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98688929 | ||||||
| chr12:98689075
|
G | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.2304+2202G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689075 | ||||||
| chr12:98689120
|
A | T | 11 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(8): Show | 11 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.2304+2247A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689120 | ||||||
| chr12:98689199
|
C | T | 7 | a0001c0001t0002g0221a0001c0001t0002g0315a0001c0001t0002g0316others(4): Show | 7 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2304+2326C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689199 | ||||||
| chr12:98689401
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2304+2528G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689401 | ||||||
| chr12:98689435
|
TGA | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(151): Show | 156 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.2304+2590_2304+259 others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98689435 | |||||
| chr12:98689435
|
TGAGA | T | 35 | a0001c0001t0001g0121a0001c0001t0002g0331a0001c0001t0002g0334others(32): Show | 35 | HG00140.hp2 HG00735.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.2304+2588_2304+259 others(8): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98689435 | |||||
| chr12:98689435
|
TGAGAGA | T | 57 | a0001c0001t0001g0004a0001c0001t0002g0209a0001c0001t0002g0221others(54): Show | 57 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.2304+2586_2304+259 others(10): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98689435 | |||||
| chr12:98689435
|
TGAGAGAG others(1): Show |
T | 71 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(68): Show | 71 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2304+2584_2304+259 others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98689435 | |||||
| chr12:98689435
|
TGAGAGAG others(3): Show |
T | 1 | a0001c0001t0003g0148 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2304+2582_2304+259 others(14): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98689435 | |||||
| chr12:98689435
|
TGAGAGAG others(7): Show |
T | 6 | a0001c0001t0036g0300a0001c0001t0037g0299a0001c0004t0007g0225others(3): Show | 6 | HG01081.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2304+2578_2304+259 others(18): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98689435 | |||||
| chr12:98689461
|
A | T | 3 | a0001c0001t0001g0121a0001c0001t0010g0295a0001c0001t0039g0008 | 3 | HG01346.hp2 NA18982.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2304+2588A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689461 | ||||||
| chr12:98689463
|
A | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0121others(4): Show | 7 | HG01346.hp2 HG02486.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2304+2590A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689463 | ||||||
| chr12:98689465
|
T | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0248 | 2 | NA18980.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2304+2592T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689465 | ||||||
| chr12:98689468
|
G | C | 1 | a0001c0001t0010g0295 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2304+2595G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689468 | ||||||
| chr12:98689470
|
G | C | 2 | a0001c0001t0001g0121a0001c0001t0039g0008 | 2 | HG01346.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2304+2597G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689470 | ||||||
| chr12:98689472
|
G | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0035 | 2 | HG02486.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.2304+2599G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689472 | ||||||
| chr12:98689474
|
C | CTGTG | 69 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.2304+2620_2304+262 others(8): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98689474 | |||||
| chr12:98689474
|
C | CTGTGTG | 13 | a0001c0001t0006g0164a0001c0001t0008g0305a0001c0001t0008g0306others(10): Show | 13 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.2304+2618_2304+262 others(10): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98689474 | |||||
| chr12:98689474
|
C | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0121others(2): Show | 5 | HG01346.hp2 HG02486.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.2304+2601C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689474 | ||||||
| chr12:98689495
|
T | A | 8 | a0001c0001t0001g0121a0001c0001t0001g0281a0001c0001t0001g0282others(5): Show | 8 | HG01346.hp2 NA18939.hp1 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2304+2622T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689495 | ||||||
| chr12:98689495
|
T | TGAGA | 4 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0017g0202others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2304+2629_2304+263 others(8): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98689495 | |||||
| chr12:98689495
|
T | TGTGA | 60 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(57): Show | 60 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.2304+2623_2304+262 others(8): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98689495 | |||||
| chr12:98689495
|
T | TGTGTGA | 16 | a0001c0001t0003g0139a0001c0001t0003g0154a0001c0001t0003g0167others(13): Show | 16 | HG02132.hp2 HG02451.hp1 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.2304+2623_2304+262 others(10): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98689495 | |||||
| chr12:98689495
|
T | TGTGTGAG others(1): Show |
3 | a0001c0001t0012g0212a0001c0001t0033g0213a0008c0009t0012g0211 | 3 | HG02647.hp2 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2304+2623_2304+262 others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98689495 | |||||
| chr12:98689497
|
A | T | 54 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(51): Show | 54 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.2304+2624A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689497 | ||||||
| chr12:98689533
|
C | T | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2304+2660C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689533 | ||||||
| chr12:98689928
|
A | G | 10 | a0001c0001t0001g0206a0001c0001t0001g0228a0001c0001t0001g0230others(7): Show | 10 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.2304+3055A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98689928 | ||||||
| chr12:98690021
|
A | T | 64 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(61): Show | 64 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2304+3148A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98690021 | ||||||
| chr12:98690177
|
A | G | 2 | a0002c0003t0007g0353a0002c0003t0007g0354 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2304+3304A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98690177 | ||||||
| chr12:98690548
|
A | G | 330 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(327): Show | 332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.2304+3675A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98690548 | ||||||
| chr12:98690596
|
G | A | 1 | a0001c0001t0001g0363 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2304+3723G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98690596 | ||||||
| chr12:98690609
|
C | A | 22 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0257others(19): Show | 22 | HG00140.hp1 HG00544.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.2304+3736C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98690609 | ||||||
| chr12:98690658
|
G | T | 1 | a0001c0001t0001g0261 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2304+3785G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98690658 | ||||||
| chr12:98690806
|
C | T | 6 | a0001c0001t0036g0300a0001c0001t0037g0299a0001c0004t0007g0225others(3): Show | 6 | HG01081.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2304+3933C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98690806 | ||||||
| chr12:98690838
|
G | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0108others(2): Show | 5 | HG03098.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2304+3965G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98690838 | ||||||
| chr12:98691248
|
C | A | 73 | a0001c0001t0001g0121a0001c0001t0003g0125a0001c0001t0003g0130others(70): Show | 73 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2304+4375C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98691248 | ||||||
| chr12:98691249
|
C | A | 73 | a0001c0001t0001g0121a0001c0001t0003g0125a0001c0001t0003g0130others(70): Show | 73 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2304+4376C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98691249 | ||||||
| chr12:98691369
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2304+4496G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98691369 | ||||||
| chr12:98691383
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2304+4510C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98691383 | ||||||
| chr12:98691730
|
G | A | 13 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(10): Show | 13 | HG02647.hp2 HG02717.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.2304+4857G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98691730 | ||||||
| chr12:98691931
|
T | C | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2304+5058T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98691931 | ||||||
| chr12:98692011
|
ACCATG | A | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2304+5141_2304+514 others(9): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98692011 | |||||
| chr12:98692086
|
C | A | 1 | a0001c0001t0036g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2304+5213C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98692086 | ||||||
| chr12:98692143
|
C | T | 4 | a0001c0001t0008g0308a0001c0001t0008g0311a0001c0001t0008g0312others(1): Show | 4 | HG00735.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2304+5270C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98692143 | ||||||
| chr12:98692157
|
A | ACTGCAAG others(10): Show |
2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2304+5285_2304+530 others(21): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98692157 | |||||
| chr12:98692244
|
G | C | 1 | a0001c0001t0003g0133 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2304+5371G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98692244 | ||||||
| chr12:98692334
|
C | T | 4 | a0001c0001t0012g0212a0001c0001t0012g0218a0001c0001t0033g0213others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2304+5461C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98692334 | ||||||
| chr12:98692374
|
C | T | 4 | a0001c0001t0012g0212a0001c0001t0012g0218a0001c0001t0033g0213others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2304+5501C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98692374 | ||||||
| chr12:98692430
|
A | C | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2304+5557A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98692430 | ||||||
| chr12:98692609
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2304+5736A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98692609 | ||||||
| chr12:98692645
|
A | G | 24 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(21): Show | 24 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.2304+5772A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98692645 | ||||||
| chr12:98692727
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2304+5854A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98692727 | ||||||
| chr12:98692819
|
T | C | 5 | a0001c0001t0002g0221a0001c0001t0002g0316a0001c0001t0002g0317others(2): Show | 5 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2304+5946T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98692819 | ||||||
| chr12:98692857
|
G | T | 1 | a0001c0001t0021g0321 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2304+5984G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98692857 | ||||||
| chr12:98693000
|
C | T | 1 | a0001c0001t0028g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2304+6127C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693000 | ||||||
| chr12:98693065
|
TAA | T | 63 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2304+6203_2304+620 others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98693065 | |||||
| chr12:98693070
|
A | C | 1 | a0001c0001t0004g0200 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2304+6197A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693070 | ||||||
| chr12:98693075
|
A | C | 5 | a0001c0002t0001g0355a0001c0002t0023g0309a0001c0002t0032g0217others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2304+6202A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693075 | ||||||
| chr12:98693142
|
T | C | 1 | a0008c0009t0012g0211 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2305-6266T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693142 | ||||||
| chr12:98693497
|
A | G | 1 | a0001c0001t0002g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2305-5911A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693497 | ||||||
| chr12:98693557
|
A | G | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2305-5851A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693557 | ||||||
| chr12:98693589
|
T | A | 1 | a0001c0001t0012g0210 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2305-5819T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693589 | ||||||
| chr12:98693616
|
A | C | 1 | a0001c0001t0001g0264 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2305-5792A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693616 | ||||||
| chr12:98693683
|
G | A | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2305-5725G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693683 | ||||||
| chr12:98693753
|
C | T | 5 | a0001c0001t0003g0139a0001c0001t0003g0154a0001c0001t0003g0167others(2): Show | 5 | HG02132.hp2 NA18945.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.2305-5655C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693753 | ||||||
| chr12:98693777
|
A | G | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2305-5631A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693777 | ||||||
| chr12:98693792
|
G | GT | 53 | a0001c0001t0001g0031a0001c0001t0001g0074a0001c0001t0001g0287others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2305-5600dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98693792 | |||||
| chr12:98693792
|
GT | G | 22 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0118others(19): Show | 22 | HG00639.hp2 HG00735.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.2305-5600delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98693792 | |||||
| chr12:98693809
|
C | T | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2305-5599C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693809 | ||||||
| chr12:98693810
|
G | A | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2305-5598G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693810 | ||||||
| chr12:98693832
|
T | C | 63 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2305-5576T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693832 | ||||||
| chr12:98693898
|
T | G | 2 | a0001c0001t0001g0041a0001c0001t0007g0065 | 2 | HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2305-5510T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98693898 | ||||||
| chr12:98694066
|
G | A | 1 | a0001c0001t0016g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2305-5342G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98694066 | ||||||
| chr12:98694152
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2305-5256A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98694152 | ||||||
| chr12:98694250
|
C | T | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2305-5158C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98694250 | ||||||
| chr12:98694316
|
A | G | 97 | a0001c0001t0001g0121a0001c0001t0003g0125a0001c0001t0003g0130others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.2305-5092A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98694316 | ||||||
| chr12:98694445
|
A | T | 73 | a0001c0001t0001g0121a0001c0001t0003g0125a0001c0001t0003g0130others(70): Show | 73 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2305-4963A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98694445 | ||||||
| chr12:98694703
|
T | A | 1 | a0001c0001t0015g0128 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2305-4705T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98694703 | ||||||
| chr12:98694839
|
G | T | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2305-4569G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98694839 | ||||||
| chr12:98694848
|
C | T | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2305-4560C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98694848 | ||||||
| chr12:98694877
|
A | AT | 29 | a0001c0001t0001g0025a0001c0001t0002g0333a0001c0001t0002g0339others(26): Show | 29 | HG00140.hp2 HG00621.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.2305-4513dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98694877 | |||||
| chr12:98694943
|
C | T | 1 | a0001c0001t0003g0158 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2305-4465C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98694943 | ||||||
| chr12:98694970
|
G | A | 1 | a0001c0001t0004g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2305-4438G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98694970 | ||||||
| chr12:98694984
|
T | G | 2 | a0001c0001t0003g0144a0001c0001t0003g0145 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2305-4424T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98694984 | ||||||
| chr12:98695035
|
C | T | 1 | a0001c0001t0003g0224 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2305-4373C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695035 | ||||||
| chr12:98695087
|
C | G | 57 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(54): Show | 57 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2305-4321C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695087 | ||||||
| chr12:98695089
|
G | A | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2305-4319G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695089 | ||||||
| chr12:98695148
|
G | A | 3 | a0001c0001t0039g0008a0001c0004t0007g0225a0001c0004t0007g0226 | 3 | HG02258.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2305-4260G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695148 | ||||||
| chr12:98695353
|
G | GC | 61 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0093others(58): Show | 61 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.2305-4046dupC | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98695353 | |||||
| chr12:98695362
|
C | T | 2 | a0001c0001t0013g0302a0001c0001t0013g0303 | 2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2305-4046C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695362 | ||||||
| chr12:98695363
|
T | C | 4 | a0001c0001t0001g0260a0001c0001t0002g0221a0001c0001t0002g0338others(1): Show | 4 | HG01192.hp1 HG02735.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2305-4045T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695363 | ||||||
| chr12:98695381
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2305-4027G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695381 | ||||||
| chr12:98695388
|
ACT | A | 3 | a0001c0002t0001g0355a0002c0003t0007g0353a0002c0003t0007g0354 | 3 | HG02280.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2305-4017_2305-401 others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr12 | 98695388 | |||||
| chr12:98695403
|
C | G | 1 | a0001c0001t0003g0158 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2305-4005C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695403 | ||||||
| chr12:98695543
|
A | G | 2 | a0001c0001t0001g0261a0001c0001t0001g0272 | 2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2305-3865A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695543 | ||||||
| chr12:98695545
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0288 | 2 | HG00140.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.2305-3863C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695545 | ||||||
| chr12:98695707
|
C | T | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2305-3701C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695707 | ||||||
| chr12:98695774
|
T | G | 1 | a0001c0001t0001g0011 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2305-3634T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695774 | ||||||
| chr12:98695817
|
T | G | 1 | a0002c0003t0007g0353 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2305-3591T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695817 | ||||||
| chr12:98695875
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2305-3533T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695875 | ||||||
| chr12:98695881
|
G | A | 2 | a0001c0001t0009g0084a0001c0001t0009g0255 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2305-3527G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695881 | ||||||
| chr12:98695957
|
T | C | 4 | a0001c0001t0001g0277a0001c0001t0005g0066a0001c0001t0005g0076others(1): Show | 4 | NA18962.hp1 NA18994.hp1 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.2305-3451T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98695957 | ||||||
| chr12:98696352
|
C | A | 14 | a0001c0001t0004g0178a0001c0001t0004g0179a0001c0001t0004g0180others(11): Show | 14 | HG00280.hp2 HG00738.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.2305-3056C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98696352 | ||||||
| chr12:98696383
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2305-3025C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98696383 | ||||||
| chr12:98696636
|
C | A | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2305-2772C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98696636 | ||||||
| chr12:98696652
|
G | C | 1 | a0001c0001t0001g0359 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2305-2756G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98696652 | ||||||
| chr12:98696655
|
C | G | 2 | a0001c0002t0023g0309a0001c0002t0032g0217 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2305-2753C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98696655 | ||||||
| chr12:98696795
|
C | G | 8 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(5): Show | 8 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2305-2613C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98696795 | ||||||
| chr12:98696895
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0108others(2): Show | 5 | HG03098.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2305-2513A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98696895 | ||||||
| chr12:98696926
|
C | A | 1 | a0001c0001t0001g0266 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2305-2482C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98696926 | ||||||
| chr12:98697064
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2305-2344G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98697064 | ||||||
| chr12:98697221
|
GTGAGGTG others(1): Show |
G | 14 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(11): Show | 14 | HG02257.hp2 HG02647.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.2305-2186_2305-217 others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98697221 | ||||||
| chr12:98697417
|
G | A | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2305-1991G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98697417 | ||||||
| chr12:98697561
|
C | T | 62 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(59): Show | 62 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2305-1847C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98697561 | ||||||
| chr12:98697963
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0108others(2): Show | 5 | HG03098.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2305-1445C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98697963 | ||||||
| chr12:98698200
|
T | A | 9 | a0001c0001t0003g0130a0001c0001t0003g0131a0001c0001t0003g0133others(6): Show | 9 | HG02970.hp2 HG03516.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.2305-1208T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98698200 | ||||||
| chr12:98698508
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2305-900G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98698508 | ||||||
| chr12:98698578
|
C | T | 3 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303 | 3 | HG01884.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2305-830C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98698578 | ||||||
| chr12:98698634
|
C | A | 2 | a0004c0006t0001g0256a0004c0006t0001g0356 | 2 | NA18946.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2305-774C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98698634 | ||||||
| chr12:98698824
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2305-584A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98698824 | ||||||
| chr12:98698843
|
A | G | 63 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2305-565A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98698843 | ||||||
| chr12:98698961
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2305-447G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98698961 | ||||||
| chr12:98699059
|
A | G | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2305-349A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98699059 | ||||||
| chr12:98699205
|
G | A | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2305-203G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98699205 | ||||||
| chr12:98699232
|
C | T | 1 | a0001c0001t0003g0133 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2305-176C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98699232 | ||||||
| chr12:98699235
|
A | G | 7 | a0001c0001t0002g0221a0001c0001t0002g0315a0001c0001t0002g0316others(4): Show | 7 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2305-173A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 16/26 | chr12 | 98699235 | ||||||
| chr12:98699590
|
A | T | 1 | a0001c0001t0001g0004 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2466+21A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98699590 | ||||||
| chr12:98699718
|
C | A | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2466+149C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98699718 | ||||||
| chr12:98699786
|
G | A | 2 | a0001c0001t0006g0150a0001c0001t0006g0164 | 2 | NA18979.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2466+217G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98699786 | ||||||
| chr12:98699796
|
G | A | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2466+227G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98699796 | ||||||
| chr12:98700202
|
C | T | 1 | a0009c0007t0029g0304 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2466+633C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98700202 | ||||||
| chr12:98700255
|
A | G | 2 | a0001c0001t0018g0009a0001c0001t0018g0010 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2466+686A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98700255 | ||||||
| chr12:98700328
|
T | G | 9 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0038others(6): Show | 9 | HG01099.hp2 HG01358.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.2466+759T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98700328 | ||||||
| chr12:98700367
|
C | T | 5 | a0001c0001t0001g0240a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG02132.hp1 HG02155.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.2466+798C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98700367 | ||||||
| chr12:98700621
|
A | G | 2 | a0001c0001t0001g0267a0001c0001t0001g0273 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.2466+1052A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98700621 | ||||||
| chr12:98700649
|
C | G | 1 | a0001c0001t0001g0270 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2466+1080C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98700649 | ||||||
| chr12:98700706
|
A | G | 45 | a0001c0001t0002g0209a0001c0001t0002g0314a0001c0001t0002g0324others(42): Show | 45 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2466+1137A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98700706 | ||||||
| chr12:98700715
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2466+1146C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98700715 | ||||||
| chr12:98700943
|
C | T | 6 | a0001c0001t0036g0300a0001c0001t0037g0299a0001c0004t0007g0225others(3): Show | 6 | HG01081.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2466+1374C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98700943 | ||||||
| chr12:98701004
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(152): Show | 157 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.2466+1435T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98701004 | ||||||
| chr12:98701159
|
G | A | 4 | a0001c0001t0036g0300a0001c0001t0037g0299a0003c0005t0007g0219others(1): Show | 4 | HG01081.hp1 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2466+1590G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98701159 | ||||||
| chr12:98701341
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2466+1772T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98701341 | ||||||
| chr12:98701362
|
A | G | 1 | a0001c0001t0036g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2466+1793A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98701362 | ||||||
| chr12:98701397
|
A | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2466+1828A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98701397 | ||||||
| chr12:98701406
|
G | T | 2 | a0001c0002t0023g0309a0001c0002t0032g0217 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2466+1837G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98701406 | ||||||
| chr12:98701599
|
G | A | 1 | a0001c0001t0038g0320 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2467-1772G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98701599 | ||||||
| chr12:98701670
|
A | G | 38 | a0001c0001t0001g0121a0001c0001t0003g0125a0001c0001t0003g0130others(35): Show | 38 | HG00408.hp2 HG00558.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.2467-1701A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98701670 | ||||||
| chr12:98701701
|
T | C | 24 | a0001c0001t0002g0314a0001c0001t0002g0326a0001c0001t0002g0327others(21): Show | 24 | HG00323.hp2 HG01257.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.2467-1670T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98701701 | ||||||
| chr12:98701746
|
G | T | 1 | a0001c0001t0004g0191 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2467-1625G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98701746 | ||||||
| chr12:98701827
|
T | C | 1 | a0001c0001t0004g0188 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2467-1544T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98701827 | ||||||
| chr12:98702084
|
G | A | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0288 | 3 | HG00140.hp1 HG01361.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2467-1287G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98702084 | ||||||
| chr12:98702113
|
T | C | 328 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.2467-1258T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98702113 | ||||||
| chr12:98702191
|
G | A | 52 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(49): Show | 52 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.2467-1180G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98702191 | ||||||
| chr12:98702236
|
T | C | 38 | a0001c0001t0001g0121a0001c0001t0003g0125a0001c0001t0003g0130others(35): Show | 38 | HG00408.hp2 HG00558.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.2467-1135T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98702236 | ||||||
| chr12:98702328
|
G | A | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2467-1043G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98702328 | ||||||
| chr12:98702429
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(86): Show | 90 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.2467-942T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98702429 | ||||||
| chr12:98702570
|
A | G | 3 | a0001c0001t0012g0212a0001c0001t0033g0213a0008c0009t0012g0211 | 3 | HG02647.hp2 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2467-801A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98702570 | ||||||
| chr12:98702599
|
C | T | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2467-772C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98702599 | ||||||
| chr12:98702619
|
G | T | 1 | a0001c0001t0024g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2467-752G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98702619 | ||||||
| chr12:98702680
|
C | G | 6 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(3): Show | 6 | HG04228.hp1 NA18940.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.2467-691C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98702680 | ||||||
| chr12:98702841
|
C | CA | 51 | a0001c0001t0001g0121a0001c0001t0001g0253a0001c0001t0001g0290others(48): Show | 51 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.2467-512dupA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr12 | 98702841 | |||||
| chr12:98702841
|
C | CAAA | 12 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(9): Show | 12 | HG02647.hp2 HG02717.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.2467-514_2467-512d others(5): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr12 | 98702841 | |||||
| chr12:98702841
|
CA | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0246others(5): Show | 8 | HG01109.hp1 HG01169.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.2467-512delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr12 | 98702841 | |||||
| chr12:98702942
|
G | T | 6 | a0001c0001t0036g0300a0001c0001t0037g0299a0001c0004t0007g0225others(3): Show | 6 | HG01081.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2467-429G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98702942 | ||||||
| chr12:98703179
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2467-192G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98703179 | ||||||
| chr12:98703299
|
A | T | 4 | a0001c0001t0003g0141a0001c0001t0003g0146a0001c0001t0003g0147others(1): Show | 4 | NA18955.hp1 NA18986.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2467-72A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 17/26 | chr12 | 98703299 | ||||||
| chr12:98703692
|
G | A | 327 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(324): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.2595+193G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98703692 | ||||||
| chr12:98703890
|
T | C | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2595+391T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98703890 | ||||||
| chr12:98703892
|
C | T | 4 | a0001c0001t0036g0300a0001c0001t0037g0299a0003c0005t0007g0219others(1): Show | 4 | HG01081.hp1 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2595+393C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98703892 | ||||||
| chr12:98703942
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2595+443C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98703942 | ||||||
| chr12:98704023
|
T | A | 24 | a0001c0001t0002g0314a0001c0001t0002g0326a0001c0001t0002g0327others(21): Show | 24 | HG00323.hp2 HG01257.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.2595+524T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98704023 | ||||||
| chr12:98704066
|
C | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0108others(2): Show | 5 | HG03098.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2595+567C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98704066 | ||||||
| chr12:98704125
|
C | CT | 6 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0043others(3): Show | 6 | HG03098.hp2 HG03130.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2595+637dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr12 | 98704125 | |||||
| chr12:98704133
|
T | G | 73 | a0001c0001t0001g0121a0001c0001t0003g0125a0001c0001t0003g0130others(70): Show | 73 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2595+634T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98704133 | ||||||
| chr12:98704152
|
T | TG | 52 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(49): Show | 52 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.2595+658dupG | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr12 | 98704152 | |||||
| chr12:98704157
|
G | T | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2595+658G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98704157 | ||||||
| chr12:98704212
|
C | A | 1 | a0001c0001t0001g0232 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2595+713C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98704212 | ||||||
| chr12:98704283
|
T | C | 5 | a0001c0002t0001g0355a0001c0002t0023g0309a0001c0002t0032g0217others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2595+784T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98704283 | ||||||
| chr12:98704446
|
C | T | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2595+947C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98704446 | ||||||
| chr12:98704586
|
T | C | 3 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303 | 3 | HG01884.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2595+1087T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98704586 | ||||||
| chr12:98704677
|
G | A | 1 | a0009c0007t0029g0304 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2595+1178G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98704677 | ||||||
| chr12:98704749
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2595+1250G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98704749 | ||||||
| chr12:98704768
|
A | G | 1 | a0001c0001t0020g0352 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2595+1269A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98704768 | ||||||
| chr12:98704770
|
G | C | 6 | a0001c0001t0036g0300a0001c0001t0037g0299a0001c0004t0007g0225others(3): Show | 6 | HG01081.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2595+1271G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98704770 | ||||||
| chr12:98705146
|
C | G | 37 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(34): Show | 37 | HG00408.hp2 HG00558.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.2596-1339C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98705146 | ||||||
| chr12:98705191
|
A | G | 1 | a0001c0001t0005g0082 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2596-1294A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98705191 | ||||||
| chr12:98705343
|
G | T | 1 | a0001c0001t0003g0156 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2596-1142G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98705343 | ||||||
| chr12:98705675
|
G | T | 1 | a0001c0001t0002g0341 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2596-810G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98705675 | ||||||
| chr12:98705788
|
A | G | 4 | a0001c0001t0002g0333a0001c0001t0002g0339a0001c0001t0002g0349others(1): Show | 4 | HG00621.hp2 NA18948.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.2596-697A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98705788 | ||||||
| chr12:98705803
|
A | G | 1 | a0001c0001t0027g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2596-682A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98705803 | ||||||
| chr12:98706406
|
T | C | 2 | a0002c0003t0007g0353a0002c0003t0007g0354 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2596-79T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 18/26 | chr12 | 98706406 | ||||||
| chr12:98706665
|
C | T | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2721+55C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98706665 | ||||||
| chr12:98706709
|
TA | T | 24 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(21): Show | 24 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.2721+100delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98706709 | ||||||
| chr12:98706938
|
A | T | 2 | a0001c0001t0015g0127a0001c0001t0015g0128 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2721+328A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98706938 | ||||||
| chr12:98707329
|
G | C | 2 | a0001c0002t0023g0309a0001c0002t0032g0217 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2721+719G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98707329 | ||||||
| chr12:98707362
|
A | C | 1 | a0001c0001t0007g0065 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2721+752A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98707362 | ||||||
| chr12:98707457
|
A | G | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG00140.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2721+847A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98707457 | ||||||
| chr12:98707531
|
A | G | 1 | a0001c0001t0014g0293 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2721+921A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98707531 | ||||||
| chr12:98707632
|
G | A | 168 | a0001c0001t0001g0121a0001c0001t0002g0209a0001c0001t0002g0221others(165): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.2722-953G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98707632 | ||||||
| chr12:98707663
|
T | C | 97 | a0001c0001t0001g0121a0001c0001t0003g0125a0001c0001t0003g0130others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.2722-922T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98707663 | ||||||
| chr12:98707679
|
A | G | 63 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2722-906A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98707679 | ||||||
| chr12:98707692
|
C | CTA | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(137): Show | 142 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.2722-874_2722-873d others(4): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707692 | |||||
| chr12:98707692
|
C | CTATA | 18 | a0001c0001t0001g0011a0001c0001t0001g0102a0001c0001t0001g0113others(15): Show | 18 | HG02129.hp1 HG02258.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.2722-876_2722-873d others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707692 | |||||
| chr12:98707692
|
C | CTATATA | 5 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(2): Show | 5 | HG01081.hp1 HG01109.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.2722-878_2722-873d others(8): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707692 | |||||
| chr12:98707692
|
C | CTATATAT others(5): Show |
1 | a0001c0001t0038g0320 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2722-884_2722-873d others(14): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707692 | |||||
| chr12:98707692
|
C | CTATATAT others(9): Show |
5 | a0001c0001t0002g0314a0001c0001t0002g0323a0001c0001t0002g0336others(2): Show | 5 | HG04228.hp2 NA18747.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2722-888_2722-873d others(18): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707692 | |||||
| chr12:98707692
|
C | CTATATAT others(11): Show |
29 | a0001c0001t0002g0209a0001c0001t0002g0324a0001c0001t0002g0326others(26): Show | 29 | HG00408.hp1 HG01257.hp1 HG01952.hp1 others(26): Show |
intron_variant | MODIFIER | c.2722-890_2722-873d others(20): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707692 | |||||
| chr12:98707692
|
C | CTATATAT others(13): Show |
4 | a0001c0001t0002g0325a0001c0001t0002g0333a0001c0001t0006g0166others(1): Show | 4 | HG00323.hp2 HG02148.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.2722-892_2722-873d others(22): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707692 | |||||
| chr12:98707692
|
C | CTATATAT others(15): Show |
5 | a0001c0001t0002g0338a0001c0001t0002g0339a0001c0001t0002g0349others(2): Show | 5 | HG00621.hp2 HG02273.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.2722-873_2722-872i others(24): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707692 | |||||
| chr12:98707692
|
C | CTATATAT others(17): Show |
1 | a0001c0001t0002g0315 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2722-873_2722-872i others(26): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707692 | |||||
| chr12:98707692
|
C | CTATATAT others(19): Show |
1 | a0001c0001t0002g0221 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2722-873_2722-872i others(28): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707692 | |||||
| chr12:98707692
|
C | CTATATAT others(23): Show |
2 | a0001c0001t0002g0316a0001c0001t0002g0317 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2722-873_2722-872i others(32): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707692 | |||||
| chr12:98707692
|
C | CTATATAT others(25): Show |
2 | a0001c0001t0002g0319a0001c0001t0007g0250 | 2 | HG00642.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.2722-873_2722-872i others(34): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707692 | |||||
| chr12:98707709
|
T | TATATATA others(17): Show |
1 | a0001c0001t0002g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2722-873_2722-872i others(26): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707709 | |||||
| chr12:98707711
|
T | C | 1 | a0001c0001t0002g0346 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2722-874T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98707711 | ||||||
| chr12:98707711
|
T | TATATATA others(11): Show |
1 | a0001c0001t0006g0165 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2722-873_2722-872i others(20): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707711 | |||||
| chr12:98707711
|
T | TATATATA others(13): Show |
1 | a0001c0001t0002g0342 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2722-873_2722-872i others(22): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 98707711 | |||||
| chr12:98707806
|
A | G | 3 | a0001c0001t0015g0127a0001c0001t0015g0128a0001c0001t0030g0007 | 3 | HG01891.hp2 HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2722-779A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98707806 | ||||||
| chr12:98707910
|
G | A | 1 | a0009c0007t0029g0304 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2722-675G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98707910 | ||||||
| chr12:98707969
|
C | T | 12 | a0001c0001t0001g0003a0001c0001t0001g0228a0001c0001t0001g0230others(9): Show | 13 | HG00642.hp1 HG00733.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.2722-616C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98707969 | ||||||
| chr12:98708192
|
G | A | 5 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0168others(2): Show | 5 | HG00408.hp2 HG00558.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.2722-393G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98708192 | ||||||
| chr12:98708204
|
C | T | 4 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0271others(1): Show | 4 | HG00741.hp1 HG01192.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2722-381C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98708204 | ||||||
| chr12:98708223
|
G | A | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2722-362G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98708223 | ||||||
| chr12:98708237
|
G | A | 1 | a0001c0001t0034g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2722-348G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98708237 | ||||||
| chr12:98708245
|
C | A | 1 | a0001c0001t0004g0205 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2722-340C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98708245 | ||||||
| chr12:98708259
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2722-326T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98708259 | ||||||
| chr12:98708321
|
G | C | 1 | a0001c0002t0023g0309 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2722-264G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 19/26 | chr12 | 98708321 | ||||||
| chr12:98709090
|
A | C | 1 | a0001c0001t0036g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2841+386A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98709090 | ||||||
| chr12:98709272
|
T | C | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2841+568T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98709272 | ||||||
| chr12:98709397
|
A | G | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2841+693A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98709397 | ||||||
| chr12:98709467
|
G | A | 7 | a0001c0001t0002g0221a0001c0001t0002g0315a0001c0001t0002g0316others(4): Show | 7 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2841+763G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98709467 | ||||||
| chr12:98709474
|
G | A | 8 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(5): Show | 8 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2841+770G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98709474 | ||||||
| chr12:98709532
|
T | C | 8 | a0001c0001t0002g0221a0001c0001t0002g0315a0001c0001t0002g0316others(5): Show | 8 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2841+828T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98709532 | ||||||
| chr12:98709542
|
G | A | 8 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(5): Show | 8 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2841+838G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98709542 | ||||||
| chr12:98709579
|
C | T | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2841+875C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98709579 | ||||||
| chr12:98709998
|
C | T | 37 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(34): Show | 37 | HG00408.hp2 HG00558.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.2841+1294C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98709998 | ||||||
| chr12:98710163
|
C | T | 9 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0001g0231others(6): Show | 9 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2841+1459C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98710163 | ||||||
| chr12:98710179
|
G | GT | 31 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0056others(28): Show | 31 | HG00438.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2841+1494dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr12 | 98710179 | |||||
| chr12:98710179
|
G | GTT | 66 | a0001c0001t0003g0130a0001c0001t0003g0131a0001c0001t0003g0133others(63): Show | 66 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.2841+1493_2841+149 others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr12 | 98710179 | |||||
| chr12:98710179
|
G | GTTT | 14 | a0001c0001t0001g0284a0001c0001t0003g0125a0001c0001t0003g0139others(11): Show | 14 | HG01258.hp2 HG01358.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2841+1492_2841+149 others(7): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr12 | 98710179 | |||||
| chr12:98710179
|
GT | G | 53 | a0001c0001t0002g0209a0001c0001t0002g0314a0001c0001t0002g0315others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.2841+1494delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr12 | 98710179 | |||||
| chr12:98710187
|
T | G | 1 | a0001c0001t0001g0049 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2841+1483T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98710187 | ||||||
| chr12:98710270
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2841+1566G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98710270 | ||||||
| chr12:98710503
|
G | A | 4 | a0001c0001t0015g0127a0001c0001t0015g0128a0001c0001t0015g0129others(1): Show | 4 | HG01891.hp2 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2841+1799G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98710503 | ||||||
| chr12:98710643
|
T | C | 159 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(156): Show | 159 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.2842-1676T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98710643 | ||||||
| chr12:98710727
|
A | C | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2842-1592A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98710727 | ||||||
| chr12:98710767
|
A | G | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2842-1552A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98710767 | ||||||
| chr12:98710844
|
T | C | 1 | a0001c0001t0013g0303 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2842-1475T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98710844 | ||||||
| chr12:98710881
|
TA | T | 63 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2842-1435delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr12 | 98710881 | |||||
| chr12:98711118
|
A | C | 1 | a0001c0001t0001g0269 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2842-1201A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98711118 | ||||||
| chr12:98711446
|
G | C | 28 | a0001c0001t0001g0061a0001c0001t0001g0277a0001c0001t0005g0040others(25): Show | 28 | HG02080.hp1 HG02135.hp1 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.2842-873G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98711446 | ||||||
| chr12:98711813
|
C | G | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2842-506C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98711813 | ||||||
| chr12:98711835
|
A | AAAGAATC others(137): Show |
1 | a0001c0001t0001g0263 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2842-475_2842-474i others(146): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr12 | 98711835 | |||||
| chr12:98711857
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02055.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2842-462T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98711857 | ||||||
| chr12:98711951
|
A | G | 1 | a0001c0001t0003g0167 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2842-368A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98711951 | ||||||
| chr12:98712015
|
C | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(152): Show | 157 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.2842-304C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98712015 | ||||||
| chr12:98712061
|
C | T | 1 | a0001c0001t0004g0195 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2842-258C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98712061 | ||||||
| chr12:98712062
|
G | A | 1 | a0001c0001t0004g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2842-257G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 20/26 | chr12 | 98712062 | ||||||
| chr12:98712504
|
G | T | 1 | a0001c0001t0002g0221 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2958+69G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98712504 | ||||||
| chr12:98712562
|
C | T | 54 | a0001c0001t0001g0363a0001c0001t0002g0209a0001c0001t0002g0221others(51): Show | 54 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2958+127C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98712562 | ||||||
| chr12:98712589
|
C | T | 167 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(164): Show | 167 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.2958+154C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98712589 | ||||||
| chr12:98712664
|
A | G | 167 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(164): Show | 167 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.2958+229A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98712664 | ||||||
| chr12:98712709
|
C | A | 1 | a0001c0001t0005g0115 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2958+274C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98712709 | ||||||
| chr12:98712786
|
T | C | 2 | a0002c0003t0007g0353a0002c0003t0007g0354 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2958+351T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98712786 | ||||||
| chr12:98712825
|
C | CT | 52 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(49): Show | 52 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.2958+400dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98712825 | |||||
| chr12:98712882
|
A | G | 1 | a0001c0001t0006g0223 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2958+447A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98712882 | ||||||
| chr12:98713216
|
A | G | 1 | a0001c0001t0002g0209 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2958+781A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98713216 | ||||||
| chr12:98713306
|
A | C | 1 | a0001c0001t0001g0271 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2958+871A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98713306 | ||||||
| chr12:98713385
|
A | G | 3 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | HG02723.hp1 HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2958+950A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98713385 | ||||||
| chr12:98713685
|
C | T | 8 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(5): Show | 8 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2958+1250C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98713685 | ||||||
| chr12:98713730
|
A | G | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2958+1295A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98713730 | ||||||
| chr12:98713743
|
T | A | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2958+1308T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98713743 | ||||||
| chr12:98713846
|
T | C | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2958+1411T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98713846 | ||||||
| chr12:98713953
|
T | C | 3 | a0001c0001t0004g0180a0001c0001t0004g0181a0001c0001t0004g0189 | 3 | HG01258.hp2 HG01358.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2959-1474T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98713953 | ||||||
| chr12:98714321
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2959-1106A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98714321 | ||||||
| chr12:98714510
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(151): Show | 156 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.2959-917A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98714510 | ||||||
| chr12:98714578
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2959-849T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98714578 | ||||||
| chr12:98714581
|
T | G | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2959-846T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98714581 | ||||||
| chr12:98714733
|
C | A | 1 | a0001c0001t0001g0261 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2959-694C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98714733 | ||||||
| chr12:98714833
|
CT | C | 14 | a0001c0001t0004g0178a0001c0001t0004g0179a0001c0001t0004g0180others(11): Show | 14 | HG00280.hp2 HG00738.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.2959-585delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98714833 | |||||
| chr12:98715073
|
C | CT | 52 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0032others(49): Show | 53 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.2959-339dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715073 | |||||
| chr12:98715128
|
G | C | 2 | a0001c0001t0014g0122a0001c0001t0014g0123 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2959-299G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715128 | ||||||
| chr12:98715220
|
G | T | 168 | a0001c0001t0001g0121a0001c0001t0002g0209a0001c0001t0002g0221others(165): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.2959-207G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715220 | ||||||
| chr12:98715226
|
CATGGTGT others(36): Show |
C | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2959-198_2959-156d others(45): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715226 | |||||
| chr12:98715234
|
G | T | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2959-193G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715234 | ||||||
| chr12:98715235
|
C | CAT | 13 | a0001c0001t0001g0246a0001c0001t0001g0283a0001c0001t0002g0319others(10): Show | 13 | HG00642.hp2 HG01258.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.2959-147_2959-146d others(4): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
C | CATAT | 4 | a0001c0001t0001g0240a0001c0001t0003g0172a0001c0001t0003g0175others(1): Show | 4 | HG02630.hp1 NA18945.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.2959-149_2959-146d others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
C | CATATAT | 6 | a0001c0001t0001g0002a0001c0001t0001g0232a0001c0001t0001g0276others(3): Show | 7 | HG02809.hp1 HG02976.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.2959-151_2959-146d others(8): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
C | CATATATA others(1): Show |
10 | a0001c0001t0001g0121a0001c0001t0001g0230a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02723.hp1 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.2959-153_2959-146d others(10): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
C | CATATATA others(3): Show |
5 | a0001c0001t0002g0315a0001c0001t0004g0190a0001c0001t0004g0192others(2): Show | 5 | HG00738.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2959-155_2959-146d others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
C | CATATATA others(5): Show |
1 | a0001c0001t0015g0129 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2959-157_2959-146d others(14): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
C | CATATATA others(11): Show |
1 | a0001c0001t0003g0131 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2959-163_2959-146d others(20): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
C | CATATATA others(15): Show |
1 | a0001c0001t0003g0161 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2959-167_2959-146d others(24): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
CAT | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0025others(60): Show | 64 | HG00408.hp2 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.2959-147_2959-146d others(4): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
CATAT | C | 30 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0100others(27): Show | 30 | HG00438.hp2 HG00558.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2959-149_2959-146d others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
CATATAT | C | 26 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0035others(23): Show | 26 | HG00280.hp2 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.2959-151_2959-146d others(8): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
CATATATA others(1): Show |
C | 13 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0039others(10): Show | 13 | HG00280.hp1 HG01099.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.2959-153_2959-146d others(10): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
CATATATA others(3): Show |
C | 8 | a0001c0001t0001g0235a0001c0001t0001g0269a0001c0001t0012g0212others(5): Show | 8 | HG01361.hp2 HG01884.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2959-155_2959-146d others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
CATATATA others(5): Show |
C | 16 | a0001c0001t0001g0031a0001c0001t0001g0056a0001c0001t0001g0104others(13): Show | 16 | HG00140.hp1 HG02083.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.2959-157_2959-146d others(14): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
CATATATA others(7): Show |
C | 27 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0034others(24): Show | 28 | HG00544.hp2 HG00621.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.2959-159_2959-146d others(16): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
CATATATA others(9): Show |
C | 49 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(46): Show | 49 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.2959-161_2959-146d others(18): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
CATATATA others(11): Show |
C | 8 | a0001c0001t0001g0011a0001c0001t0001g0074a0001c0001t0005g0040others(5): Show | 8 | HG01081.hp1 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2959-163_2959-146d others(20): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
CATATATA others(13): Show |
C | 4 | a0001c0001t0001g0004a0001c0001t0001g0259a0001c0001t0024g0162others(1): Show | 4 | HG00741.hp1 HG02129.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2959-165_2959-146d others(22): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
CATATATA others(17): Show |
C | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2959-169_2959-146d others(26): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715235
|
CATATATA others(25): Show |
C | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2959-177_2959-146d others(34): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr12 | 98715235 | |||||
| chr12:98715248
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2959-179A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715248 | ||||||
| chr12:98715249
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2959-178T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715249 | ||||||
| chr12:98715268
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02055.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2959-159A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715268 | ||||||
| chr12:98715280
|
A | G | 3 | a0001c0001t0002g0333a0001c0001t0002g0345a0001c0001t0006g0222 | 3 | HG02293.hp1 NA18948.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.2959-147A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715280 | ||||||
| chr12:98715281
|
T | A | 3 | a0001c0001t0002g0333a0001c0001t0002g0345a0001c0001t0006g0222 | 3 | HG02293.hp1 NA18948.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.2959-146T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715281 | ||||||
| chr12:98715281
|
T | TATATATA others(15): Show |
1 | a0001c0001t0002g0330 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2959-146_2959-145i others(24): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715281 | ||||||
| chr12:98715281
|
T | TATATATA others(13): Show |
3 | a0001c0001t0002g0325a0001c0001t0006g0124a0001c0001t0006g0138 | 3 | HG02698.hp1 NA18991.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2959-146_2959-145i others(22): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715281 | ||||||
| chr12:98715281
|
T | TATATATA others(11): Show |
1 | a0001c0001t0002g0339 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2959-146_2959-145i others(20): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715281 | ||||||
| chr12:98715281
|
T | TATATATA others(9): Show |
2 | a0001c0001t0002g0341a0001c0001t0002g0347 | 2 | HG02080.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2959-146_2959-145i others(18): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715281 | ||||||
| chr12:98715281
|
T | TATATATA others(7): Show |
5 | a0001c0001t0002g0324a0001c0001t0002g0332a0001c0001t0002g0344others(2): Show | 5 | HG00621.hp2 HG02135.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.2959-146_2959-145i others(16): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715281 | ||||||
| chr12:98715281
|
T | TATATATA others(5): Show |
9 | a0001c0001t0002g0314a0001c0001t0002g0326a0001c0001t0002g0328others(6): Show | 9 | HG00408.hp1 HG03239.hp2 HG04199.hp2 others(6): Show |
intron_variant | MODIFIER | c.2959-146_2959-145i others(14): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715281 | ||||||
| chr12:98715281
|
T | TATATATA others(3): Show |
16 | a0001c0001t0002g0209a0001c0001t0002g0327a0001c0001t0002g0331others(13): Show | 16 | HG01257.hp1 HG01346.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.2959-146_2959-145i others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715281 | ||||||
| chr12:98715281
|
T | TATGTATA others(3): Show |
1 | a0001c0001t0006g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2959-146_2959-145i others(12): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 21/26 | chr12 | 98715281 | ||||||
| chr12:98715645
|
A | C | 53 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.3084+93A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98715645 | ||||||
| chr12:98715757
|
GA | G | 24 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(21): Show | 24 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.3084+207delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr12 | 98715757 | |||||
| chr12:98715761
|
G | T | 6 | a0001c0001t0036g0300a0001c0001t0037g0299a0001c0004t0007g0225others(3): Show | 6 | HG01081.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3084+209G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98715761 | ||||||
| chr12:98716069
|
A | C | 1 | a0001c0001t0014g0293 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3084+517A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98716069 | ||||||
| chr12:98716132
|
C | T | 1 | a0001c0001t0001g0363 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3084+580C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98716132 | ||||||
| chr12:98716277
|
C | A | 5 | a0001c0002t0001g0355a0001c0002t0023g0309a0001c0002t0032g0217others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3084+725C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98716277 | ||||||
| chr12:98716282
|
C | G | 57 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(54): Show | 57 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.3084+730C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98716282 | ||||||
| chr12:98716423
|
A | G | 63 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.3084+871A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98716423 | ||||||
| chr12:98716669
|
T | C | 168 | a0001c0001t0001g0121a0001c0001t0002g0209a0001c0001t0002g0221others(165): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.3084+1117T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98716669 | ||||||
| chr12:98716915
|
G | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.3084+1363G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98716915 | ||||||
| chr12:98717036
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0108others(2): Show | 5 | HG03098.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3084+1484T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717036 | ||||||
| chr12:98717067
|
A | G | 1 | a0001c0001t0012g0218 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3084+1515A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717067 | ||||||
| chr12:98717115
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0119 | 3 | HG01071.hp2 HG02148.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.3084+1563G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717115 | ||||||
| chr12:98717119
|
C | T | 5 | a0001c0001t0001g0107a0001c0001t0013g0301a0001c0001t0013g0302others(2): Show | 5 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3084+1567C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717119 | ||||||
| chr12:98717136
|
G | A | 6 | a0001c0001t0036g0300a0001c0001t0037g0299a0001c0004t0007g0225others(3): Show | 6 | HG01081.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3084+1584G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717136 | ||||||
| chr12:98717155
|
C | A | 1 | a0001c0001t0013g0301 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3084+1603C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717155 | ||||||
| chr12:98717157
|
C | T | 1 | a0001c0001t0024g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3084+1605C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717157 | ||||||
| chr12:98717160
|
A | G | 1 | a0001c0001t0013g0301 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3084+1608A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717160 | ||||||
| chr12:98717163
|
T | C | 1 | a0001c0001t0013g0301 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3084+1611T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717163 | ||||||
| chr12:98717169
|
A | G | 1 | a0001c0001t0036g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3084+1617A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717169 | ||||||
| chr12:98717602
|
T | G | 15 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(12): Show | 15 | HG02257.hp2 HG02647.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.3084+2050T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717602 | ||||||
| chr12:98717612
|
G | A | 1 | a0001c0001t0024g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3084+2060G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717612 | ||||||
| chr12:98717617
|
C | A | 1 | a0001c0001t0036g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3084+2065C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717617 | ||||||
| chr12:98717932
|
C | T | 2 | a0001c0004t0007g0225a0001c0004t0007g0226 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3084+2380C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717932 | ||||||
| chr12:98717990
|
A | T | 1 | a0001c0001t0004g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3084+2438A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98717990 | ||||||
| chr12:98718280
|
C | T | 24 | a0001c0001t0002g0314a0001c0001t0002g0326a0001c0001t0002g0327others(21): Show | 24 | HG00323.hp2 HG01257.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3084+2728C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98718280 | ||||||
| chr12:98718302
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 159 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.3084+2750G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98718302 | ||||||
| chr12:98718545
|
A | G | 137 | a0001c0001t0001g0121a0001c0001t0002g0209a0001c0001t0002g0221others(134): Show | 137 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.3084+2993A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98718545 | ||||||
| chr12:98718648
|
T | C | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3084+3096T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98718648 | ||||||
| chr12:98718896
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0100a0001c0001t0001g0118 | 3 | HG00735.hp2 HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3084+3344C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98718896 | ||||||
| chr12:98718939
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0077 | 2 | HG00738.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.3084+3387T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98718939 | ||||||
| chr12:98718998
|
C | T | 1 | a0001c0001t0004g0185 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3084+3446C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98718998 | ||||||
| chr12:98719329
|
G | A | 1 | a0001c0001t0006g0171 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3084+3777G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98719329 | ||||||
| chr12:98719385
|
C | T | 1 | a0001c0001t0003g0175 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3085-3808C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98719385 | ||||||
| chr12:98719516
|
AT | A | 8 | a0001c0001t0001g0273a0001c0001t0004g0187a0001c0001t0008g0306others(5): Show | 8 | HG01891.hp2 HG02451.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.3085-3660delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr12 | 98719516 | |||||
| chr12:98719632
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3085-3561G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98719632 | ||||||
| chr12:98719780
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(108): Show | 112 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.3085-3413C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98719780 | ||||||
| chr12:98719882
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3085-3311T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98719882 | ||||||
| chr12:98720002
|
T | C | 1 | a0001c0001t0024g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3085-3191T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98720002 | ||||||
| chr12:98720008
|
C | T | 2 | a0001c0002t0023g0309a0001c0002t0032g0217 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3085-3185C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98720008 | ||||||
| chr12:98720514
|
C | A | 323 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(320): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.3085-2679C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98720514 | ||||||
| chr12:98720588
|
C | A | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3085-2605C>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98720588 | ||||||
| chr12:98720688
|
G | A | 1 | a0001c0001t0004g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3085-2505G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98720688 | ||||||
| chr12:98720691
|
T | C | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3085-2502T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98720691 | ||||||
| chr12:98720716
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3085-2477G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98720716 | ||||||
| chr12:98720741
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 4 | NA18612.hp2 NA18952.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3085-2452G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98720741 | ||||||
| chr12:98720860
|
A | G | 54 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(51): Show | 54 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.3085-2333A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98720860 | ||||||
| chr12:98720976
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.3085-2217G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98720976 | ||||||
| chr12:98720976
|
GA | G | 16 | a0001c0001t0004g0178a0001c0001t0004g0179a0001c0001t0004g0180others(13): Show | 16 | HG00280.hp2 HG00738.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.3085-2207delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr12 | 98720976 | |||||
| chr12:98720978
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.3085-2215A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98720978 | ||||||
| chr12:98720982
|
A | G | 10 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(7): Show | 10 | HG00735.hp1 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3085-2211A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98720982 | ||||||
| chr12:98720991
|
C | G | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3085-2202C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98720991 | ||||||
| chr12:98721018
|
T | C | 1 | a0001c0001t0027g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3085-2175T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98721018 | ||||||
| chr12:98721101
|
G | A | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3085-2092G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98721101 | ||||||
| chr12:98721111
|
A | G | 1 | a0001c0001t0003g0158 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3085-2082A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98721111 | ||||||
| chr12:98721441
|
G | A | 323 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(320): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.3085-1752G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98721441 | ||||||
| chr12:98721564
|
C | G | 1 | a0001c0001t0001g0260 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3085-1629C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98721564 | ||||||
| chr12:98721829
|
G | T | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3085-1364G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98721829 | ||||||
| chr12:98721883
|
G | A | 194 | a0001c0001t0001g0036a0001c0001t0001g0253a0001c0001t0001g0254others(191): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.3085-1310G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98721883 | ||||||
| chr12:98721886
|
T | C | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3085-1307T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98721886 | ||||||
| chr12:98721890
|
C | G | 72 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(69): Show | 72 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.3085-1303C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98721890 | ||||||
| chr12:98721979
|
G | A | 13 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(10): Show | 13 | HG02647.hp2 HG02717.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.3085-1214G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98721979 | ||||||
| chr12:98722061
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0108others(2): Show | 5 | HG03098.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3085-1132C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98722061 | ||||||
| chr12:98722076
|
C | T | 9 | a0001c0001t0006g0124a0001c0001t0006g0160a0001c0001t0006g0163others(6): Show | 9 | HG00323.hp2 HG01257.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.3085-1117C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98722076 | ||||||
| chr12:98722124
|
C | T | 1 | a0001c0001t0005g0058 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3085-1069C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98722124 | ||||||
| chr12:98722566
|
T | C | 7 | a0001c0001t0001g0035a0001c0001t0009g0042a0001c0001t0009g0070others(4): Show | 7 | HG01891.hp1 HG02486.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3085-627T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98722566 | ||||||
| chr12:98722677
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3085-516C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98722677 | ||||||
| chr12:98722683
|
T | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0049 | 3 | HG00621.hp1 NA18961.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3085-510T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98722683 | ||||||
| chr12:98722712
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3085-481A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98722712 | ||||||
| chr12:98722743
|
G | A | 2 | a0002c0003t0007g0353a0002c0003t0007g0354 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3085-450G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98722743 | ||||||
| chr12:98722792
|
G | T | 1 | a0001c0001t0001g0238 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3085-401G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98722792 | ||||||
| chr12:98722905
|
G | GT | 22 | a0001c0001t0001g0098a0001c0001t0008g0308a0001c0001t0008g0310others(19): Show | 22 | HG00735.hp1 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.3085-277dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr12 | 98722905 | |||||
| chr12:98722929
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3085-264A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98722929 | ||||||
| chr12:98723019
|
G | A | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3085-174G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98723019 | ||||||
| chr12:98723066
|
C | G | 3 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303 | 3 | HG01884.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3085-127C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98723066 | ||||||
| chr12:98723141
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(108): Show | 112 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.3085-52A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 22/26 | chr12 | 98723141 | ||||||
| chr12:98723492
|
TGTTA | T | 8 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0001g0232others(5): Show | 8 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.3205-144_3205-141d others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr12 | 98723492 | |||||
| chr12:98723619
|
G | GT | 70 | a0001c0001t0001g0056a0001c0001t0001g0119a0001c0001t0001g0121others(67): Show | 70 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(67): Show |
splice_region_variant&intron_variant | LOW | c.3205-4dupT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr12 | 98723619 | |||||
| chr12:98723619
|
GT | G | 55 | a0001c0001t0001g0077a0001c0001t0002g0209a0001c0001t0002g0221others(52): Show | 55 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(52): Show |
splice_region_variant&intron_variant | LOW | c.3205-4delT | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr12 | 98723619 | |||||
| chr12:98723624
|
T | G | 15 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(12): Show | 15 | HG02257.hp2 HG02647.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.3205-15T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 23/26 | chr12 | 98723624 | ||||||
| chr12:98723773
|
A | G | 2 | a0001c0001t0005g0083a0001c0001t0005g0096 | 2 | NA18945.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3330+9A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98723773 | ||||||
| chr12:98723777
|
A | G | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3330+13A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98723777 | ||||||
| chr12:98723824
|
C | T | 1 | a0001c0001t0003g0168 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3330+60C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98723824 | ||||||
| chr12:98724036
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3330+272T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98724036 | ||||||
| chr12:98724281
|
A | G | 8 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(5): Show | 8 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.3330+517A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98724281 | ||||||
| chr12:98724348
|
G | T | 1 | a0001c0001t0001g0240 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3330+584G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98724348 | ||||||
| chr12:98724660
|
T | G | 4 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0017g0202others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.3331-755T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98724660 | ||||||
| chr12:98724730
|
G | A | 54 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(51): Show | 54 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.3331-685G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98724730 | ||||||
| chr12:98724735
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(109): Show | 113 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.3331-680C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98724735 | ||||||
| chr12:98724736
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(109): Show | 113 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.3331-679C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98724736 | ||||||
| chr12:98724737
|
T | TA | 112 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(109): Show | 113 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.3331-678_3331-677i others(3): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98724737 | ||||||
| chr12:98724738
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(109): Show | 113 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.3331-677G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98724738 | ||||||
| chr12:98724894
|
GA | G | 93 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(90): Show | 93 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.3331-511delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr12 | 98724894 | |||||
| chr12:98724969
|
G | C | 16 | a0001c0001t0004g0126a0001c0001t0004g0176a0001c0001t0004g0177others(13): Show | 16 | HG00639.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3331-446G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98724969 | ||||||
| chr12:98725389
|
G | A | 1 | a0001c0001t0009g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3331-26G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 24/26 | chr12 | 98725389 | ||||||
| chr12:98725562
|
G | A | 22 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0257others(19): Show | 22 | HG00140.hp1 HG00544.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.3456+22G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98725562 | ||||||
| chr12:98725576
|
T | A | 1 | a0001c0001t0003g0161 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3456+36T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98725576 | ||||||
| chr12:98725577
|
T | C | 12 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(9): Show | 12 | HG00735.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3456+37T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98725577 | ||||||
| chr12:98725606
|
G | A | 4 | a0001c0001t0015g0127a0001c0001t0015g0128a0001c0001t0015g0129others(1): Show | 4 | HG01891.hp2 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3456+66G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98725606 | ||||||
| chr12:98725640
|
C | G | 2 | a0001c0001t0010g0292a0001c0001t0010g0296 | 2 | NA18940.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.3456+100C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98725640 | ||||||
| chr12:98725737
|
A | T | 1 | a0001c0001t0027g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3456+197A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98725737 | ||||||
| chr12:98726052
|
T | C | 1 | a0001c0004t0007g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3456+512T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98726052 | ||||||
| chr12:98726055
|
T | G | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3456+515T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98726055 | ||||||
| chr12:98726109
|
T | C | 1 | a0001c0004t0007g0225 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3456+569T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98726109 | ||||||
| chr12:98726139
|
C | G | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.3456+599C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98726139 | ||||||
| chr12:98726200
|
T | A | 1 | a0001c0002t0001g0355 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3456+660T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98726200 | ||||||
| chr12:98726211
|
T | A | 5 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(2): Show | 5 | NA18940.hp2 NA18952.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.3456+671T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98726211 | ||||||
| chr12:98726292
|
T | G | 69 | a0001c0001t0001g0121a0001c0001t0003g0125a0001c0001t0003g0130others(66): Show | 69 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.3456+752T>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98726292 | ||||||
| chr12:98726684
|
T | A | 1 | a0001c0001t0003g0161 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3457-489T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98726684 | ||||||
| chr12:98726965
|
G | A | 1 | a0001c0004t0007g0225 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3457-208G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 25/26 | chr12 | 98726965 | ||||||
| chr12:98727376
|
A | G | 1 | a0001c0004t0007g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3600+60A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727376 | ||||||
| chr12:98727546
|
CA | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.3600+247delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr12 | 98727546 | |||||
| chr12:98727581
|
T | A | 1 | a0007c0011t0025g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3600+265T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727581 | ||||||
| chr12:98727770
|
G | A | 324 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.3600+454G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727770 | ||||||
| chr12:98727785
|
A | C | 37 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(34): Show | 37 | HG00408.hp2 HG00558.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.3600+469A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727785 | ||||||
| chr12:98727810
|
A | G | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG00140.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.3600+494A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727810 | ||||||
| chr12:98727811
|
T | C | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG00140.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.3600+495T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727811 | ||||||
| chr12:98727865
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0289a0001c0001t0001g0290 | 4 | HG00642.hp1 HG00733.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3600+549C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727865 | ||||||
| chr12:98727901
|
A | G | 22 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(19): Show | 22 | HG00735.hp1 HG01081.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3600+585A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727901 | ||||||
| chr12:98727962
|
A | T | 2 | a0001c0001t0002g0338a0001c0001t0007g0250 | 2 | HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.3600+646A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727962 | ||||||
| chr12:98727966
|
A | T | 17 | a0001c0001t0001g0078a0001c0001t0001g0287a0001c0001t0001g0288others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.3600+650A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727966 | ||||||
| chr12:98727966
|
AAATT | A | 7 | a0001c0001t0001g0260a0001c0001t0013g0301a0001c0001t0013g0302others(4): Show | 7 | HG01109.hp1 HG01192.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.3600+669_3600+672d others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr12 | 98727966 | |||||
| chr12:98727966
|
AAATTAAT others(1): Show |
A | 13 | a0001c0001t0010g0291a0001c0001t0010g0292a0001c0001t0010g0295others(10): Show | 13 | HG02647.hp2 HG02717.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.3600+665_3600+672d others(10): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr12 | 98727966 | |||||
| chr12:98727970
|
T | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.3600+654T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727970 | ||||||
| chr12:98727974
|
T | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0052others(25): Show | 28 | HG00544.hp1 HG00735.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.3600+658T>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98727974 | ||||||
| chr12:98727990
|
AAAAT | A | 72 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0003g0131others(69): Show | 72 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.3600+682_3600+685d others(6): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr12 | 98727990 | |||||
| chr12:98728005
|
G | T | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.3600+689G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98728005 | ||||||
| chr12:98728188
|
G | A | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.3600+872G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98728188 | ||||||
| chr12:98728195
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0108others(2): Show | 5 | HG03098.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3600+879T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98728195 | ||||||
| chr12:98728319
|
C | T | 4 | a0001c0001t0015g0127a0001c0001t0015g0128a0001c0001t0015g0129others(1): Show | 4 | HG01891.hp2 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3600+1003C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98728319 | ||||||
| chr12:98728546
|
G | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.3600+1230G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98728546 | ||||||
| chr12:98728557
|
TA | T | 164 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(161): Show | 164 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.3600+1247delA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr12 | 98728557 | |||||
| chr12:98728602
|
T | C | 1 | a0001c0001t0012g0210 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3600+1286T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98728602 | ||||||
| chr12:98728709
|
C | T | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3600+1393C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98728709 | ||||||
| chr12:98728908
|
T | C | 14 | a0001c0001t0008g0305a0001c0001t0008g0306a0001c0001t0008g0308others(11): Show | 14 | HG00735.hp1 HG01081.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.3600+1592T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98728908 | ||||||
| chr12:98728925
|
C | T | 1 | a0001c0001t0005g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3600+1609C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98728925 | ||||||
| chr12:98729160
|
C | T | 1 | a0001c0001t0005g0082 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3600+1844C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98729160 | ||||||
| chr12:98729220
|
A | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0108others(2): Show | 5 | HG03098.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3600+1904A>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98729220 | ||||||
| chr12:98729232
|
A | G | 1 | a0001c0002t0001g0355 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3600+1916A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98729232 | ||||||
| chr12:98729249
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3600+1933C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98729249 | ||||||
| chr12:98729533
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3600+2217G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98729533 | ||||||
| chr12:98729631
|
A | G | 2 | a0003c0005t0007g0219a0003c0005t0007g0220 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3600+2315A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98729631 | ||||||
| chr12:98729659
|
A | C | 1 | a0001c0001t0001g0035 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3600+2343A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98729659 | ||||||
| chr12:98729910
|
G | T | 4 | a0001c0001t0015g0127a0001c0001t0015g0128a0001c0001t0015g0129others(1): Show | 4 | HG01891.hp2 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3601-2510G>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98729910 | ||||||
| chr12:98730021
|
GATATCCC others(4): Show |
G | 1 | a0001c0001t0004g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3601-2396_3601-238 others(15): Show |
APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr12 | 98730021 | |||||
| chr12:98730128
|
A | C | 6 | a0001c0001t0002g0209a0001c0001t0002g0328a0001c0001t0002g0329others(3): Show | 6 | HG00408.hp1 HG02015.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.3601-2292A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98730128 | ||||||
| chr12:98730366
|
C | G | 1 | a0001c0001t0001g0361 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3601-2054C>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98730366 | ||||||
| chr12:98730819
|
T | TA | 69 | a0001c0001t0001g0121a0001c0001t0003g0125a0001c0001t0003g0130others(66): Show | 69 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.3601-1599dupA | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr12 | 98730819 | |||||
| chr12:98730962
|
G | A | 55 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(52): Show | 55 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.3601-1458G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98730962 | ||||||
| chr12:98731007
|
A | G | 1 | a0001c0001t0027g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3601-1413A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98731007 | ||||||
| chr12:98731078
|
T | C | 1 | a0001c0001t0010g0291 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3601-1342T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98731078 | ||||||
| chr12:98731131
|
G | C | 4 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0020g0351others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.3601-1289G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98731131 | ||||||
| chr12:98731133
|
A | G | 1 | a0001c0001t0024g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3601-1287A>G | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98731133 | ||||||
| chr12:98731134
|
C | T | 55 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0002g0314others(52): Show | 55 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.3601-1286C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98731134 | ||||||
| chr12:98731300
|
T | C | 8 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(5): Show | 8 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.3601-1120T>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98731300 | ||||||
| chr12:98731373
|
G | A | 1 | a0001c0001t0003g0158 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3601-1047G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98731373 | ||||||
| chr12:98731419
|
A | C | 4 | a0001c0001t0013g0301a0001c0001t0013g0302a0001c0001t0013g0303others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3601-1001A>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98731419 | ||||||
| chr12:98731423
|
G | C | 1 | a0001c0001t0007g0250 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3601-997G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98731423 | ||||||
| chr12:98731586
|
C | T | 2 | a0001c0001t0036g0300a0001c0001t0037g0299 | 2 | HG01081.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.3601-834C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98731586 | ||||||
| chr12:98731855
|
C | T | 5 | a0001c0001t0012g0210a0001c0001t0013g0301a0001c0001t0013g0302others(2): Show | 5 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3601-565C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98731855 | ||||||
| chr12:98731856
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3601-564G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98731856 | ||||||
| chr12:98731870
|
G | A | 4 | a0001c0001t0015g0127a0001c0001t0015g0128a0001c0001t0015g0129others(1): Show | 4 | HG01891.hp2 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3601-550G>A | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98731870 | ||||||
| chr12:98732290
|
C | T | 5 | a0001c0001t0001g0240a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG02132.hp1 HG02155.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.3601-130C>T | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98732290 | ||||||
| chr12:98732326
|
G | C | 1 | a0001c0001t0001g0357 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3601-94G>C | APAF1 | ENSG00000120868.14 | transcript | ENST00000551964.6 | protein_coding | 26/26 | chr12 | 98732326 |